Metallothionein isoform 3 expression in the human prostate and cancer-derived cell lines
BACKGROUND Expression of metallothionein isoform 3 (MT‐3) was initially reported to be confined to neural tissues. However, it was recently demonstrated that MT‐3 is expressed in epithelial cells of the human kidney. This motivated the current examination of the expression of MT‐3 in the human prost...
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Veröffentlicht in: | The Prostate 1999-11, Vol.41 (3), p.196-202 |
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creator | Garrett, Scott H. Sens, Mary Ann Shukla, Deepti Nestor, Scott Somji, Seema Todd, John H. Sens, Donald A. |
description | BACKGROUND
Expression of metallothionein isoform 3 (MT‐3) was initially reported to be confined to neural tissues. However, it was recently demonstrated that MT‐3 is expressed in epithelial cells of the human kidney. This motivated the current examination of the expression of MT‐3 in the human prostate.
METHODS
Immunohistochemistry (IHC) was used to localize the expression of MT‐3, RT‐PCR to determine the expression of MT‐3 mRNA, and Western blot analysis to determine the level of MT‐3 protein.
RESULTS
Selected epithelial and stromal cells of the normal human prostate were shown to have low levels of MT‐3 expression. MT‐3 was increased in prostatic intraepithelial neoplasia (PIN) lesions and further increased in a highly variable fashion in prostatic adenocarcinoma. In some adenocarcinomas, MT‐3 expression exceeded that of nerve. Three cell culture models of prostate cancer were also shown to variably express MT‐3. Restriction enzyme analysis confirmed the expression of MT‐3 in the cells and tissues.
CONCLUSIONS
MT‐3 is expressed in the normal human prostate, and expression is enhanced and highly variable in PIN lesions and primary prostate cancer cells. The variable nature of MT‐3 expression was also noted in commonly utilized prostate cancer cell lines. Prostate 41:196–202, 1999. © 1999 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1097-0045(19991101)41:3<196::AID-PROS7>3.0.CO;2-U |
format | Article |
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Expression of metallothionein isoform 3 (MT‐3) was initially reported to be confined to neural tissues. However, it was recently demonstrated that MT‐3 is expressed in epithelial cells of the human kidney. This motivated the current examination of the expression of MT‐3 in the human prostate.
METHODS
Immunohistochemistry (IHC) was used to localize the expression of MT‐3, RT‐PCR to determine the expression of MT‐3 mRNA, and Western blot analysis to determine the level of MT‐3 protein.
RESULTS
Selected epithelial and stromal cells of the normal human prostate were shown to have low levels of MT‐3 expression. MT‐3 was increased in prostatic intraepithelial neoplasia (PIN) lesions and further increased in a highly variable fashion in prostatic adenocarcinoma. In some adenocarcinomas, MT‐3 expression exceeded that of nerve. Three cell culture models of prostate cancer were also shown to variably express MT‐3. Restriction enzyme analysis confirmed the expression of MT‐3 in the cells and tissues.
CONCLUSIONS
MT‐3 is expressed in the normal human prostate, and expression is enhanced and highly variable in PIN lesions and primary prostate cancer cells. The variable nature of MT‐3 expression was also noted in commonly utilized prostate cancer cell lines. Prostate 41:196–202, 1999. © 1999 Wiley‐Liss, Inc.</description><identifier>ISSN: 0270-4137</identifier><identifier>EISSN: 1097-0045</identifier><identifier>DOI: 10.1002/(SICI)1097-0045(19991101)41:3<196::AID-PROS7>3.0.CO;2-U</identifier><identifier>PMID: 10517878</identifier><identifier>CODEN: PRSTDS</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Amino Acid Sequence ; Biological and medical sciences ; cell culture ; Epithelial Cells - physiology ; Gene Expression Regulation, Neoplastic ; Growth Inhibitors - biosynthesis ; Growth Inhibitors - genetics ; Humans ; Immunohistochemistry ; Male ; Medical sciences ; metallothionein isoform 3 ; Molecular Sequence Data ; mRNA ; Nephrology. Urinary tract diseases ; Nerve Tissue Proteins - biosynthesis ; Nerve Tissue Proteins - genetics ; prostate ; prostate cancer ; prostatic intraepithelial neoplasia ; Prostatic Neoplasms - genetics ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - analysis ; RT-PCR ; Tumor Cells, Cultured ; Tumors of the urinary system ; Urinary tract. Prostate gland</subject><ispartof>The Prostate, 1999-11, Vol.41 (3), p.196-202</ispartof><rights>Copyright © 1999 Wiley‐Liss, Inc.