Expression of RNA-binding protein IMP3 (KOC) in benign urothelium and urothelial tumors

Summary RNA-binding protein IMP3 is a KH-domain–containing protein and a member of the insulin-like growth factor messenger RNA–binding protein family. It is identical to K-homology protein overexpressed in cancer that was identified through screening for genes differentially expressed between benig...

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Veröffentlicht in:Human pathology 2008-08, Vol.39 (8), p.1205-1211
Hauptverfasser: Li, Lin, MD, Xu, Haodong, MD, PhD, Spaulding, Betsy O., BS, Cheng, Liang, MD, Simon, Rochelle, MD, Yao, Jorge L., MD, di Sant'Agnese, P. Anthony, MD, Bourne, Patricia A., BS, Huang, Jiaoti, MD, PhD
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container_end_page 1211
container_issue 8
container_start_page 1205
container_title Human pathology
container_volume 39
creator Li, Lin, MD
Xu, Haodong, MD, PhD
Spaulding, Betsy O., BS
Cheng, Liang, MD
Simon, Rochelle, MD
Yao, Jorge L., MD
di Sant'Agnese, P. Anthony, MD
Bourne, Patricia A., BS
Huang, Jiaoti, MD, PhD
description Summary RNA-binding protein IMP3 is a KH-domain–containing protein and a member of the insulin-like growth factor messenger RNA–binding protein family. It is identical to K-homology protein overexpressed in cancer that was identified through screening for genes differentially expressed between benign pancreatic tissue and pancreatic cancer. Several studies have shown that IMP3 is associated with aggressive and advanced tumors in various organs. We studied the expression of IMP3 in benign urothelium and urothelial tumors by immunohistochemistry. The expression pattern of IMP3 was further compared with that of p53 and p16. Our study shows that IMP3 is generally not expressed in benign urothelium or low-grade urothelial tumors including urothelial dysplasia, papillary urothelial neoplasm of low malignant potential, and low-grade papillary urothelial carcinoma. The expression of IMP3 is significantly increased in high-grade urothelial tumors including high-grade papillary urothelial carcinoma, urothelial carcinoma in situ, and invasive urothelial carcinoma. Expression of IMP3 in urothelial tumors parallels the accumulation of nuclear p53, although there is not always a one to one correlation. In contrast, expression of p16 in the different groups of urothelial tumors is more variable. Urothelial carcinomas with invasion of muscularis propria appear to express IMP3 more frequently than lower-stage tumors. These findings suggest that IMP3 may be involved in the progression of urothelial tumors from low grade to high grade in both papillary and flat lesions. Immunohistochemical detection of the combined expression of IMP3 and p53 is useful in the diagnosis of high-grade urothelial tumors, particularly in small, superficial materials.
doi_str_mv 10.1016/j.humpath.2007.12.012
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Anthony, MD ; Bourne, Patricia A., BS ; Huang, Jiaoti, MD, PhD</creator><creatorcontrib>Li, Lin, MD ; Xu, Haodong, MD, PhD ; Spaulding, Betsy O., BS ; Cheng, Liang, MD ; Simon, Rochelle, MD ; Yao, Jorge L., MD ; di Sant'Agnese, P. Anthony, MD ; Bourne, Patricia A., BS ; Huang, Jiaoti, MD, PhD</creatorcontrib><description>Summary RNA-binding protein IMP3 is a KH-domain–containing protein and a member of the insulin-like growth factor messenger RNA–binding protein family. It is identical to K-homology protein overexpressed in cancer that was identified through screening for genes differentially expressed between benign pancreatic tissue and pancreatic cancer. Several studies have shown that IMP3 is associated with aggressive and advanced tumors in various organs. We studied the expression of IMP3 in benign urothelium and urothelial tumors by immunohistochemistry. The expression pattern of IMP3 was further compared with that of p53 and p16. Our study shows that IMP3 is generally not expressed in benign urothelium or low-grade urothelial tumors including urothelial dysplasia, papillary urothelial neoplasm of low malignant potential, and low-grade papillary urothelial carcinoma. The expression of IMP3 is significantly increased in high-grade urothelial tumors including high-grade papillary urothelial carcinoma, urothelial carcinoma in situ, and invasive urothelial carcinoma. Expression of IMP3 in urothelial tumors parallels the accumulation of nuclear p53, although there is not always a one to one correlation. In contrast, expression of p16 in the different groups of urothelial tumors is more variable. Urothelial carcinomas with invasion of muscularis propria appear to express IMP3 more frequently than lower-stage tumors. These findings suggest that IMP3 may be involved in the progression of urothelial tumors from low grade to high grade in both papillary and flat lesions. 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Miscellaneous investigative techniques ; Proteins ; RNA-Binding Proteins - analysis ; Rodents ; Tumor Suppressor Protein p53 - analysis ; Tumors ; Urologic Neoplasms - chemistry ; Urologic Neoplasms - pathology ; Urothelial neoplasia ; Urothelium - chemistry ; Urothelium - pathology</subject><ispartof>Human pathology, 2008-08, Vol.39 (8), p.1205-1211</ispartof><rights>Elsevier Inc.