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array:24 [ "pii" => "S2173578614001061" "issn" => "21735786" "doi" => "10.1016/j.acuroe.2014.06.004" "estado" => "S300" "fechaPublicacion" => "2014-09-01" "aid" => "643" "copyright" => "AEU" "copyrightAnyo" => "2014" "documento" => "article" "crossmark" => 0 "subdocumento" => "ssu" "cita" => "Actas Urol Esp. 2014;38:429-37" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 394 "formatos" => array:3 [ "EPUB" => 11 "HTML" => 256 "PDF" => 127 ] ] "Traduccion" => array:1 [ "es" => array:19 [ "pii" => "S0210480614000680" "issn" => "02104806" "doi" => "10.1016/j.acuro.2014.02.017" "estado" => "S300" "fechaPublicacion" => "2014-09-01" "aid" => "643" "copyright" => "AEU" "documento" => "article" "crossmark" => 0 "subdocumento" => "ssu" "cita" => "Actas Urol Esp. 2014;38:429-37" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 720 "formatos" => array:3 [ "EPUB" => 10 "HTML" => 545 "PDF" => 165 ] ] "es" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Artículo Original</span>" "titulo" => "Los polifenoles del vino ejercen su efecto antineoplásico sobre la línea celular PC-3 andrógeno resistente a través de la inhibición de la actividad transcripcional del promotor de COX-2 mediada por NF-kβ" "tienePdf" => "es" "tieneTextoCompleto" => "es" "tieneResumen" => array:2 [ 0 => "es" 1 => "en" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "429" "paginaFinal" => "437" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Wine Polyphenols Exert Antineoplasic Effect on Androgen Resistant PC-3 Cell Line Through the Inhibition of the Transcriptional Activity of COX-2 Promoter Mediated by NF-kβ" ] ] "contieneResumen" => array:2 [ "es" => true "en" => true ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0030" "etiqueta" => "Figura 6" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr6.jpeg" "Alto" => 2098 "Ancho" => 1638 "Tamanyo" => 90865 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">Inducción de la apoptosis por los polifenoles en las células de PC-3 determinadas por la actividad de la caspasa 3/7 en las células de control y tratadas. Todos los compuestos indujeron la apoptosis a las 48<span class="elsevierStyleHsp" style=""></span>h, aunque a un ritmo diferente: ácido tánico 3,5, ácido gálico 1,7, quercetina 1,6 y resveratrol 42,5 veces en comparación con el control (A). Las pequeñas diferencias se pueden apreciar en detalle (B).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "A. Ferruelo, M.M. de las Heras, C. Redondo, F. Ramón de Fata, I. Romero, J.C. Angulo" "autores" => array:6 [ 0 => array:2 [ "nombre" => "A." "apellidos" => "Ferruelo" ] 1 => array:2 [ "nombre" => "M.M." "apellidos" => "de las Heras" ] 2 => array:2 [ "nombre" => "C." "apellidos" => "Redondo" ] 3 => array:2 [ "nombre" => "F." "apellidos" => "Ramón de Fata" ] 4 => array:2 [ "nombre" => "I." "apellidos" => "Romero" ] 5 => array:2 [ "nombre" => "J.C." "apellidos" => "Angulo" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S2173578614001061" "doi" => "10.1016/j.acuroe.2014.06.004" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173578614001061?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0210480614000680?idApp=UINPBA00004N" "url" => "/02104806/0000003800000007/v1_201408240357/S0210480614000680/v1_201408240357/es/main.assets" ] ] "itemSiguiente" => array:18 [ "pii" => "S2173578614001231" "issn" => "21735786" "doi" => "10.1016/j.acuroe.2014.06.006" "estado" => "S300" "fechaPublicacion" => "2014-09-01" "aid" => "630" "copyright" => "AEU" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Actas Urol Esp. 2014;38:438-44" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 668 "formatos" => array:3 [ "EPUB" => 12 "HTML" => 541 "PDF" => 115 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original article</span>" "titulo" => "Prostate anatomy in motheaten viable (<span class="elsevierStyleItalic">me</span><span class="elsevierStyleSup"><span class="elsevierStyleItalic">v</span></span>) mice with mutations in the protein tyrosine phosphatase SHP-1" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "438" "paginaFinal" => "444" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Anatomía de la próstata en ratones <span class="elsevierStyleItalic">motheaten viable (me</span><span class="elsevierStyleSup"><span class="elsevierStyleItalic"><span class="elsevierStyleBold">v</span></span></span><span class="elsevierStyleItalic">)</span> con mutaciones en el gen de la proteína tirosina fosfatasa SHP-1" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 2090 "Ancho" => 1626 "Tamanyo" => 785400 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Completely cut histological section of the prostate and seminal complex. Absence of seminal vesicles and a relatively decreased size of the prostatic structures, with normal urinary bladder, are confirmed in <span class="elsevierStyleItalic">me<span class="elsevierStyleSup">v</span></span> mice.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "A. García-Tello, J.C. Angulo, J. Rodriguez-Ubreva, G. Andrés, J.I. López, M. Sánchez-Chapado, P. López-Ruiz, B. Colás" "autores" => array:8 [ 0 => array:2 [ "nombre" => "A." "apellidos" => "García-Tello" ] 1 => array:2 [ "nombre" => "J.C." "apellidos" => "Angulo" ] 2 => array:2 [ "nombre" => "J." "apellidos" => "Rodriguez-Ubreva" ] 3 => array:2 [ "nombre" => "G." "apellidos" => "Andrés" ] 4 => array:2 [ "nombre" => "J.I." "apellidos" => "López" ] 5 => array:2 [ "nombre" => "M." "apellidos" => "Sánchez-Chapado" ] 6 => array:2 [ "nombre" => "P." "apellidos" => "López-Ruiz" ] 7 => array:2 [ "nombre" => "B." "apellidos" => "Colás" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173578614001231?idApp=UINPBA00004N" "url" => "/21735786/0000003800000007/v1_201408240422/S2173578614001231/v1_201408240422/en/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S2173578614001048" "issn" => "21735786" "doi" => "10.1016/j.acuroe.2014.06.002" "estado" => "S300" "fechaPublicacion" => "2014-09-01" "aid" => "623" "copyright" => "AEU" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Actas Urol Esp. 2014;38:421-8" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 437 "formatos" => array:3 [ "EPUB" => 11 "HTML" => 285 "PDF" => 141 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original article</span>" "titulo" => "Preservation of the internal vesical sphincter and proximal urethra during retropubic radical prostatectomy may improve earlier recovery of continence in selected patients" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "421" "paginaFinal" => "428" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "La preservación del esfínter interno vesical y la uretra proximal durante la prostatectomía radical retropúbica puede mejorar la recuperación temprana de la continencia en pacientes seleccionados" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 802 "Ancho" => 1000 "Tamanyo" => 163429 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Standardization of the ring-shaped bladder sphincter and longitudinal smooth muscle of the proximal urethra during dissection of dorsal aspect of the prostate and the neck of the bladder.