Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer

The expression level of the androgen receptor (AR) gene in androgen-dependent and -independent prostate cancer was determined by using real-time quantitative reverse transcription-PCR assay. Eight benign prostate hyperplasias, 33 untreated and 13 hormone-refractory locally recurrent carcinomas, as w...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer research (Baltimore) 2001-05, Vol.61 (9), p.3550-3555
Hauptverfasser: LINJA, Marika J, SAVINAINEN, Kimmo J, SARAMÄKI, Outi R, TAMMELA, Teuvo L. J, VESSELLA, Robert L, VISAKORPI, Tapio
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3555
container_issue 9
container_start_page 3550
container_title Cancer research (Baltimore)
container_volume 61
creator LINJA, Marika J
SAVINAINEN, Kimmo J
SARAMÄKI, Outi R
TAMMELA, Teuvo L. J
VESSELLA, Robert L
VISAKORPI, Tapio
description The expression level of the androgen receptor (AR) gene in androgen-dependent and -independent prostate cancer was determined by using real-time quantitative reverse transcription-PCR assay. Eight benign prostate hyperplasias, 33 untreated and 13 hormone-refractory locally recurrent carcinomas, as well as 10 prostate cancer xenografts, were analyzed. All hormone-refractory tumors expressed AR and showed, on average, 6-fold higher expression than androgen-dependent tumors or benign prostate hyperplasias (P < 0.001). Four of 13 (31%) hormone-refractory tumors contained AR gene amplification detected by fluorescence in situ hybridization. Androgen-independent tumors with gene amplification expressed, on average, a 2-fold higher level of AR than the refractory tumors without the gene amplification. Two xenografts (LuCaP 35 and 69) showed amplification and high-level expression of the AR gene. These xenografts are the first prostate cancer model systems containing the gene amplification. The findings demonstrate that AR is highly expressed in androgen-independent prostate cancer, suggesting that the AR signaling pathway is important in the progression of prostate cancer during endocrine treatment. The two xenografts with the AR gene amplification will enable studies evaluating the functional significance of the amplification and development of new treatment strategies based on high-level expression of AR.
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_70814545</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>17896674</sourcerecordid><originalsourceid>FETCH-LOGICAL-h299t-2e88a0f278b39c21222953954851db31decb97c4954d2cc0e685c65d389814343</originalsourceid><addsrcrecordid>eNqFkE9LAzEUxIMotla_ggQEbwv5u5scS1ErFLzoec1m39rIbrImW7Hf3hSrV0-PmfkxD-YEzankqqiEkKdoTghRhRQVm6GLlN6zlJTIczSjlDOpaDlHr8th7F3nrJlc8Nj4FodPiPA1RkjpYIXu4MbwBh5HsDBOIeIsADuPtyEOwUMRoYvG5mSPxxjSZCbA1ngL8RKddaZPcHW8C_Ryf_e8Whebp4fH1XJTbJnWU8FAKUM6VqmGa8soY0xLrqVQkrYNpy3YRldWZKdl1hIolbSlbLnSigou-ALd_vTm_x87SFM9uGSh742HsEt1RTInhfwXpJXSZVkdGq-P4K4ZoK3H6AYT9_XveBm4OQImWdPnBbx16Y_TWpKS8W_Z8XkF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17896674</pqid></control><display><type>article</type><title>Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer</title><source>MEDLINE</source><source>American Association for Cancer Research</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>LINJA, Marika J ; SAVINAINEN, Kimmo J ; SARAMÄKI, Outi R ; TAMMELA, Teuvo L. J ; VESSELLA, Robert L ; VISAKORPI, Tapio</creator><creatorcontrib>LINJA, Marika J ; SAVINAINEN, Kimmo J ; SARAMÄKI, Outi R ; TAMMELA, Teuvo L. J ; VESSELLA, Robert L ; VISAKORPI, Tapio</creatorcontrib><description>The expression level of the androgen receptor (AR) gene in androgen-dependent and -independent prostate cancer was determined by using real-time quantitative reverse transcription-PCR assay. Eight benign prostate hyperplasias, 33 untreated and 13 hormone-refractory locally recurrent carcinomas, as well as 10 prostate cancer xenografts, were analyzed. All hormone-refractory tumors expressed AR and showed, on average, 6-fold higher expression than androgen-dependent tumors or benign prostate hyperplasias (P &lt; 0.001). Four of 13 (31%) hormone-refractory tumors contained AR gene amplification detected by fluorescence in situ hybridization. Androgen-independent tumors with gene amplification expressed, on average, a 2-fold higher level of AR than the refractory tumors without the gene amplification. Two xenografts (LuCaP 35 and 69) showed amplification and high-level expression of the AR gene. These xenografts are the first prostate cancer model systems containing the gene amplification. The findings demonstrate that AR is highly expressed in androgen-independent prostate cancer, suggesting that the AR signaling pathway is important in the progression of prostate cancer during endocrine treatment. The two xenografts with the AR gene amplification will enable studies evaluating the functional significance of the amplification and development of new treatment strategies based on high-level expression of AR.