</rights><rights>2000 INIST-CNRS</rights><rights>Copyright 1999 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5017-8ca0f9424ee98ecb404a8f57bfe94ccdf67e2b10b369dad46495b8e5dc61a443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291097-0045%2819991101%2941%3A3%3C196%3A%3AAID-PROS7%3E3.0.CO%3B2-U$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291097-0045%2819991101%2941%3A3%3C196%3A%3AAID-PROS7%3E3.0.CO%3B2-U$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1222108$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10517878$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garrett, Scott H.</creatorcontrib><creatorcontrib>Sens, Mary Ann</creatorcontrib><creatorcontrib>Shukla, Deepti</creatorcontrib><creatorcontrib>Nestor, Scott</creatorcontrib><creatorcontrib>Somji, Seema</creatorcontrib><creatorcontrib>Todd, John H.</creatorcontrib><creatorcontrib>Sens, Donald A.</creatorcontrib><title>Metallothionein isoform 3 expression in the human prostate and cancer-derived cell lines</title><title>The Prostate</title><addtitle>Prostate</addtitle><description>BACKGROUND
Expression of metallothionein isoform 3 (MT‐3) was initially reported to be confined to neural tissues. However, it was recently demonstrated that MT‐3 is expressed in epithelial cells of the human kidney. This motivated the current examination of the expression of MT‐3 in the human prostate.
METHODS
Immunohistochemistry (IHC) was used to localize the expression of MT‐3, RT‐PCR to determine the expression of MT‐3 mRNA, and Western blot analysis to determine the level of MT‐3 protein.
RESULTS
Selected epithelial and stromal cells of the normal human prostate were shown to have low levels of MT‐3 expression. MT‐3 was increased in prostatic intraepithelial neoplasia (PIN) lesions and further increased in a highly variable fashion in prostatic adenocarcinoma. In some adenocarcinomas, MT‐3 expression exceeded that of nerve. Three cell culture models of prostate cancer were also shown to variably express MT‐3. Restriction enzyme analysis confirmed the expression of MT‐3 in the cells and tissues.
CONCLUSIONS
MT‐3 is expressed in the normal human prostate, and expression is enhanced and highly variable in PIN lesions and primary prostate cancer cells. The variable nature of MT‐3 expression was also noted in commonly utilized prostate cancer cell lines. Prostate 41:196–202, 1999. © 1999 Wiley‐Liss, Inc.</description><subject>Amino Acid Sequence</subject><subject>Biological and medical sciences</subject><subject>cell culture</subject><subject>Epithelial Cells - physiology</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Growth Inhibitors - biosynthesis</subject><subject>Growth Inhibitors - genetics</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>metallothionein isoform 3</subject><subject>Molecular Sequence Data</subject><subject>mRNA</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>prostate</subject><subject>prostate cancer</subject><subject>prostatic intraepithelial neoplasia</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>RT-PCR</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><issn>0270-4137</issn><issn>1097-0045</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1v0zAUhiMEYmXwF1AuENouUo4dJ44LAk0ZjIqOIrqx3h05yYkayEexU9j-PQ4pAwkkrqzz6vGrV4_nvWIwZQD82dFqns6PGSgZAIjoiCmlGAN2LNgsfMFUPJudzE-DDx-XK_kynMI0XT7nweUdb3L75643AS4hECyUB94Daz8DuG7g970DBhGTiUwm3vqcel3XXb-pupaq1q9sV3am8UOfrreGrHW57_J-Q_5m1-jW35rO9ronX7eFn-s2JxMUZKpv5E6qa7-uWrIPvXulri092r-H3sWb1xfp22CxPJunJ4sgj4DJIMk1lEpwQaQSyjMBQidlJLOSlMjzoowl8YxBFsaq0IWIhYqyhKIij5kWIjz0no61btXXHdkem8oOK3RL3c5irLhMIiEdeDWCuZtvDZW4NVWjzQ0ywME54uAcB384-MNfzlEwDN0VIzrn-NO5CwDTJXK8dM2P9xN2WUPFH72jZAc82QPa5roujXNW2d8c55zBgK1H7HtV081f8_677l_jxsBVB2N1ZXu6vq3W5gvGMpQRXr0_wxV79ylenK7xPPwB5e66pA</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>Garrett, Scott H.</creator><creator>Sens, Mary Ann</creator><creator>Shukla, Deepti</creator><creator>Nestor, Scott</creator><creator>Somji, Seema</creator><creator>Todd, John H.</creator><creator>Sens, Donald A.