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "E. Brunocilla, R. Schiavina, M. Borghesi, C. Pultrone, V. Vagnoni, M.S. Rossi, M. Cevenini, L. Bianchi, E. Molinaroli, G. Gentile, G. Martorana" "autores" => array:11 [ 0 => array:2 [ "nombre" => "E." "apellidos" => "Brunocilla" ] 1 => array:2 [ "nombre" => "R." "apellidos" => "Schiavina" ] 2 => array:2 [ "nombre" => "M." "apellidos" => "Borghesi" ] 3 => array:2 [ "nombre" => "C." "apellidos" => "Pultrone" ] 4 => array:2 [ "nombre" => "V." "apellidos" => "Vagnoni" ] 5 => array:2 [ "nombre" => "M.S." "apellidos" => "Rossi" ] 6 => array:2 [ "nombre" => "M." "apellidos" => "Cevenini" ] 7 => array:2 [ "nombre" => "L." "apellidos" => "Bianchi" ] 8 => array:2 [ "nombre" => "E." "apellidos" => "Molinaroli" ] 9 => array:2 [ "nombre" => "G." "apellidos" => "Gentile" ] 10 => array:2 [ "nombre" => "G." "apellidos" => "Martorana" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0210480614000357" "doi" => "10.1016/j.acuro.2013.12.010" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0210480614000357?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173578614001048?idApp=UINPBA00004N" "url" => "/21735786/0000003800000007/v1_201408240422/S2173578614001048/v1_201408240422/en/main.assets" ] "en" => array:20 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original article</span>" "titulo" => "Wine polyphenols exert antineoplasic effect on androgen resistant PC-3 cell line through the inhibition of the transcriptional activity of COX-2 promoter mediated by NF-κβ" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "429" "paginaFinal" => "437" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "A. Ferruelo, M.M. de las Heras, C. Redondo, F. Ramón de Fata, I. Romero, J.C. Angulo" "autores" => array:6 [ 0 => array:3 [ "nombre" => "A." "apellidos" => "Ferruelo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 1 => array:3 [ "nombre" => "M.M." "apellidos" => "de las Heras" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 2 => array:3 [ "nombre" => "C." "apellidos" => "Redondo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 3 => array:3 [ "nombre" => "F." "apellidos" => "Ramón de Fata" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 4 => array:3 [ "nombre" => "I." "apellidos" => "Romero" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 5 => array:4 [ "nombre" => "J.C." "apellidos" => "Angulo" "email" => array:1 [ 0 => "javier.angulo@salud.madrid.org" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Unidad de Investigación, Fundación para la Investigación Biomédica del Hospital Universitario de Getafe, Madrid, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Urología, Hospital Universitario de Getafe, Departamento Clínico, Facultad de Ciencias Biomédicas, Universidad Europea de Madrid, Madrid, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Los polifenoles del vino ejercen su efecto antineoplásico sobre la línea celular PC-3 andrógeno resistente a través de la inhibición de la actividad transcripcional del promotor de COX-2 mediada por NF-κβ" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0030" "etiqueta" => "Figure 6" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr6.jpeg" "Alto" => 2149 "Ancho" => 1638 "Tamanyo" => 91843 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Induction of apoptosis by polyphenols on PC-3 cells determined by caspase 3/7 activity in control and treated cells. All compounds induced apoptosis at 48<span class="elsevierStyleHsp" style=""></span>h, although at a different rate: tannic acid 3.5, gallic acid 1.7, quercetin 1.6 and resveratrol 42.5 times compared to control (A). Minor differences can be appreciated in detail (B).</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Epidemiological studies provide rather consistent evidence that a diet which has a high content of fruits and vegetables reduces the risk for several types of cancer.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> However, the components of these nutrients that exert this protective effect and the precise mechanism by which they exert these effects are not known with certainty. Prostate cancer (PCa) remains a considerable health problem for men around the world. There is a large body of literature devoted to describe the potential chemopreventive or chemotherapeutic effect of certain phytochemicals in red wine polyphenols, including enhanced apoptosis, growth arrest, modification of the cell cycle, inhibition of DNA synthesis, and modulation expression of enzymes, such as cyclooxygenases or prostaglandin H2 synthase (COXs).<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2–5</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Polyphenolic compounds constitute one of the largest and most ubiquitous group of phytochemicals. These compounds, especially flavonoids and phenolic acids, are an import part of human diet.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,3</span></a> The biochemical properties, intake, and bioavailability of different polyphenolic compounds that have been reviewed for this topic are of particular interest in the issue of prostate cancer chemoprevention and/or modulation of therapies.<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6–8</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">There are two isoforms of COX that catalyze the formation of prostaglandins (PG) from arachidonic acid. Whereas COX-1 is a housekeeping gene that is expressed constitutively and is generally responsible for the production of PGs under physiological conditions, COX-2 is a highly inducible gene by different stimuli. Furthermore, COX-2 is thought to be the isoform responsible for the production of pro-inflammatory PGs and it is very important for tumorigenesis.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Cyclooxygenase-2 (COX-2) is considered a potential target for cancer therapy, because COX-2 levels are elevated in the majority of human tumors compared to corresponding normal tissues. There are different possible mechanisms that could account for the relation between COX-2 and cancer. Increased levels of PGs and COX-2 activity have been detected in multiple epithelial cancers (<span class="elsevierStyleItalic">e.g.</span>, lung, colon, prostate),<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10,11</span></a> and especially PGE<span class="elsevierStyleInf">2</span> can affect and increases cell proliferation and invasiveness, promoting angiogenesis and inhibiting apoptosis in malignant cells.