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 11325816</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Animals ; Biological and medical sciences ; Gene Amplification ; Gene Dosage ; Gene Expression ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Medical sciences ; Mice ; Neoplasms, Hormone-Dependent - genetics ; Neoplasms, Hormone-Dependent - metabolism ; Nephrology. Urinary tract diseases ; Prostate-Specific Antigen - biosynthesis ; Prostate-Specific Antigen - genetics ; Prostatic Hyperplasia - genetics ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - metabolism ; Receptors, Androgen - biosynthesis ; Receptors, Androgen - genetics ; Reverse Transcriptase Polymerase Chain Reaction ; Tumors of the urinary system ; Urinary tract. Prostate gland</subject><ispartof>Cancer research (Baltimore), 2001-05, Vol.61 (9), p.3550-3555</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,776,780,785,786,23909,23910,25118</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=995062$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11325816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LINJA, Marika J</creatorcontrib><creatorcontrib>SAVINAINEN, Kimmo J</creatorcontrib><creatorcontrib>SARAMÄKI, Outi R</creatorcontrib><creatorcontrib>TAMMELA, Teuvo L. J</creatorcontrib><creatorcontrib>VESSELLA, Robert L</creatorcontrib><creatorcontrib>VISAKORPI, Tapio</creatorcontrib><title>Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer</title><title>Cancer research (Baltimore)</title><addtitle>Cancer Res</addtitle><description>The expression level of the androgen receptor (AR) gene in androgen-dependent and -independent prostate cancer was determined by using real-time quantitative reverse transcription-PCR assay. Eight benign prostate hyperplasias, 33 untreated and 13 hormone-refractory locally recurrent carcinomas, as well as 10 prostate cancer xenografts, were analyzed. All hormone-refractory tumors expressed AR and showed, on average, 6-fold higher expression than androgen-dependent tumors or benign prostate hyperplasias (P &lt; 0.001). Four of 13 (31%) hormone-refractory tumors contained AR gene amplification detected by fluorescence in situ hybridization. Androgen-independent tumors with gene amplification expressed, on average, a 2-fold higher level of AR than the refractory tumors without the gene amplification. Two xenografts (LuCaP 35 and 69) showed amplification and high-level expression of the AR gene. These xenografts are the first prostate cancer model systems containing the gene amplification. The findings demonstrate that AR is highly expressed in androgen-independent prostate cancer, suggesting that the AR signaling pathway is important in the progression of prostate cancer during endocrine treatment. The two xenografts with the AR gene amplification will enable studies evaluating the functional significance of the amplification and development of new treatment strategies based on high-level expression of AR.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Gene Amplification</subject><subject>Gene Dosage</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Neoplasms, Hormone-Dependent - genetics</subject><subject>Neoplasms, Hormone-Dependent - metabolism</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Prostate-Specific Antigen - biosynthesis</subject><subject>Prostate-Specific Antigen - genetics</subject><subject>Prostatic Hyperplasia - genetics</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Receptors, Androgen - biosynthesis</subject><subject>Receptors, Androgen - genetics</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9LAzEUxIMotla_ggQEbwv5u5scS1ErFLzoec1m39rIbrImW7Hf3hSrV0-PmfkxD-YEzankqqiEkKdoTghRhRQVm6GLlN6zlJTIczSjlDOpaDlHr8th7F3nrJlc8Nj4FodPiPA1RkjpYIXu4MbwBh5HsDBOIeIsADuPtyEOwUMRoYvG5mSPxxjSZCbA1ngL8RKddaZPcHW8C_Ryf_e8Whebp4fH1XJTbJnWU8FAKUM6VqmGa8soY0xLrqVQkrYNpy3YRldWZKdl1hIolbSlbLnSigou-ALd_vTm_x87SFM9uGSh742HsEt1RTInhfwXpJXSZVkdGq-P4K4ZoK3H6AYT9_XveBm4OQImWdPnBbx16Y_TWpKS8W_Z8XkF</recordid><startdate>20010501</startdate><enddate>20010501</enddate><creator>LINJA, Marika J</creator><creator>SAVINAINEN, Kimmo J</creator><creator>SARAMÄKI, Outi R</creator><creator>TAMMELA, Teuvo L. J</creator><creator>VESSELLA, Robert L</creator><creator>VISAKORPI, Tapio</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>20010501</creationdate><title>Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer</title><author>LINJA, Marika