Immunohistochemical localization of glutathione S-transferase-pi in human colorectal polyps

AIM: To investigate the distribution of the placental form of glutathione-S-transferase (GST) in colon polyps in order to evaluate the role of GST-pi in these tissues. METHODS: Sixteen polyp tissues removed at colon- oscopy were examined. Tissues were investigated his- tologically and ultrastructura...

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Veröffentlicht in:World journal of gastroenterology : WJG 2008-07, Vol.14 (26), p.4179-4184
Hauptverfasser: Gaitanarou, Eleni, Seretis, Eleni, Xinopoulos, Dimitrios, Paraskevas, Emmanuel, Arnoyiannaki, Niki, Voloudakis-Baltatzis, Irene
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container_end_page 4184
container_issue 26
container_start_page 4179
container_title World journal of gastroenterology : WJG
container_volume 14
creator Gaitanarou, Eleni
Seretis, Eleni
Xinopoulos, Dimitrios
Paraskevas, Emmanuel
Arnoyiannaki, Niki
Voloudakis-Baltatzis, Irene
description AIM: To investigate the distribution of the placental form of glutathione-S-transferase (GST) in colon polyps in order to evaluate the role of GST-pi in these tissues. METHODS: Sixteen polyp tissues removed at colon- oscopy were examined. Tissues were investigated his- tologically and ultrastructurally. GST-pi expression was also analysed immunohistochemically, using peroxidase anti-peroxidase (PAP) method and immunogold label- ling method, for light and electron microscope respec- tively. RESULTS: All polyp tissues examined were adenoma of low, mild and high- grade dysplasia as shown in the histopathological reports. Nevertheless, the examina- tion of the above specimens with electron microscope revealed that 3 of 9 adenoma of mild dysplasia had ultrastuctural features similar to high-grade dysplasia adenoma. GST-pi was variably expressed in adenoma, with the lowest relative levels occurring in low-grade adenoma and the highest levels found in high-grade adenoma. GST-pi was located mainly in undifferentiat- ed epithelial cells. GST-pi positive particles were found in the cytoplasm and especially in the nucleus adjacent to the nuclear membrane of these cells. CONCLUSION: The overexpression of GST-pi in mild- grade adenomas with significant subcellular changes and in the majority of high-grade dysplasia adenoma suggests that this might be related to the carcinogenetic proceeding. Immunohistochemical localization of GST-pi in combination with ultrastructural changes indicate that GST-pi might be a sensitive agent for the detection of preneoplastic transformations in adenoma.
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METHODS: Sixteen polyp tissues removed at colon- oscopy were examined. Tissues were investigated his- tologically and ultrastructurally. GST-pi expression was also analysed immunohistochemically, using peroxidase anti-peroxidase (PAP) method and immunogold label- ling method, for light and electron microscope respec- tively. RESULTS: All polyp tissues examined were adenoma of low, mild and high- grade dysplasia as shown in the histopathological reports. Nevertheless, the examina- tion of the above specimens with electron microscope revealed that 3 of 9 adenoma of mild dysplasia had ultrastuctural features similar to high-grade dysplasia adenoma. GST-pi was variably expressed in adenoma, with the lowest relative levels occurring in low-grade adenoma and the highest levels found in high-grade adenoma. GST-pi was located mainly in undifferentiat- ed epithelial cells. GST-pi positive particles were found in the cytoplasm and especially in the nucleus adjacent to the nuclear membrane of these cells. CONCLUSION: The overexpression of GST-pi in mild- grade adenomas with significant subcellular changes and in the majority of high-grade dysplasia adenoma suggests that this might be related to the carcinogenetic proceeding. Immunohistochemical localization of GST-pi in combination with ultrastructural changes indicate that GST-pi might be a sensitive agent for the detection of preneoplastic transformations in adenoma.