</p><p id="par0025" class="elsevierStylePara elsevierViewall">Phorbol esters such as phorbol 12-myristate 13-acetate (PMA) function as tumor promoters and have been reported to modulate diverse cellular responses including cell growth, programmed cell death, differentiation, and gene transcription. It has been established that besides PMA, cytokines and lipopolysaccharide also upregulate COX-2 expression.<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">12–14</span></a> We have demonstrated that regulation of androgen receptor (AR) transcription mediates the antiproliferative effect of resveratrol and other wine polyphenols in androgen-sensitive LNCaP cell line.<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15,16</span></a> Now we intend to study <span class="elsevierStyleItalic">in vitro</span> the effects of these compounds in castration-resistant PCa and the mechanisms involved.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Materials and methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Materials</span><p id="par0030" class="elsevierStylePara elsevierViewall">PMA and polyphenolic compounds (tannic acid, gallic acid, quercetin and resveratrol) were purchased from Sigma–Aldrich (St. Louis, MO, USA) and dissolved in ethanol at stock concentration and stored at −20<span class="elsevierStyleHsp" style=""></span>°C. Final concentrations used for different experiments were prepared by diluting the stock with RPMI before use. Culture plastic was obtained from Corning-Costar (NY, USA). RPMI-1640 medium with 100<span class="elsevierStyleHsp" style=""></span>U/ml penicillin G, 0.1<span class="elsevierStyleHsp" style=""></span>mg/ml streptomycin, 50<span class="elsevierStyleHsp" style=""></span>μg/ml gentamicin, and 2<span class="elsevierStyleHsp" style=""></span>mM <span class="elsevierStyleSmallCaps">l</span>-glutamine were from Gibco BRL (Paisley, UK). Fetal bovine serum (FBS), Phosphate-buffered saline (PBS) and trypsin-ethylenediamine tetraacetate (EDTA) 0.025% were from Biological Industries (Beit-Hamek, Israel), Amresco (Solon, OH, USA), and Gibco BRM (Paisley, UK), respectively. MMLV reverse transcriptase was from Sigma–Aldrich (St. Louis, MO, USA).</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Cell culture and treatments</span><p id="par0035" class="elsevierStylePara elsevierViewall">The androgen-insensitive PC-3 cell line was obtained from the American type cultura collection (ATCC, Rockville, MD). Cells were maintained in RPMI 1640 (Gibco BRL, Spain) supplemented with 5% heat-inactivated fetal bovine serum (FCS, LINUS, Spain). Cells were cultured in a humidified atmosphere of 95% air and 5% CO<span class="elsevierStyleInf">2</span> at 37<span class="elsevierStyleHsp" style=""></span>°C and they were grown at 60–70% confluence, trypsinized with 0.05% trypsin-2<span class="elsevierStyleHsp" style=""></span>mM EDTA (Gibco BRL, Spain), and plated for experimental use. For experiments, the cells were treated with or without PMA (50<span class="elsevierStyleHsp" style=""></span>μg/ml) and 10<span class="elsevierStyleHsp" style=""></span>M of tannic acid, gallic acid, quercetin, and resveratrol or vehicle (ethanol 0.01%) for 24<span class="elsevierStyleHsp" style=""></span>h for mRNA expression and transfection assay, and for 48<span class="elsevierStyleHsp" style=""></span>h to study the effect of polyphenols on PGE<span class="elsevierStyleInf">2</span> secretion and apoptosis in PC-3 cells.</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">RNA extraction and real-time PCR for COX-2 expressions</span><p id="par0040" class="elsevierStylePara elsevierViewall">Total RNA from cell samples was obtained using RNeasy<span class="elsevierStyleSup">®</span> Mini kit, from Qiagen (Valencia, CA, USA) following the manufacturer's instructions. Yield of RNA was determined spectrophotometrically at 260/280<span class="elsevierStyleHsp" style=""></span>nm and density (OD<span class="elsevierStyleInf">260</span>/OD<span class="elsevierStyleInf">280</span>) ratios were measured to ensure the quality of the isolated RNA using ND-100 spectrophotometer (Nanodrop Technology). The average ratio was 1.8 to 2.1 for all samples. For RT, an aliquot containing 1–2<span class="elsevierStyleHsp" style=""></span>μg of total RNA from each sample was used for first-strand cDNA in a final volume of 20–40<span class="elsevierStyleHsp" style=""></span>l using 0.75<span class="elsevierStyleHsp" style=""></span>μl (0.5<span class="elsevierStyleHsp" style=""></span>mg) of random primers (Promega, Madison, WI) and 0.5<span class="elsevierStyleHsp" style=""></span>μl (12.5<span class="elsevierStyleHsp" style=""></span>mmol/L) dNTPs mixture (Ecogen, Spain), incubated at 70<span class="elsevierStyleHsp" style=""></span>°C for 10<span class="elsevierStyleHsp" style=""></span>min and immediately cooled in ice to avoid re-naturalization. The following RT mixture was prepared in 10–20<span class="elsevierStyleHsp" style=""></span>μl for each sample: 4–8<span class="elsevierStyleHsp" style=""></span>μl MMLV RT buffer (5×) (Sigma), 0.5<span class="elsevierStyleHsp" style=""></span>μl (20<span class="elsevierStyleHsp" style=""></span>U) of RNase inhibitor (RNasin, Promega) and 1<span class="elsevierStyleHsp" style=""></span>μl (100<span class="elsevierStyleHsp" style=""></span>U) of Moloney murine leukemia virus (MMLV) reverse transcriptase and incubated at 25<span class="elsevierStyleHsp" style=""></span>°C for 5<span class="elsevierStyleHsp" style=""></span>min and 37<span class="elsevierStyleHsp" style=""></span>°C for 50<span class="elsevierStyleHsp" style=""></span>min. The reaction was stopped at 95<span class="elsevierStyleHsp" style=""></span>°C for 5<span class="elsevierStyleHsp" style=""></span>min to inactivate the RT. Real-time PCR was performed using a standard TaqMan<span class="elsevierStyleSup">®</span> PCR kit protocol on a fluorescence temperature cycler, iCycler (Bio-Rad Laboratories, Hercules, CA, USA). The 20<span class="elsevierStyleHsp" style=""></span>l PCR included 0.1<span class="elsevierStyleHsp" style=""></span>ng of cDNA, 2·l TaqMan<span class="elsevierStyleSup">®</span> Universal PCR Master Mix (Applied Biosystems), 1·l of a mix of unlabelled PCR primers (COX-2 or 18S rRNA), and Taqman MGB probe (TaqMan<span class="elsevierStyleSup">®</span> Assays, Applied Biosystems, Madrid, Spain). The reactions were incubated in a 96-well plate at 95<span class="elsevierStyleHsp" style=""></span>°C for 10<span class="elsevierStyleHsp" style=""></span>min, followed by 40 cycles of 95<span class="elsevierStyleHsp" style=""></span>°C for 15 and 60<span class="elsevierStyleHsp" style=""></span>°C for 1<span class="elsevierStyleHsp" style=""></span>min. All reactions were run in triplicate. The threshold cycle (CT) is defined as the fractional cycle number at which the fluorescence passes the fixed threshold. To determine the relative expression of AR in each sample, the results were normalized to 18S (used as an internal standard) and the comparative CT method was used (User Bulletin #2 (2001), Applied Biosystem, Madrid, Spain).