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A role of androgen receptor protein in cell growth of an androgen-independent prostate cancer cell line
Prostate cancer, which develops due to androgen and is initially responsive to androgen deprivation therapy, often comes to acquire androgen deprivation therapy resistance in short order. We investigated the role of androgen receptor (AR) protein in an androgen-independent prostate cancer cell line...
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Published in: | Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2005-11, Vol.69 (11), p.2236-2239 |
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container_end_page | 2239 |
container_issue | 11 |
container_start_page | 2236 |
container_title | Bioscience, biotechnology, and biochemistry |
container_volume | 69 |
creator | Furutani, T.(Astellas Pharma Inc., Tsukuba, Ibaraki (Japan). Drug Discovery Research) Takeyama, K Koutoku, H Ito, S Taniguchi, N Suzuki, E Kudoh, M Shibasaki, M Shikama, H Kato, S |
description | Prostate cancer, which develops due to androgen and is initially responsive to androgen deprivation therapy, often comes to acquire androgen deprivation therapy resistance in short order. We investigated the role of androgen receptor (AR) protein in an androgen-independent prostate cancer cell line using AR ligands and AR siRNA. Although the androgen-independent cell line scarcely responded to AR ligands, their growth was attenuated by ablation of AR protein by siRNA. |
doi_str_mv | 10.1271/bbb.69.2236 |
format | article |
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Drug Discovery Research) ; Takeyama, K ; Koutoku, H ; Ito, S ; Taniguchi, N ; Suzuki, E ; Kudoh, M ; Shibasaki, M ; Shikama, H ; Kato, S</creator><creatorcontrib>Furutani, T.(Astellas Pharma Inc., Tsukuba, Ibaraki (Japan). Drug Discovery Research) ; Takeyama, K ; Koutoku, H ; Ito, S ; Taniguchi, N ; Suzuki, E ; Kudoh, M ; Shibasaki, M ; Shikama, H ; Kato, S</creatorcontrib><description>Prostate cancer, which develops due to androgen and is initially responsive to androgen deprivation therapy, often comes to acquire androgen deprivation therapy resistance in short order. We investigated the role of androgen receptor (AR) protein in an androgen-independent prostate cancer cell line using AR ligands and AR siRNA. Although the androgen-independent cell line scarcely responded to AR ligands, their growth was attenuated by ablation of AR protein by siRNA.</description><identifier>ISSN: 0916-8451</identifier><identifier>EISSN: 1347-6947</identifier><identifier>DOI: 10.1271/bbb.69.2236</identifier><identifier>PMID: 16306710</identifier><language>eng</language><publisher>Tokyo: Japan Society for Bioscience, Biotechnology, and Agrochemistry</publisher><subject>androgen receptor ; androgen receptor antagonist ; ANDROGENE ; ANDROGENOS ; ANDROGENS ; Androgens - pharmacology ; Biological and medical sciences ; Cell Line, Tumor ; Cell Proliferation - drug effects ; CELLS ; CELLULE ; CELULAS ; CRECIMIENTO ; CROISSANCE ; ESTEROIDES ; EXPRESION GENICA ; EXPRESSION DES GENES ; Fundamental and applied biological sciences. Psychology ; GENE EXPRESSION ; GROWTH ; HORMONE RECEPTORS ; Humans ; IMMUNOBLOTTING ; Ligands ; Male ; NEOPLASMAS ; NEOPLASME ; NEOPLASMS ; PROSTATA ; PROSTATE ; prostate cancer ; Prostatic Neoplasms - pathology ; RECEPTEUR D'HORMONE ; RECEPTORES DE HORMONAS ; Receptors, Androgen - genetics ; Receptors, Androgen - physiology ; RNA, Small Interfering - pharmacology ; STEROIDE ; STEROIDS</subject><ispartof>Bioscience, biotechnology, and biochemistry, 2005-11, Vol.69 (11), p.2236-2239</ispartof><rights>2005 by Japan Society for Bioscience, Biotechnology, and Agrochemistry 2005</rights><rights>2006 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c667t-c6422eb7de33b73f39adb824ee003cc197511aca17c10246cf474c1bfe7a96b73</citedby><cites>FETCH-LOGICAL-c667t-c6422eb7de33b73f39adb824ee003cc197511aca17c10246cf474c1bfe7a96b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17485573$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16306710$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Furutani, T.