</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19991101</creationdate><title>Metallothionein isoform 3 expression in the human prostate and cancer-derived cell lines</title><author>Garrett, Scott H. ; Sens, Mary Ann ; Shukla, Deepti ; Nestor, Scott ; Somji, Seema ; Todd, John H. ; Sens, Donald A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5017-8ca0f9424ee98ecb404a8f57bfe94ccdf67e2b10b369dad46495b8e5dc61a443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amino Acid Sequence</topic><topic>Biological and medical sciences</topic><topic>cell culture</topic><topic>Epithelial Cells - physiology</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Growth Inhibitors - biosynthesis</topic><topic>Growth Inhibitors - genetics</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>metallothionein isoform 3</topic><topic>Molecular Sequence Data</topic><topic>mRNA</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nerve Tissue Proteins - biosynthesis</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>prostate</topic><topic>prostate cancer</topic><topic>prostatic intraepithelial neoplasia</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>RT-PCR</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garrett, Scott H.</creatorcontrib><creatorcontrib>Sens, Mary Ann</creatorcontrib><creatorcontrib>Shukla, Deepti</creatorcontrib><creatorcontrib>Nestor, Scott</creatorcontrib><creatorcontrib>Somji, Seema</creatorcontrib><creatorcontrib>Todd, John H.</creatorcontrib><creatorcontrib>Sens, Donald A.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Prostate</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garrett, Scott H.</au><au>Sens, Mary Ann</au><au>Shukla, Deepti</au><au>Nestor, Scott</au><au>Somji, Seema</au><au>Todd, John H.</au><au>Sens, Donald A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metallothionein isoform 3 expression in the human prostate and cancer-derived cell lines</atitle><jtitle>The Prostate</jtitle><addtitle>Prostate</addtitle><date>1999-11-01</date><risdate>1999</risdate><volume>41</volume><issue>3</issue><spage>196</spage><epage>202</epage><pages>196-202</pages><issn>0270-4137</issn><eissn>1097-0045</eissn><coden>PRSTDS</coden><abstract>BACKGROUND
Expression of metallothionein isoform 3 (MT‐3) was initially reported to be confined to neural tissues. However, it was recently demonstrated that MT‐3 is expressed in epithelial cells of the human kidney. This motivated the current examination of the expression of MT‐3 in the human prostate.
METHODS
Immunohistochemistry (IHC) was used to localize the expression of MT‐3, RT‐PCR to determine the expression of MT‐3 mRNA, and Western blot analysis to determine the level of MT‐3 protein.
RESULTS
Selected epithelial and stromal cells of the normal human prostate were shown to have low levels of MT‐3 expression. MT‐3 was increased in prostatic intraepithelial neoplasia (PIN) lesions and further increased in a highly variable fashion in prostatic adenocarcinoma. In some adenocarcinomas, MT‐3 expression exceeded that of nerve. Three cell culture models of prostate cancer were also shown to variably express MT‐3. Restriction enzyme analysis confirmed the expression of MT‐3 in the cells and tissues.
CONCLUSIONS
MT‐3 is expressed in the normal human prostate, and expression is enhanced and highly variable in PIN lesions and primary prostate cancer cells. The variable nature of MT‐3 expression was also noted in commonly utilized prostate cancer cell lines. Prostate 41:196–202, 1999. © 1999 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10517878</pmid><doi>10.1002/(SICI)1097-0045(19991101)41:3<196::AID-PROS7>3.0.CO;2-U</doi><tpages>7</tpages></addata></record> |
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subjects | Amino Acid Sequence Biological and medical sciences cell culture Epithelial Cells - physiology Gene Expression Regulation, Neoplastic Growth Inhibitors - biosynthesis Growth Inhibitors - genetics Humans Immunohistochemistry Male Medical sciences metallothionein isoform 3 Molecular Sequence Data mRNA Nephrology. Urinary tract diseases Nerve Tissue Proteins - biosynthesis Nerve Tissue Proteins - genetics prostate prostate cancer prostatic intraepithelial neoplasia Prostatic Neoplasms - genetics Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - analysis RT-PCR Tumor Cells, Cultured Tumors of the urinary system Urinary tract. Prostate gland |
title | Metallothionein isoform 3 expression in the human prostate and cancer-derived cell lines |
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