</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Determination of caspase 3/7 activity</span><p id="par0045" class="elsevierStylePara elsevierViewall">The cells were grown in 6-well plates at a density of 1<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>10<span class="elsevierStyleSup">5</span> cells per well and treated with the highest doses of each polyphenol used in the proliferation study. At 24 and 48<span class="elsevierStyleHsp" style=""></span>h of treatment, the media was aspirated and the cells were washed once with PBS. Then we added M-PER mammalian protein extraction reagent (Pierce, Rockford, IL, USA) with fresh protease inhibitor cocktail (Boehringer Mannheim, Germany). The cells were gently stirred for 5<span class="elsevierStyleHsp" style=""></span>min and the lysate was collected in a microfuge tube. The lysate was cleared by centrifugation at 13,000<span class="elsevierStyleHsp" style=""></span>rpm for 10<span class="elsevierStyleHsp" style=""></span>min and the supernatant was either used or immediately stored at −80<span class="elsevierStyleHsp" style=""></span>°C. The protein concentration was determined by BCA Protein Assay using the manufacturer's protocol (Pierce, Rockford, IL, USA). For apoptosis quantification we used a luminescent assay that measures caspase-3 and -7 activities (Caspase-Glo 3/7 Assay, Promega, Madison, WI, USA). Briefly, the assay provides a proluminescent substrate for caspase 3/7 in a reagent optimized for caspase activity, luciferase activity, and cell lysis. The addition of reagent results in cell lysis, caspase cleavage of the substrate, and generation of a “glow-type” luminescent signal produced by luciferase. Luminescence is proportional to the amount of caspase activity present. For this assay we used 1<span class="elsevierStyleHsp" style=""></span>μg protein for each determination.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Measurements of PGE<span class="elsevierStyleInf">2</span></span><p id="par0050" class="elsevierStylePara elsevierViewall">The cells were treated as described in the determination of caspase 3/7 activity. Levels of PGE<span class="elsevierStyleInf">2</span> released by the cells were measured by enzyme immmunoassay according to the manufacter’ instructions. Rates of produccion of PGE<span class="elsevierStyleInf">2</span> were normalized to protein concentrations (R&D Systems, Minneapolis, USA).</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Reporter plasmids and transient transfection experiments</span><p id="par0055" class="elsevierStylePara elsevierViewall">The reporter plasmids used were 5<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>NF-κB-luc (Stratagene, La Jolla, CA, USA), and luciferase-based reporter plasmid corresponding to the 5′ flanking regulatory region of human-sort COX-2 (phPESs−327/+59). These two expression vectors were transfected in PC-3 cells using Megafectin-20 (Qbiogene, Carlsbad, CA). Briefly, PC-3 cells were grown in 24-well plates at 60–80% confluence. The culture medium was then replaced by vehicle medium, that is, serum-free medium supplemented with 0.1% BSA, for 18–20<span class="elsevierStyleHsp" style=""></span>h. Then, PC-3 cells were lipotransfected with the mixture consisting of 3–4<span class="elsevierStyleHsp" style=""></span>μg of the above-mentioned plasmids incubated at room temperature for 15<span class="elsevierStyleHsp" style=""></span>min with 0.1<span class="elsevierStyleHsp" style=""></span>μl of enhancer, 3<span class="elsevierStyleHsp" style=""></span>μl of Hepes, and 2<span class="elsevierStyleHsp" style=""></span>μl of Megafectin-20 in vehicle medium. After incubation, the transfection mixture was added to cell cultures for 4<span class="elsevierStyleHsp" style=""></span>h at 37<span class="elsevierStyleHsp" style=""></span>°C in RPMI-1460 containing 5% FCS but without antibiotic liposomes. Afterwards, the transfection mixture was replaced by fresh vehicle medium containing the different compounds to be tested. At 24<span class="elsevierStyleHsp" style=""></span>h, PC-3 cells were extracted with 1_Reporter Lysis Buffer (Promega, Madison, WI, USA) for analysis of reporter gene expression. Luciferase activity was expressed as relative luciferase units/mg of protein.</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Statistical analysis</span><p id="par0060" class="elsevierStylePara elsevierViewall">Results are expressed as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>s.e.m. One-way ANOVA with Dunnett <span class="elsevierStyleItalic">t</span>-test <span class="elsevierStyleItalic">post hoc</span> analysis was used to compare ARM expression analysis between treated and control groups. Comparisons with regard to caspase 3/7 activity were carried out with Student’ unpaired <span class="elsevierStyleItalic">t</span>-test. Significance level was reached when <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05.</p></span></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Results</span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Polyphenols suppress PMA-mediated increase in the production of PGE<span class="elsevierStyleInf">2</span></span><p id="par0065" class="elsevierStylePara elsevierViewall">In these experiments, four polyphenols were tested with regard to their effect on the production on PGE<span class="elsevierStyleInf">2</span> to determine the anti-inflammatory effects of these polyphenols: the stilbene resveratrol, the flavonol quercetin, the tannin tannic acid, and the benzoic acid and gallic acid (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). Phorbol esters are potent inducers of COX-2, so we determined the effect of tannic, gallic acid, quercetin, and resveratrol on the synthesis of PGs by PC-3 cells in which COX-2 was induced by PMA. As shown in <a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>A, PMA caused about a 4-fold increase in the synthesis of PGE<span class="elsevierStyleInf">2</span>. This effect was markedly supressed by treatment with resveratrol (82%), tannic acid (64%), and quercetin (41%); and it was lightness inhibited by gallic acid (17%). To evaluate whether the inhibition of PGE<span class="elsevierStyleInf">2</span> synthesis was because of inhibition of COX-2 or COX-1, we compared the effects of NS-398, a selective inhibitor of COX-2. Pretreatment of cells with NS-398 (0.1–10<span class="elsevierStyleHsp" style=""></span>M) inhibited the synthesis of PGs to less than 10% of the PMA-stimulated control level (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>B). This result means that more than 90% of the PMA-stimulated COX activity in PC-3 cells was because of the COX-2 isoform. We did not find any change in the levels of PGE<span class="elsevierStyleInf">2</span> synthesis in absence of PMA (data not shown).