(Astellas Pharma Inc., Tsukuba, Ibaraki (Japan). Drug Discovery Research)</creatorcontrib><creatorcontrib>Takeyama, K</creatorcontrib><creatorcontrib>Koutoku, H</creatorcontrib><creatorcontrib>Ito, S</creatorcontrib><creatorcontrib>Taniguchi, N</creatorcontrib><creatorcontrib>Suzuki, E</creatorcontrib><creatorcontrib>Kudoh, M</creatorcontrib><creatorcontrib>Shibasaki, M</creatorcontrib><creatorcontrib>Shikama, H</creatorcontrib><creatorcontrib>Kato, S</creatorcontrib><title>A role of androgen receptor protein in cell growth of an androgen-independent prostate cancer cell line</title><title>Bioscience, biotechnology, and biochemistry</title><addtitle>Biosci Biotechnol Biochem</addtitle><description>Prostate cancer, which develops due to androgen and is initially responsive to androgen deprivation therapy, often comes to acquire androgen deprivation therapy resistance in short order. We investigated the role of androgen receptor (AR) protein in an androgen-independent prostate cancer cell line using AR ligands and AR siRNA. Although the androgen-independent cell line scarcely responded to AR ligands, their growth was attenuated by ablation of AR protein by siRNA.</description><subject>androgen receptor</subject><subject>androgen receptor antagonist</subject><subject>ANDROGENE</subject><subject>ANDROGENOS</subject><subject>ANDROGENS</subject><subject>Androgens - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>CELLS</subject><subject>CELLULE</subject><subject>CELULAS</subject><subject>CRECIMIENTO</subject><subject>CROISSANCE</subject><subject>ESTEROIDES</subject><subject>EXPRESION GENICA</subject><subject>EXPRESSION DES GENES</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GENE EXPRESSION</subject><subject>GROWTH</subject><subject>HORMONE RECEPTORS</subject><subject>Humans</subject><subject>IMMUNOBLOTTING</subject><subject>Ligands</subject><subject>Male</subject><subject>NEOPLASMAS</subject><subject>NEOPLASME</subject><subject>NEOPLASMS</subject><subject>PROSTATA</subject><subject>PROSTATE</subject><subject>prostate cancer</subject><subject>Prostatic Neoplasms - pathology</subject><subject>RECEPTEUR D'HORMONE</subject><subject>RECEPTORES DE HORMONAS</subject><subject>Receptors, Androgen - genetics</subject><subject>Receptors, Androgen - physiology</subject><subject>RNA, Small Interfering - pharmacology</subject><subject>STEROIDE</subject><subject>STEROIDS</subject><issn>0916-8451</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNptkMFrFDEUh4Mo7bb25NkyIHqRWfOSTDJzLMVapdAe9BwymZd1ymyyJllK_3szzGqhFMILhO_3-OUj5B3QNTAFX_q-X8tuzRiXr8gKuFC17IR6TVa0A1m3ooFjcpLSPaXloYEjcgySU6mArsjmoophwiq4yvghhg36KqLFXQ6x2sWQcfRVORanqdrE8JB_L-x_vB79gDssw-c5kbLJWFnjLcYlNo0e35I3zkwJzw73Kfl19fXn5XV9c_vt--XFTW2lVLlMwRj2akDOe8Ud78zQt0wgUsqthU41AMYaUBYoE9I6oYSF3qEynSyJU_Jp2Vua_Nljyno7prmF8Rj2Scu2bBPtDH54Bt6HffSlmwYhuhaopKxQnxfKlo-liE7v4rg18VED1bN9Xexr2enZfqHPDzv3_RaHJ_aguwAfD4BJ1kwuFktjeuKUaJtG8cLJhRu9C3FrHkKcBp3N4xTivxB_ucH7JehM0GYTC_fjjlGqij7eMv4XsfSoIw</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Furutani, T.(Astellas Pharma Inc., Tsukuba, Ibaraki (Japan). 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Drug Discovery Research) ; Takeyama, K ; Koutoku, H ; Ito, S ; Taniguchi, N ; Suzuki, E ; Kudoh, M ; Shibasaki, M ; Shikama, H ; Kato, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c667t-c6422eb7de33b73f39adb824ee003cc197511aca17c10246cf474c1bfe7a96b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>androgen receptor</topic><topic>androgen receptor antagonist</topic><topic>ANDROGENE</topic><topic>ANDROGENOS</topic><topic>ANDROGENS</topic><topic>Androgens - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>CELLS</topic><topic>CELLULE</topic><topic>CELULAS</topic><topic>CRECIMIENTO</topic><topic>CROISSANCE</topic><topic>ESTEROIDES</topic><topic>EXPRESION GENICA</topic><topic>EXPRESSION DES GENES</topic><topic>Fundamental and applied biological sciences. 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source | Free E-Journal (出版社公開部分のみ); Oxford Journals Online |
subjects | androgen receptor androgen receptor antagonist ANDROGENE ANDROGENOS ANDROGENS Androgens - pharmacology Biological and medical sciences Cell Line, Tumor Cell Proliferation - drug effects CELLS CELLULE CELULAS CRECIMIENTO CROISSANCE ESTEROIDES EXPRESION GENICA EXPRESSION DES GENES Fundamental and applied biological sciences. Psychology GENE EXPRESSION GROWTH HORMONE RECEPTORS Humans IMMUNOBLOTTING Ligands Male NEOPLASMAS NEOPLASME NEOPLASMS PROSTATA PROSTATE prostate cancer Prostatic Neoplasms - pathology RECEPTEUR D'HORMONE RECEPTORES DE HORMONAS Receptors, Androgen - genetics Receptors, Androgen - physiology RNA, Small Interfering - pharmacology STEROIDE STEROIDS |
title | A role of androgen receptor protein in cell growth of an androgen-independent prostate cancer cell line |
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