</rights><rights>2008 Elsevier Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-c2e56c74e5d5d821b3f1fc6809bd1245408a97ab70ff78a41d4cb8e857e649bd3</citedby><cites>FETCH-LOGICAL-c542t-c2e56c74e5d5d821b3f1fc6809bd1245408a97ab70ff78a41d4cb8e857e649bd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0046817707007174$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20569385$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18547613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Lin, MD</creatorcontrib><creatorcontrib>Xu, Haodong, MD, PhD</creatorcontrib><creatorcontrib>Spaulding, Betsy O., BS</creatorcontrib><creatorcontrib>Cheng, Liang, MD</creatorcontrib><creatorcontrib>Simon, Rochelle, MD</creatorcontrib><creatorcontrib>Yao, Jorge L., MD</creatorcontrib><creatorcontrib>di Sant'Agnese, P. Anthony, MD</creatorcontrib><creatorcontrib>Bourne, Patricia A., BS</creatorcontrib><creatorcontrib>Huang, Jiaoti, MD, PhD</creatorcontrib><title>Expression of RNA-binding protein IMP3 (KOC) in benign urothelium and urothelial tumors</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>Summary RNA-binding protein IMP3 is a KH-domain–containing protein and a member of the insulin-like growth factor messenger RNA–binding protein family. It is identical to K-homology protein overexpressed in cancer that was identified through screening for genes differentially expressed between benign pancreatic tissue and pancreatic cancer. Several studies have shown that IMP3 is associated with aggressive and advanced tumors in various organs. We studied the expression of IMP3 in benign urothelium and urothelial tumors by immunohistochemistry. The expression pattern of IMP3 was further compared with that of p53 and p16. Our study shows that IMP3 is generally not expressed in benign urothelium or low-grade urothelial tumors including urothelial dysplasia, papillary urothelial neoplasm of low malignant potential, and low-grade papillary urothelial carcinoma. The expression of IMP3 is significantly increased in high-grade urothelial tumors including high-grade papillary urothelial carcinoma, urothelial carcinoma in situ, and invasive urothelial carcinoma. Expression of IMP3 in urothelial tumors parallels the accumulation of nuclear p53, although there is not always a one to one correlation. In contrast, expression of p16 in the different groups of urothelial tumors is more variable. Urothelial carcinomas with invasion of muscularis propria appear to express IMP3 more frequently than lower-stage tumors. These findings suggest that IMP3 may be involved in the progression of urothelial tumors from low grade to high grade in both papillary and flat lesions. 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Anthony, MD</au><au>Bourne, Patricia A., BS</au><au>Huang, Jiaoti, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of RNA-binding protein IMP3 (KOC) in benign urothelium and urothelial tumors</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>39</volume><issue>8</issue><spage>1205</spage><epage>1211</epage><pages>1205-1211</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><coden>HPCQA4</coden><abstract>Summary RNA-binding protein IMP3 is a KH-domain–containing protein and a member of the insulin-like growth factor messenger RNA–binding protein family. It is identical to K-homology protein overexpressed in cancer that was identified through screening for genes differentially expressed between benign pancreatic tissue and pancreatic cancer. Several studies have shown that IMP3 is associated with aggressive and advanced tumors in various organs. We studied the expression of IMP3 in benign urothelium and urothelial tumors by immunohistochemistry. The expression pattern of IMP3 was further compared with that of p53 and p16. Our study shows that IMP3 is generally not expressed in benign urothelium or low-grade urothelial tumors including urothelial dysplasia, papillary urothelial neoplasm of low malignant potential, and low-grade papillary urothelial carcinoma. The expression of IMP3 is significantly increased in high-grade urothelial tumors including high-grade papillary urothelial carcinoma, urothelial carcinoma in situ, and invasive urothelial carcinoma. Expression of IMP3 in urothelial tumors parallels the accumulation of nuclear p53, although there is not always a one to one correlation. In contrast, expression of p16 in the different groups of urothelial tumors is more variable. Urothelial carcinomas with invasion of muscularis propria appear to express IMP3 more frequently than lower-stage tumors. These findings suggest that IMP3 may be involved in the progression of urothelial tumors from low grade to high grade in both papillary and flat lesions. Immunohistochemical detection of the combined expression of IMP3 and p53 is useful in the diagnosis of high-grade urothelial tumors, particularly in small, superficial materials.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>18547613</pmid><doi>10.1016/j.humpath.2007.12.012</doi><tpages>7</tpages></addata></record>
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subjects Biological and medical sciences
Bladder
Cell cycle
Cyclin-Dependent Kinase Inhibitor p16
Female
Genes
Humans
Immunohistochemistry
IMP3
Investigative techniques, diagnostic techniques (general aspects)
Kinases
Male
Medical sciences
Mutation
Neoplasm Proteins - analysis
p16
p53
Pathology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Proteins
RNA-Binding Proteins - analysis
Rodents
Tumor Suppressor Protein p53 - analysis
Tumors
Urologic Neoplasms - chemistry
Urologic Neoplasms - pathology
Urothelial neoplasia
Urothelium - chemistry
Urothelium - pathology
title Expression of RNA-binding protein IMP3 (KOC) in benign urothelium and urothelial tumors
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