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
Hauptverfasser: Garrett, Scott H., Sens, Mary Ann, Shukla, Deepti, Nestor, Scott, Somji, Seema, Todd, John H., Sens, Donald A.
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container_end_page 202
container_issue 3
container_start_page 196
container_title The Prostate
container_volume 41
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
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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&lt;196::AID-PROS7&gt;3.0.CO;2-U</identifier><identifier>PMID: 10517878</identifier><identifier>CODEN: PRSTDS</identifier><language>eng</language><publisher>New York: John Wiley &amp; 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. 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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. 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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. 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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 &amp; Sons, Inc</pub><pmid>10517878</pmid><doi>10.1002/(SICI)1097-0045(19991101)41:3&lt;196::AID-PROS7&gt;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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