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.14.4179</identifier><identifier>PMID: 18636663</identifier><language>eng</language><publisher>United States: Department of Electron Microscopy-Cell Biology, "G. Papanicolaou" Research Center of Oncology and Experimental Surgery, "Agios Sawas" Anticancer Hospital of Athens, Athens 11522, Greece%Department of Gastroenterology, "Agios Savvas" Anticancer Hospital of Athens, Athens 11522, Greece%Department of Pathology of the Regional Anticancer-Oncologic Hospital of Athens "Agios Savvas", Athens 11522, Greece</publisher><subject>Adenoma - enzymology ; Basic Research ; Colonic Neoplasms - enzymology ; Colonic Polyps - enzymology ; Colonic Polyps - pathology ; Colonic Polyps - ultrastructure ; Glutathione S-Transferase pi - analysis ; Humans ; Immunohistochemistry ; Microscopy, Electron ; 免疫组织化学 ; 电子显微镜 ; 结肠直肠息肉</subject><ispartof>World journal of gastroenterology : WJG, 2008-07, Vol.14 (26), p.4179-4184</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><rights>2008 The WJG Press and Baishideng. All rights reserved. 2008</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-cbf2cb0a2ffb4439ed79e9c60642a3a3a1cdd52a1fcb8825af9c98ef8a09d9fc3</citedby><cites>FETCH-LOGICAL-c435t-cbf2cb0a2ffb4439ed79e9c60642a3a3a1cdd52a1fcb8825af9c98ef8a09d9fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2725379/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2725379/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18636663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gaitanarou, Eleni</creatorcontrib><creatorcontrib>Seretis, Eleni</creatorcontrib><creatorcontrib>Xinopoulos, Dimitrios</creatorcontrib><creatorcontrib>Paraskevas, Emmanuel</creatorcontrib><creatorcontrib>Arnoyiannaki, Niki</creatorcontrib><creatorcontrib>Voloudakis-Baltatzis, Irene</creatorcontrib><title>Immunohistochemical localization of glutathione S-transferase-pi in human colorectal polyps</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To investigate the distribution of the placental form of glutathione-S-transferase (GST) in colon polyps in order to evaluate the role of GST-pi in these tissues. METHODS: Sixteen polyp tissues removed at colon- oscopy were examined. Tissues were investigated his- tologically and ultrastructurally. GST-pi expression was also analysed immunohistochemically, using peroxidase anti-peroxidase (PAP) method and immunogold label- ling method, for light and electron microscope respec- tively. RESULTS: All polyp tissues examined were adenoma of low, mild and high- grade dysplasia as shown in the histopathological reports. Nevertheless, the examina- tion of the above specimens with electron microscope revealed that 3 of 9 adenoma of mild dysplasia had ultrastuctural features similar to high-grade dysplasia adenoma. GST-pi was variably expressed in adenoma, with the lowest relative levels occurring in low-grade adenoma and the highest levels found in high-grade adenoma. GST-pi was located mainly in undifferentiat- ed epithelial cells. GST-pi positive particles were found in the cytoplasm and especially in the nucleus adjacent to the nuclear membrane of these cells. CONCLUSION: The overexpression of GST-pi in mild- grade adenomas with significant subcellular changes and in the majority of high-grade dysplasia adenoma suggests that this might be related to the carcinogenetic proceeding. Immunohistochemical localization of GST-pi in combination with ultrastructural changes indicate that GST-pi might be a sensitive agent for the detection of preneoplastic transformations in adenoma.