Differential androgen modulation of AXC/SSh rat prostate cancer cell proliferation in Vitro and its antagonism by antiandrogen

We examined androgen modulation of proliferation of clonally derived AXC/SSh rat prostate cancer cells. C-family cells were maintained on medium without addition of androgens. D-family cells were maintained on medium containing 10(-7) M 5 alpha-dihydrotestosterone and T-family cells were maintained...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 1986-08, Vol.46 (8), p.3775-3781
Hauptverfasser: HUOT, R. I, SHAIN, S. A
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SHAIN, S. A
description We examined androgen modulation of proliferation of clonally derived AXC/SSh rat prostate cancer cells. C-family cells were maintained on medium without addition of androgens. D-family cells were maintained on medium containing 10(-7) M 5 alpha-dihydrotestosterone and T-family cells were maintained on medium containing 10(-7) M testosterone. Proliferation of all AXC/SSh prostate cancer cell lines during propagation on media containing fetal bovine serum was not altered by changes in media testosterone concentration through the range 10(-6) to 10(-9) M. Similarly, proliferation of C- or D-family cell lines, during propagation on media containing steroid depleted, charcoal stripped fetal bovine serum, was not altered by changes in media testosterone concentration through the range 10(-6) to 10(-9) M. By contrast, proliferation of T-family cell lines during propagation on charcoal stripped fetal bovine serum was modulated by androgens; effects were androgen concentration dependent and maximum at 10(-8) to 10(-7) M. Androgens decreased T5 cell proliferation rate and diminished achievable saturation density, whereas T1 cell proliferation rate was increased by androgens. In contrast, T6 cell proliferation rate was unaffected by androgens; however, saturation density was increased. Effects were antagonized by the antiandrogen RU 23908, Anandron, establishing androgen specificity of testosterone or 5 alpha-dihydrotestosterone mediated changes in proliferation.
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By contrast, proliferation of T-family cell lines during propagation on charcoal stripped fetal bovine serum was modulated by androgens; effects were androgen concentration dependent and maximum at 10(-8) to 10(-7) M. Androgens decreased T5 cell proliferation rate and diminished achievable saturation density, whereas T1 cell proliferation rate was increased by androgens. In contrast, T6 cell proliferation rate was unaffected by androgens; however, saturation density was increased. 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I</creatorcontrib><creatorcontrib>SHAIN, S. A</creatorcontrib><title>Differential androgen modulation of AXC/SSh rat prostate cancer cell proliferation in Vitro and its antagonism by antiandrogen</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>We examined androgen modulation of proliferation of clonally derived AXC/SSh rat prostate cancer cells. C-family cells were maintained on medium without addition of androgens. D-family cells were maintained on medium containing 10(-7) M 5 alpha-dihydrotestosterone and T-family cells were maintained on medium containing 10(-7) M testosterone. Proliferation of all AXC/SSh prostate cancer cell lines during propagation on media containing fetal bovine serum was not altered by changes in media testosterone concentration through the range 10(-6) to 10(-9) M. Similarly, proliferation of C- or D-family cell lines, during propagation on media containing steroid depleted, charcoal stripped fetal bovine serum, was not altered by changes in media testosterone concentration through the range 10(-6) to 10(-9) M. By contrast, proliferation of T-family cell lines during propagation on charcoal stripped fetal bovine serum was modulated by androgens; effects were androgen concentration dependent and maximum at 10(-8) to 10(-7) M. Androgens decreased T5 cell proliferation rate and diminished achievable saturation density, whereas T1 cell proliferation rate was increased by androgens. In contrast, T6 cell proliferation rate was unaffected by androgens; however, saturation density was increased. 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Experimental tumors</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Division - drug effects</topic><topic>Cell Line</topic><topic>Dehydroepiandrosterone - analogs &amp; derivatives</topic><topic>Dehydroepiandrosterone - pharmacology</topic><topic>Dehydroepiandrosterone Sulfate</topic><topic>Experimental renal and urinary tract tumors</topic><topic>Imidazoles - pharmacology</topic><topic>Imidazolidines</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Rats</topic><topic>Receptors, Androgen - analysis</topic><topic>Testosterone - pharmacology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HUOT, R. I</creatorcontrib><creatorcontrib>SHAIN, S. 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A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential androgen modulation of AXC/SSh rat prostate cancer cell proliferation in Vitro and its antagonism by antiandrogen</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1986-08-01</date><risdate>1986</risdate><volume>46</volume><issue>8</issue><spage>3775</spage><epage>3781</epage><pages>3775-3781</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>We examined androgen modulation of proliferation of clonally derived AXC/SSh rat prostate cancer cells. C-family cells were maintained on medium without addition of androgens. D-family cells were maintained on medium containing 10(-7) M 5 alpha-dihydrotestosterone and T-family cells were maintained on medium containing 10(-7) M testosterone. Proliferation of all AXC/SSh prostate cancer cell lines during propagation on media containing fetal bovine serum was not altered by changes in media testosterone concentration through the range 10(-6) to 10(-9) M. Similarly, proliferation of C- or D-family cell lines, during propagation on media containing steroid depleted, charcoal stripped fetal bovine serum, was not altered by changes in media testosterone concentration through the range 10(-6) to 10(-9) M. By contrast, proliferation of T-family cell lines during propagation on charcoal stripped fetal bovine serum was modulated by androgens; effects were androgen concentration dependent and maximum at 10(-8) to 10(-7) M. Androgens decreased T5 cell proliferation rate and diminished achievable saturation density, whereas T1 cell proliferation rate was increased by androgens. In contrast, T6 cell proliferation rate was unaffected by androgens; however, saturation density was increased. Effects were antagonized by the antiandrogen RU 23908, Anandron, establishing androgen specificity of testosterone or 5 alpha-dihydrotestosterone mediated changes in proliferation.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>2942235</pmid><tpages>7</tpages></addata></record>
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source MEDLINE; American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Androgen Antagonists - pharmacology
Androgens - pharmacology
Animal tumors. Experimental tumors
Animals
Biological and medical sciences
Cell Division - drug effects
Cell Line
Dehydroepiandrosterone - analogs & derivatives
Dehydroepiandrosterone - pharmacology
Dehydroepiandrosterone Sulfate
Experimental renal and urinary tract tumors
Imidazoles - pharmacology
Imidazolidines
Male
Medical sciences
Prostatic Neoplasms - pathology
Rats
Receptors, Androgen - analysis
Testosterone - pharmacology
Tumors
title Differential androgen modulation of AXC/SSh rat prostate cancer cell proliferation in Vitro and its antagonism by antiandrogen
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