J ; SAVINAINEN, Kimmo J ; SARAMÄKI, Outi R ; TAMMELA, Teuvo L. J ; VESSELLA, Robert L ; VISAKORPI, Tapio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h299t-2e88a0f278b39c21222953954851db31decb97c4954d2cc0e685c65d389814343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Gene Amplification</topic><topic>Gene Dosage</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Neoplasms, Hormone-Dependent - genetics</topic><topic>Neoplasms, Hormone-Dependent - metabolism</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Prostate-Specific Antigen - biosynthesis</topic><topic>Prostate-Specific Antigen - genetics</topic><topic>Prostatic Hyperplasia - genetics</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Receptors, Androgen - biosynthesis</topic><topic>Receptors, Androgen - genetics</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LINJA, Marika J</creatorcontrib><creatorcontrib>SAVINAINEN, Kimmo J</creatorcontrib><creatorcontrib>SARAMÄKI, Outi R</creatorcontrib><creatorcontrib>TAMMELA, Teuvo L. J</creatorcontrib><creatorcontrib>VESSELLA, Robert L</creatorcontrib><creatorcontrib>VISAKORPI, Tapio</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LINJA, Marika J</au><au>SAVINAINEN, Kimmo J</au><au>SARAMÄKI, Outi R</au><au>TAMMELA, Teuvo L. J</au><au>VESSELLA, Robert L</au><au>VISAKORPI, Tapio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer</atitle><jtitle>Cancer research (Baltimore)</jtitle><addtitle>Cancer Res</addtitle><date>2001-05-01</date><risdate>2001</risdate><volume>61</volume><issue>9</issue><spage>3550</spage><epage>3555</epage><pages>3550-3555</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>The expression level of the androgen receptor (AR) gene in androgen-dependent and -independent prostate cancer was determined by using real-time quantitative reverse transcription-PCR assay. Eight benign prostate hyperplasias, 33 untreated and 13 hormone-refractory locally recurrent carcinomas, as well as 10 prostate cancer xenografts, were analyzed. All hormone-refractory tumors expressed AR and showed, on average, 6-fold higher expression than androgen-dependent tumors or benign prostate hyperplasias (P &lt; 0.001). Four of 13 (31%) hormone-refractory tumors contained AR gene amplification detected by fluorescence in situ hybridization. Androgen-independent tumors with gene amplification expressed, on average, a 2-fold higher level of AR than the refractory tumors without the gene amplification. Two xenografts (LuCaP 35 and 69) showed amplification and high-level expression of the AR gene. These xenografts are the first prostate cancer model systems containing the gene amplification. The findings demonstrate that AR is highly expressed in androgen-independent prostate cancer, suggesting that the AR signaling pathway is important in the progression of prostate cancer during endocrine treatment. The two xenografts with the AR gene amplification will enable studies evaluating the functional significance of the amplification and development of new treatment strategies based on high-level expression of AR.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>11325816</pmid><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0008-5472
ispartof Cancer research (Baltimore), 2001-05, Vol.61 (9), p.3550-3555
issn 0008-5472
1538-7445
language eng
recordid cdi_proquest_miscellaneous_70814545
source MEDLINE; American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Animals
Biological and medical sciences
Gene Amplification
Gene Dosage
Gene Expression
Humans
In Situ Hybridization, Fluorescence
Male
Medical sciences
Mice
Neoplasms, Hormone-Dependent - genetics
Neoplasms, Hormone-Dependent - metabolism
Nephrology. Urinary tract diseases
Prostate-Specific Antigen - biosynthesis
Prostate-Specific Antigen - genetics
Prostatic Hyperplasia - genetics
Prostatic Neoplasms - genetics
Prostatic Neoplasms - metabolism
Receptors, Androgen - biosynthesis
Receptors, Androgen - genetics
Reverse Transcriptase Polymerase Chain Reaction
Tumors of the urinary system
Urinary tract. Prostate gland
title Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-20T20%3A53%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amplification%20and%20overexpression%20of%20androgen%20receptor%20gene%20in%20hormone-refractory%20prostate%20cancer&rft.jtitle=Cancer%20research%20(Baltimore)&rft.au=LINJA,%20Marika%20J&rft.date=2001-05-01&rft.volume=61&rft.issue=9&rft.spage=3550&rft.epage=3555&rft.pages=3550-3555&rft.issn=0008-5472&rft.eissn=1538-7445&rft.coden=CNREA8&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E17896674%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17896674&rft_id=info:pmid/11325816&rfr_iscdi=true