</description><subject>Adenoma - enzymology</subject><subject>Basic Research</subject><subject>Colonic Neoplasms - enzymology</subject><subject>Colonic Polyps - enzymology</subject><subject>Colonic Polyps - pathology</subject><subject>Colonic Polyps - ultrastructure</subject><subject>Glutathione S-Transferase pi - analysis</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Microscopy, Electron</subject><subject>免疫组织化学</subject><subject>电子显微镜</subject><subject>结肠直肠息肉</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctL5TAUh4M46PWxci9FZie95tVHNoKILxBmMbpyEU7TpM21TWrTjjh__eRyL-oQSDjk4zs_zkHohOAlK3h58b5qloQvOSnEDlpQSkRKS4530YJgXKSC0WIfHYSwwpgyltE9tE_KnOV5zhbo5aHvZ-dbGyavWt1bBV3S-XjbvzBZ7xJvkqabJ5jaWOnkdzqN4ILRIwSdDjaxLmnnHlyifOdHraYoGHz3MYQj9MNAF_Tx9j1Ez7c3T9f36eOvu4frq8dUcZZNqaoMVRUGakzFORO6LoQWKsc5p8DiIaquMwrEqKosaQZGKFFqUwIWtTCKHaLLjXeYq17XSrsYsZPDaHsYP6QHK___cbaVjf8jaUEzVogo-LkRvIMz4Bq58vPoYmQZZ0sxLmmOCY3Y-QZTow9h1OazBcFyvYo1LgmX61VE-vR7qi92O_sInG11rXfNm419K1CvxnY6JhMk54Kzf5gtlGU</recordid><startdate>20080714</startdate><enddate>20080714</enddate><creator>Gaitanarou, Eleni</creator><creator>Seretis, Eleni</creator><creator>Xinopoulos, Dimitrios</creator><creator>Paraskevas, Emmanuel</creator><creator>Arnoyiannaki, Niki</creator><creator>Voloudakis-Baltatzis, Irene</creator><general>Department of Electron Microscopy-Cell Biology, "G. 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METHODS: Sixteen polyp tissues removed at colon- oscopy were examined. Tissues were investigated his- tologically and ultrastructurally. GST-pi expression was also analysed immunohistochemically, using peroxidase anti-peroxidase (PAP) method and immunogold label- ling method, for light and electron microscope respec- tively. RESULTS: All polyp tissues examined were adenoma of low, mild and high- grade dysplasia as shown in the histopathological reports. Nevertheless, the examina- tion of the above specimens with electron microscope revealed that 3 of 9 adenoma of mild dysplasia had ultrastuctural features similar to high-grade dysplasia adenoma. GST-pi was variably expressed in adenoma, with the lowest relative levels occurring in low-grade adenoma and the highest levels found in high-grade adenoma. GST-pi was located mainly in undifferentiat- ed epithelial cells. GST-pi positive particles were found in the cytoplasm and especially in the nucleus adjacent to the nuclear membrane of these cells. CONCLUSION: The overexpression of GST-pi in mild- grade adenomas with significant subcellular changes and in the majority of high-grade dysplasia adenoma suggests that this might be related to the carcinogenetic proceeding. Immunohistochemical localization of GST-pi in combination with ultrastructural changes indicate that GST-pi might be a sensitive agent for the detection of preneoplastic transformations in adenoma.</abstract><cop>United States</cop><pub>Department of Electron Microscopy-Cell Biology, "G. Papanicolaou" Research Center of Oncology and Experimental Surgery, "Agios Sawas" Anticancer Hospital of Athens, Athens 11522, Greece%Department of Gastroenterology, "Agios Savvas" Anticancer Hospital of Athens, Athens 11522, Greece%Department of Pathology of the Regional Anticancer-Oncologic Hospital of Athens "Agios Savvas", Athens 11522, Greece</pub><pmid>18636663</pmid><doi>10.3748/wjg.14.4179</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenoma - enzymology
Basic Research
Colonic Neoplasms - enzymology
Colonic Polyps - enzymology
Colonic Polyps - pathology
Colonic Polyps - ultrastructure
Glutathione S-Transferase pi - analysis
Humans
Immunohistochemistry
Microscopy, Electron
免疫组织化学
电子显微镜
结肠直肠息肉
title Immunohistochemical localization of glutathione S-transferase-pi in human colorectal polyps
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