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Polyphenols inhibit PMA-mediated increase in COX-2 mRNA</span><p id="par0070" class="elsevierStylePara elsevierViewall">To determine whether the above effects on production of PGE<span class="elsevierStyleInf">2</span> could be related to differences in levels of mRNA COX-2, real-time RT-PCR of total RNA was carried out. <a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a> shows that treatment with PMA resulted in a marked increase (3-fold) in levels of COX-2 mRNA expression <span class="elsevierStyleItalic">versus</span> no treated cells (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>0.01). This effect was partially suppressed by polyphenols. Resveratrol and quercetin inhibited COX-2 expression 63% and 47%, respectively. However, tannic and gallic acids inhibited COX-2 mRNA expression to a lesser extent (20–25%). These data indicated that these polyphenols inhibited COX-2 expression at the transcription levels, resveratrol and quercetin being the most potent inhibitors. We did not find any change in the levels of COX-2 mRNA in absence of PMA (data not shown).</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Effect of polyphenols on NF-κB and Cox-2 activity</span><p id="par0075" class="elsevierStylePara elsevierViewall">To further investigate the importance of PMA and polyphenols in modulating the expression of COX-2, transient transfections were performed using a reporter plasmid bearing the short (−327/+59pb) human COX-2 promoter. As in mRNA, the treatment with PMA for 24<span class="elsevierStyleHsp" style=""></span>h significantly increased activity of the luciferase-based promoter construct about >7-fold. All polyphenols caused inhibition of PMA-mediated induction of COX-2 promoter activity (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>).</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0080" class="elsevierStylePara elsevierViewall">Because activation of NF-κB is critical for induction of COX-2 by phorbol esters, we also studied whether one of the main transcription factors involved in the inflammatory response, NF-κB, is inhibited in the signal transducction pathway leading to COX-2 expression caused by PMA. For this purpose, we determined NF-κB-dependent transcription basal activity in PC-3 transiently transfected with p5<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>NF-κB-luc. Stimulation of cells with PMA for 24<span class="elsevierStyleHsp" style=""></span>h results in a 2-fold increased NF-κB luciferase activity. This stimulation was partially suppressed by gallic (24%), tannic acid (33%), and quercetin (37%) (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>). Resveratrol was the most potent, and it was capable of inhibiting almost totally (>90%) the activity of NF-κB promoter even with respect to basal conditions, in the absence of PMA (>90% inhibition).</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Induction of apoptosis by polyphenols on PC-3 cells</span><p id="par0085" class="elsevierStylePara elsevierViewall">Caspase 3/7 activity in control and polyphenols treated cells was determined to assess whether the inhibition of COX-2 metabolism (PGE2 expression and secretion) may cause induction of apoptosis. PC-3 cells were treated for 24 and 48<span class="elsevierStyleHsp" style=""></span>h in presence of different polyphenols (10<span class="elsevierStyleHsp" style=""></span>M), lysed and measured for the presence of active caspase 3/7 with Caspase-Glo 3/7 Assay. Caspase 3/7 activity was significantlly increased by all polyphenols tested with respect to control at 48<span class="elsevierStyleHsp" style=""></span>h, although at a different rate: quercetin 1.6, gallic acid 1.7, tannic acid 3.5, and resveratrol 42.5 times compared to control (<a class="elsevierStyleCrossRef" href="#fig0030">Fig. 6</a>A). Minor differences can be better perceived in detail (<a class="elsevierStyleCrossRef" href="#fig0030">Fig. 6</a>B).</p><elsevierMultimedia ident="fig0030"></elsevierMultimedia></span></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Discussion</span><p id="par0090" class="elsevierStylePara elsevierViewall">Resveratrol is a phytoalexin found in high concentrations in grapes and has been shown to inhibit chemical carcinogens in several models.<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> This natural compound has been proposed of therapeutic potential in preclinical, animal models, and human studies in several malignancies.<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> Specific interest has emerged in prostate cancer, since resveratrol has proved AR expression transcriptional regression, accelerated AR degradation, and modulation of AR co-activators.<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">16,19–21</span></a> Resveratrol in the diet spontaneously suppresses developing prostate tumors in the Transgenic Adenocarcinoma Mouse Prostate (TRAMP) model through down-regulation of phospho-ERK, a downstream effector of sex steroid receptor and growth factor signaling.<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">22</span></a> High concentrations of resveratrol have also resulted in dose-dependent significant inhibition of PKB/Akt phosphorylation, both in PC-3 and LNCaP cell lines.<a class="elsevierStyleCrossRefs" href="#bib0115"><span class="elsevierStyleSup">23,24</span></a> Resveratrol-mediated PI3Kinhibition may be mediated in part by inhibition of FOXO family tumor suppression phosphorylation, thus allowing for proapototic targets like TRAIL or p27.<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a></p><p id="par0095" class="elsevierStylePara elsevierViewall">In mammary adenocarcinoma, resveratrol has been proved to inhibit the enzyme COX-2, inducible isoform of the rate-limiting enzymes that convert arachidonic acid to proinflammatory prostaglandins, which is increased following stimulation of mitogens, such as phorbol ester.<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">18,26</span></a> This inhibition was manifested at different levels, which include direct enzymatic activity, mRNA and protein synthesis, cyclic AMP response element, and AP-1 mediated gene expression.<a class="elsevierStyleCrossRefs" href="#bib0130"><span class="elsevierStyleSup">26,27</span></a> Resveratrol has also been confirmed to suppress COX-2 promoter activity in DLD-1 human colonic cancer cells.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> Regarding the prostate, COX-2 is up-regulated in proliferative inflammatory atrophy (PIA) of the prostate, but not in PCa,<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> although it has been advocated to promote prostate cancer progression.