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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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. 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.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2007.12.012</identifier><identifier>PMID: 18547613</identifier><identifier>CODEN: HPCQA4</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>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</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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20569385$$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. 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.</description><subject>Biological and medical sciences</subject><subject>Bladder</subject><subject>Cell cycle</subject><subject>Cyclin-Dependent Kinase Inhibitor p16</subject><subject>Female</subject><subject>Genes</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>IMP3</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Kinases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mutation</subject><subject>Neoplasm Proteins - analysis</subject><subject>p16</subject><subject>p53</subject><subject>Pathology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Proteins</subject><subject>RNA-Binding Proteins - analysis</subject><subject>Rodents</subject><subject>Tumor Suppressor Protein p53 - analysis</subject><subject>Tumors</subject><subject>Urologic Neoplasms - chemistry</subject><subject>Urologic Neoplasms - pathology</subject><subject>Urothelial neoplasia</subject><subject>Urothelium - chemistry</subject><subject>Urothelium - pathology</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkktv1DAUhS0EokPhJ4AsIRAsEvyMnQ2oGhWoKBTxEEvLcW46nibOYCeI_ns8mqiVumFlXfk7x8dHF6GnlJSU0OrNttzMw85Om5IRokrKSkLZPbSikrNC85rdRytCRFVoqtQRepTSlhBKpZAP0RHVUqiK8hX6dfp3FyElPwY8dvjbl5Oi8aH14RLv4jiBD_js81eOX326WL_GeWog-MuA53y5gd7PA7ahvRltj6d5GGN6jB50tk_wZDmP0c_3pz_WH4vziw9n65PzwknBpsIxkJVTAmQrW81owzvauUqTumkpE1IQbWtlG0W6TmkraCtco0FLBZXIDD9GLw--Oe3vGdJkBp8c9L0NMM7JVDWXohZ1Bp_fAbfjHEPOZijhQiupuM6UPFAujilF6Mwu-sHG6wyZfe9ma5bezb53Q5nJvWfds8V9bgZob1VL0Rl4sQA2Odt30Qbn0w3HiMxJtczcuwMHubQ_HqJJzkNw0PoIbjLt6P8b5e0dB9f74POjV3AN6fbXJmWB-b5fkv2OEJVNqBL8H3fUtuk</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>Li, Lin, MD</creator><creator>Xu, Haodong, MD, PhD</creator><creator>Spaulding, Betsy O., BS</creator><creator>Cheng, Liang, MD</creator><creator>Simon, Rochelle, MD</creator><creator>Yao, Jorge L., MD</creator><creator>di Sant'Agnese, P. Anthony, MD</creator><creator>Bourne, Patricia A., BS</creator><creator>Huang, Jiaoti, MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>20080801</creationdate><title>Expression of RNA-binding protein IMP3 (KOC) in benign urothelium and urothelial tumors</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c542t-c2e56c74e5d5d821b3f1fc6809bd1245408a97ab70ff78a41d4cb8e857e649bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Biological and medical sciences</topic><topic>Bladder</topic><topic>Cell cycle</topic><topic>Cyclin-Dependent Kinase Inhibitor p16</topic><topic>Female</topic><topic>Genes</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>IMP3</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Kinases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mutation</topic><topic>Neoplasm Proteins - analysis</topic><topic>p16</topic><topic>p53</topic><topic>Pathology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Proteins</topic><topic>RNA-Binding Proteins - analysis</topic><topic>Rodents</topic><topic>Tumor Suppressor Protein p53 - analysis</topic><topic>Tumors</topic><topic>Urologic Neoplasms - chemistry</topic><topic>Urologic Neoplasms - pathology</topic><topic>Urothelial neoplasia</topic><topic>Urothelium - chemistry</topic><topic>Urothelium - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><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>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Lin, MD</au><au>Xu, Haodong, MD, PhD</au><au>Spaulding, Betsy O., BS</au><au>Cheng, Liang, MD</au><au>Simon, Rochelle, MD</au><au>Yao, Jorge L., MD</au><au>di Sant'Agnese, P. 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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