<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> Catechins present in green tea inhibit COX-2 without affecting COX-1 expression at mRNA and protein levels, both in androgen-responsive LNCaP and androgen-refractory PC-3. This action has been proven both <span class="elsevierStyleItalic">in vitro</span> and <span class="elsevierStyleItalic">in vivo</span> using the TRAMP mouse model.<a class="elsevierStyleCrossRefs" href="#bib0155"><span class="elsevierStyleSup">31,32</span></a> Also the effects of green tea polyphenols on PCa are synergistic with COX-2 inhibitors.<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">The COX-2 inflammatory pathway is considered a potential target in epithelial neoplasm, and also specifically in PCa. The activation of NF-κB is considered critical for induction of COX-2 by phorbol esters.<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a> What is more, overexpressed COX-2 is secondary to overexpression of NF-κβ.<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> Hussain et al. demonstrated that the constituent of green tea epigallocatechin-3-gallate selectively inhibits COX-2 in human prostate carcinoma cells, both LNCaP and PC-3.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> This action is the same we demonstrate is exerted by resveratrol and other polyphenols in red wine, all abundant in the Mediterranean diet.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a></p><p id="par0105" class="elsevierStylePara elsevierViewall">NF-κβ is a transcription factor often overexpressed that regulates different cellular activities including inflammation, immunity, and cell death. Downregulation of NF-κβ is known to trigger apoptotic and antiproliferative effects and is considered a likely mechanism to render health benefits of green tea polyphenols intake.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> However, reality is very complex because green tea polyphenols target many other different mechanisms, including cell-cycle arrest, detoxification enzymes, IGF, TRAIL-induced apoptosis, MAP kinases, Hh (Hedgehog signaling) PI3K-Akt (rapamycin signaling), and PKC.<a class="elsevierStyleCrossRefs" href="#bib0195"><span class="elsevierStyleSup">39,40</span></a> According to our results, polyphenols in red wine also target the inflammatory pathways and could be responsible for the <span class="elsevierStyleItalic">in vitro</span> antiproliferative effect of resveratrol, quercetin, gallic acid, and tannic acid on PC-3 cell line. This signaling appears totally different from that of the AR observed in LNCaP cell line.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> Inhibition of NF-κβ signaling in TRAMP mice activates apoptosis trough increased Bax/Bcl-2 ratio.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> This effect has also been demonstrated for pomegranate juice of the <span class="elsevierStyleItalic">Punica granatum</span> fruit<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a>; delphinidin, a major anthocyanid present in many pigmented fruits and vegetables,<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">43</span></a> and also recently α-tomatine, the major saponin present in tomato (<span class="elsevierStyleItalic">Lycopersicon esculentum</span>).<a class="elsevierStyleCrossRefs" href="#bib0220"><span class="elsevierStyleSup">44,45</span></a> It is very understandable that the mechanism we describe for resveratrol and other red wine polyphenols on androgen-refractory PC-3 cell line of prostate cancer follows a very similar rationale.</p><p id="par0110" class="elsevierStylePara elsevierViewall">In this study, we show that different polyphenols present in red wine inhibit PMA stimulation of COX-2 expression, promoter activity for COX-2, and PGE<span class="elsevierStyleInf">2</span> release in androgen-insensitive PC-3 human prostate carcinoma leading to increased apoptosis. Despite the large accumulated experience <span class="elsevierStyleItalic">in vitro</span> very few clinical trials using precise concentrations of likely chemopreventive compounds have been conducted. In this sense, a randomized phase II study has recently shown that pomegranate extract is associated with more than 6-month increase in PSA doubling time in men with biochemical recurrence after local therapy; however, no control arm was used.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a></p><p id="par0115" class="elsevierStylePara elsevierViewall">Definitely there is no evidence to consider resveratrol a therapeutic antineoplasic agent. However, it has been considered to enhance radiation sensitivity in several malignancies, including prostate.<a class="elsevierStyleCrossRefs" href="#bib0235"><span class="elsevierStyleSup">47,48</span></a> Possibly in the future some beneficial role might be found as adjunct in the management of castrate-resistant disease, or at least be beneficial to attenuate PCa progression. At present, we must admit that, from the clinical perspective, the effect of dietary antioxidants on prostate cancer remains undefined.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a></p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Conflict of interest</span><p id="par0120" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflict of interest.</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Funding</span><p id="par0125" class="elsevierStylePara elsevierViewall">This work has been funded by the grant <span class="elsevierStyleGrantSponsor" id="gs1">Foundation for Research in Urology</span> (FIU) of the Spanish Association of Urology.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:11 [ 0 => array:2 [ "identificador" => "xres364427" "titulo" => array:5 [ 0 => "Abstract" 1 => "Objective" 2 => "Material and method" 3 => "Results" 4 => "Conclusions" ] ] 1 => array:2 [ "identificador" => "xpalclavsec344031" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres364428" "titulo" => array:5 [ 0 => "Resumen" 1 => "Objetivo" 2 => "Material y método" 3 => "Resultados" 4 => "Conclusiones" ] ] 3 => array:2 [ "identificador" => "xpalclavsec344032" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:3 [ "identificador" => "sec0010" "titulo" => "Materials and methods" "secciones" => array:7 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Materials" ] 1 => array:2 [ "identificador" => "sec0020" "titulo" => "Cell culture and treatments" ] 2 => array:2 [ "identificador" => "sec0025" "titulo" => "RNA extraction and real-time PCR for COX-2 expressions" ] 3 => array:2 [ "identificador" => "sec0030" "titulo" => "Determination of caspase 3/7 activity" ] 4 => array:2 [ "identificador" => "sec0035" "titulo" => "Measurements of PGE" ] 5 => array:2 [ "identificador" => "sec0040" "titulo" => "Reporter plasmids and transient transfection experiments" ] 6 => array:2 [ "identificador" => "sec0045" "titulo" => "Statistical analysis" ] ] ] 6 => array:3 [ "identificador" => "sec0050" "titulo" => "Results" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "sec0055" "titulo" => "Polyphenols suppress PMA-mediated increase in the production of PGE" ] 1 => array:2 [ "identificador" => "sec0060" "titulo" => "Polyphenols inhibit PMA-mediated increase in COX-2 mRNA" ] 2 => array:2 [ "identificador" => "sec0065" "titulo" => "Effect of polyphenols on NF-κB and Cox-2 activity" ] 3 => array:2 [ "identificador" => "sec0070" "titulo" => "Induction of apoptosis by polyphenols on PC-3 cells" ] ] ] 7 => array:2 [ "identificador" => "sec0075" "titulo" => "Discussion" ] 8 => array:2 [ "identificador" => "sec0080" "titulo" => "Conflict of interest" ] 9 => array:2 [ "identificador" => "sec0085" "titulo" => "Funding" ] 10 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2014-02-19" "fechaAceptado" => "2014-02-24" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec344031" "palabras" => array:6 [ 0 => "Castrate-resistant prostate cancer" 1 => "PC-3 cell line" 2 => "Resveratrol" 3 => "Polyphenols" 4 => "COX-2" 5 => "NF-κβ" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec344032" "palabras" => array:6 [ 0 => "Cáncer de próstata resistente a castración" 1 => "Línea celular PC-3" 2 => "Resveratrol" 3 => "Polifenoles" 4 => "COX-2" 5 => "NF-κβ" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span class="elsevierStyleSectionTitle" id="sect0010">Objective</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Mediterranean diet may play a role in the prevention of prostate cancer (PCa) development and progression. Cyclooxygenase-2 (COX-2) expression is associated with increased cellular proliferation, prevents apoptosis and favors tumor invasion. We intend to clarify whether resveratrol and other polyphenols effectively inhibit COX-2 activity and induce apoptosis in hormone-resistant PC-3 cell line.</p> <span class="elsevierStyleSectionTitle" id="sect0015">Material and method</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">PC-3 cells were cultured and treated with different concentrations of gallic acid, tannic acid, quercetin, and resveratrol in presence of phorbol myristate acetate (PMA; 50<span class="elsevierStyleHsp" style=""></span>μg/ml) that induces COX-2 expression. Total RNA was extracted and COX-2 expression was analyzed by relative quantification real-time PCR (ΔΔCt method). COX-2 activity was determined by PGE-2 detection using ELISA. Caspase 3/7 luminescence assay was used to disclose apoptosis. Transitory transfection with short human COX-2 (phPES2 −327/+59) and p5xNF-κβ-Luc plasmids determined COX-2 promoter activity and specifically that dependant of NF-κβ.</p> <span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">COX-2 expression was not modified in media devoid of PMA. However, under PMA induction tannic acid (2.08<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.21), gallic acid (2.46<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.16), quercetin (1.78<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.14) and resveratrol (1.15<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.16) significantly inhibited COX-2 mRNA with respect to control (3.14<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.07), what means a 34%, 23%, 46% and 61% reduction, respectively. The inhibition in the levels of PGE-2 followed a similar pattern. All compounds studied induced apoptosis at 48<span class="elsevierStyleHsp" style=""></span>h, although at a different rate. PMA caused a rise in activity 7.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.23 times phPES2 −327/+59 and 2.0<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.1 times p5<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>NF-κβ-Luc at 6<span class="elsevierStyleHsp" style=""></span>h compared to basal. Resveratrol suppressed these effects 17.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.21 and 32.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>.18 times, respectively. Similarly, but to a lesser extent, the rest of evaluated polyphenols diminished PMA inductor effect on the activity of both promoters.</p> <span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Polyphenols inhibit transcriptional activity of COX-2 promoter mediated by NF-κβ. This effect could explain, at least in part, the induction of apoptosis <span class="elsevierStyleItalic">in vitro</span> by these substances in castration resistant PCa.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<span class="elsevierStyleSectionTitle" id="sect0035">Objetivo</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">La dieta mediterránea puede tener un papel en la prevención del desarrollo y progresión del cáncer de próstata (CaP). La expresión de ciclooxigenasa-2 (COX-2) se asocia con la proliferación celular aumentada, previene la apoptosis y favorece la invasión tumoral. Se intenta clarificar si el resveratrol y otros polifenoles del vino inhiben de forma efectiva la actividad de COX-2 e inducen apoptosis en la línea celular PC-3 de cáncer hormonorrefractario.</p> <span class="elsevierStyleSectionTitle" id="sect0040">Material y método</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Células PC-3 fueron cultivadas y tratadas con diferentes concentraciones de ácido gálico, ácido tánico, quercetina y resveratrol en presencia del éster de forbol PMA (50<span class="elsevierStyleHsp" style=""></span>μg/ml) que induce la expresión de COX-2. Se extrajo ARN total y se analizó la expresión de COX-2 mediante cuantificación relativa por PCR a tiempo real (método ΔΔCt). La actividad COX-2 se determinó mediante detección de PGE-2 por la técnica ELISA. Se empleó ensayo de luminiscencia caspasa-3/7 para evaluar la apoptosis. La transfección transitoria con plásmidos <span class="elsevierStyleItalic">short human</span> COX-2 (phPES2 −327/+59) y p5xNF-κβ-Luc determinó la actividad del promotor de COX-2, y de forma particular, la dependiente de NF-κβ.</p> <span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">La expresión de COX-2 no se modificó en ausencia de PMA. No obstante, bajo la inducción con PMA, ácido tánico (2,08<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,21), ácido gálico (2,46<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,16), quercetina (1,78<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,14) y, especialmente resveratrol (1,15<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,16) inhibieron significativamente la expresión de COX-2 respecto al control (3,14<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,07), causando una reducción del 34, 23, 46 y 61%, respectivamente. La inhibición en los niveles de PGE-2 siguió un patrón similar. Todos los compuestos estudiados indujeron apoptosis a las 48<span class="elsevierStyleHsp" style=""></span>h, aunque en diferente proporción. El PMA causó un aumento de la actividad de 7,4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,23 veces phPES2 −327/+59 y 2,0<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,1 veces p5<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>NF-κβ-Luc a 6<span class="elsevierStyleHsp" style=""></span>h sobre los niveles basales. El resveratrol suprimió estos efectos 17,1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,21 y 32,4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0,18 veces, respectivamente. De forma similar, aunque en menor medida, el resto de polifenoles evaluados disminuyeron el efecto inductor de PMA sobre la actividad de ambos promotores.</p> <span class="elsevierStyleSectionTitle" id="sect0050">Conclusiones</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Los polifenoles inhiben la actividad transcripcional del promotor de COX-2 mediada por NF-κβ. Este efecto podría explicar, al menos en parte, la inducción <span class="elsevierStyleItalic">in vitro</span> de apoptosis por estas sustancias en el CaP resistente a la castración.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Ferruelo A, de las Heras MM, Redondo C, Ramón de Fata F, Romero I, Angulo JC. Los polifenoles del vino ejercen su efecto antineoplásico sobre la línea celular PC-3 andrógeno resistente a través de la inhibición de la actividad transcripcional del promotor de COX-2 mediada por NF-κβ. Actas Urol Esp. 2014;38:429–437.</p>" ] ] "multimedia" => array:6 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 3831 "Ancho" => 2937 "Tamanyo" => 233789 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Biochemical structure of the different polyphenols studied (resveratrol, quercetin, tannic acid and gallic acid) and chemical groups they correspond to.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 2406 "Ancho" => 1624 "Tamanyo" => 113962 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Polyphenols suppress phorbol ester-mediated elevated in the production of PGE<span class="elsevierStyleInf">2</span>. PC-3 cells were treated with or without PMA (50<span class="elsevierStyleHsp" style=""></span>μg/ml) and 10<span class="elsevierStyleHsp" style=""></span>μM of gallic and tannic acid, quercetin, resveratrol and vehicle (0.01% ethanol) (A) or NS398 (0–10<span class="elsevierStyleHsp" style=""></span>μM) (B) for 48<span class="elsevierStyleHsp" style=""></span>h. The medium was collected to determine the rate of synthesis of PGE<span class="elsevierStyleInf">2</span>. Production of PGE<span class="elsevierStyleInf">2</span> was determined by enzyme immunoassay. <span class="elsevierStyleSup">*</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; <span class="elsevierStyleSup">**</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.01 <span class="elsevierStyleItalic">vs.</span> PMA treatment.</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 1207 "Ancho" => 1648 "Tamanyo" => 71977 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Effect of polyphenols on PMA-induced COX-2 mRNA levels in PC-3 cells treated with or without PMA (50<span class="elsevierStyleHsp" style=""></span>μg/ml) and 10<span class="elsevierStyleHsp" style=""></span>μM of gallic and tannic acid, quercetin, resveratrol or vehicle (0.01% ethanol) for 24<span class="elsevierStyleHsp" style=""></span>h. Total cellular RNA was isolated and analyzed by real-time RT-PCR for COX-2 expression. The 18S rRNA gene was amplified as an internal control. A significant decrease in COX-2 mRNA expression was observed for all polyphenols. Resveratrol was the most potent. <span class="elsevierStyleSup">*</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; <span class="elsevierStyleSup">**</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.01 <span class="elsevierStyleItalic">vs.</span> PMA treatment.</p>" ] ] 3 => array:7 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 1116 "Ancho" => 1615 "Tamanyo" => 56759 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Effect of polyphenols on PMA-induced COX-2 promoter activity. PC-3 cells were transiently transfected with 3–4<span class="elsevierStyleHsp" style=""></span>μg of plasmid phCOX-2 (−327/+59)-luc. After transfection, cells were treated with vehicle (white column), PMA (50<span class="elsevierStyleHsp" style=""></span>μg/ml, black column), or PMA and polyphenols (10<span class="elsevierStyleHsp" style=""></span>μM, rest of columns). Reporter activity was measured in cellular extracts 24<span class="elsevierStyleHsp" style=""></span>h later. Luciferase activity represents data that have been normalized with protein concentration. <span class="elsevierStyleSup">*</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; <span class="elsevierStyleSup">**</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.01 <span class="elsevierStyleItalic">versus</span> PMA treatment.</p>" ] ] 4 => array:7 [ "identificador" => "fig0025" "etiqueta" => "Figure 5" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr5.jpeg" "Alto" => 1193 "Ancho" => 1657 "Tamanyo" => 68569 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Effect of polyphenols on PMA-induced NF-κB promoter activity. PC-3 cells were transiently transfected with 3–4<span class="elsevierStyleHsp" style=""></span>μg of plasmid phCOX-2 (−327/+59)-luc. After transfection, cells were treated with vehicle (white column), PMA (50<span class="elsevierStyleHsp" style=""></span>μg/ml, black column), or PMA and polyphenols (10<span class="elsevierStyleHsp" style=""></span>μM, rest of columns). Reporter activity was measured in cellular extracts 24<span class="elsevierStyleHsp" style=""></span>h later. Luciferase activity represents data that have been normalized with protein concentration. <span class="elsevierStyleSup">*</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; <span class="elsevierStyleSup">**</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.01 <span class="elsevierStyleItalic">versus</span> PMA treatment.</p>" ] ] 5 => array:7 [ "identificador" => "fig0030" "etiqueta" => "Figure 6" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr6.jpeg" "Alto" => 2149 "Ancho" => 1638 "Tamanyo" => 91843 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Induction of apoptosis by polyphenols on PC-3 cells determined by caspase 3/7 activity in control and treated cells. All compounds induced apoptosis at 48<span class="elsevierStyleHsp" style=""></span>h, although at a different rate: tannic acid 3.5, gallic acid 1.7, quercetin 1.6 and resveratrol 42.5 times compared to control (A). Minor differences can be appreciated in detail (B).</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:49 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Nutrition and cancer: a review of the evidence for anti-cancer diet" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:1 [ 0 => "M.S. 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