Overexpression of Human X-box Binding Protein 1 (XBP-1) in Colorectal Adenomas and Adenocarcinomas
Background: Human X-box binding protein 1 (XBP-1) is a transcription factor essential for hepatocyte growth, as well as for plasma cell differentiation. Recently, overexpression of XBP-1 has been reported in breast cancer including non-invasive carcinomas, and was suggested to play an important role...
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creator | FUJIMOTO, Takashi YOSHIMATSU, Kazuhiko WATANABE, Kiyo YOKOMIZO, Hajime OTANI, Taisuke MATSUMOTO, Atsuo OSAWA, Gakuji ONDA, Masamitsu OGAWA, Kenji |
description | Background: Human X-box binding protein 1 (XBP-1) is a transcription factor essential for hepatocyte growth, as well as for
plasma cell differentiation. Recently, overexpression of XBP-1 has been reported in breast cancer including non-invasive carcinomas,
and was suggested to play an important role in breast carcinogenesis. To investigate the involvement of XBP-1 in colorectal
tumorigenecity, the expression of XBP-1 was examined in four colon cancer cell lines, six colorectal polyps and five colorectal
carcinomas. Materials and Methods: The study population consisted of eleven patients who had undergone resection for colorectal
cancer or adenoma from 2000 to 2002. Four colon cancer cell lines, DLD1, SW480, HCT15 and WiDr, were also analyzed for expression
of XBP-1. Reverse transcription-polymerase chain reaction was performed using eleven primary colon tumors. XBP-1 expression
was then investigated using an immunohistochemical method for archived paraffin-embedded sections. Results: The XBP-1 gene
was overexpressed in four cases out of five primary colorectal carcinomas and in four cases out of six colorectal adenomas.
Also all four cancer cell lines expressed XBP-1 mRNA. Immunohistochemical staining demonstrated that XBP-1 protein was strongly
stained in the cytoplasms of cancer cells, whereas it was unreactive in the normal colon epithelial cells and stromal cells.
Conclusion: These data indicate that increased expression of XBP-1 gene may play some role in human colon carcinogenesis through
impairment of cell differentiation regulation. |
format | Article |
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plasma cell differentiation. Recently, overexpression of XBP-1 has been reported in breast cancer including non-invasive carcinomas,
and was suggested to play an important role in breast carcinogenesis. To investigate the involvement of XBP-1 in colorectal
tumorigenecity, the expression of XBP-1 was examined in four colon cancer cell lines, six colorectal polyps and five colorectal
carcinomas. Materials and Methods: The study population consisted of eleven patients who had undergone resection for colorectal
cancer or adenoma from 2000 to 2002. Four colon cancer cell lines, DLD1, SW480, HCT15 and WiDr, were also analyzed for expression
of XBP-1. Reverse transcription-polymerase chain reaction was performed using eleven primary colon tumors. XBP-1 expression
was then investigated using an immunohistochemical method for archived paraffin-embedded sections. Results: The XBP-1 gene
was overexpressed in four cases out of five primary colorectal carcinomas and in four cases out of six colorectal adenomas.
Also all four cancer cell lines expressed XBP-1 mRNA. Immunohistochemical staining demonstrated that XBP-1 protein was strongly
stained in the cytoplasms of cancer cells, whereas it was unreactive in the normal colon epithelial cells and stromal cells.
Conclusion: These data indicate that increased expression of XBP-1 gene may play some role in human colon carcinogenesis through
impairment of cell differentiation regulation.</description><identifier>ISSN: 0250-7005</identifier><identifier>EISSN: 1791-7530</identifier><identifier>PMID: 17352224</identifier><language>eng</language><publisher>Attiki: International Institute of Anticancer Research</publisher><subject>Adenocarcinoma - genetics ; Adenocarcinoma - metabolism ; Adenoma - genetics ; Adenoma - metabolism ; Aged ; Biological and medical sciences ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - metabolism ; DNA-Binding Proteins - biosynthesis ; DNA-Binding Proteins - genetics ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Immunohistochemistry ; Male ; Medical sciences ; Middle Aged ; Nuclear Proteins - biosynthesis ; Nuclear Proteins - genetics ; Regulatory Factor X Transcription Factors ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - biosynthesis ; RNA, Messenger - genetics ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Transcription Factors ; Tumors ; X-Box Binding Protein 1</subject><ispartof>Anticancer research, 2007-01, Vol.27 (1A), p.127-131</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18562363$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17352224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FUJIMOTO, Takashi</creatorcontrib><creatorcontrib>YOSHIMATSU, Kazuhiko</creatorcontrib><creatorcontrib>WATANABE, Kiyo</creatorcontrib><creatorcontrib>YOKOMIZO, Hajime</creatorcontrib><creatorcontrib>OTANI, Taisuke</creatorcontrib><creatorcontrib>MATSUMOTO, Atsuo</creatorcontrib><creatorcontrib>OSAWA, Gakuji</creatorcontrib><creatorcontrib>ONDA, Masamitsu</creatorcontrib><creatorcontrib>OGAWA, Kenji</creatorcontrib><title>Overexpression of Human X-box Binding Protein 1 (XBP-1) in Colorectal Adenomas and Adenocarcinomas</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><description>Background: Human X-box binding protein 1 (XBP-1) is a transcription factor essential for hepatocyte growth, as well as for
plasma cell differentiation. Recently, overexpression of XBP-1 has been reported in breast cancer including non-invasive carcinomas,
and was suggested to play an important role in breast carcinogenesis. To investigate the involvement of XBP-1 in colorectal
tumorigenecity, the expression of XBP-1 was examined in four colon cancer cell lines, six colorectal polyps and five colorectal
carcinomas. Materials and Methods: The study population consisted of eleven patients who had undergone resection for colorectal
cancer or adenoma from 2000 to 2002. Four colon cancer cell lines, DLD1, SW480, HCT15 and WiDr, were also analyzed for expression
of XBP-1. Reverse transcription-polymerase chain reaction was performed using eleven primary colon tumors. XBP-1 expression
was then investigated using an immunohistochemical method for archived paraffin-embedded sections. Results: The XBP-1 gene
was overexpressed in four cases out of five primary colorectal carcinomas and in four cases out of six colorectal adenomas.
Also all four cancer cell lines expressed XBP-1 mRNA. Immunohistochemical staining demonstrated that XBP-1 protein was strongly
stained in the cytoplasms of cancer cells, whereas it was unreactive in the normal colon epithelial cells and stromal cells.
Conclusion: These data indicate that increased expression of XBP-1 gene may play some role in human colon carcinogenesis through
impairment of cell differentiation regulation.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - metabolism</subject><subject>Adenoma - genetics</subject><subject>Adenoma - metabolism</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>DNA-Binding Proteins - biosynthesis</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nuclear Proteins - biosynthesis</subject><subject>Nuclear Proteins - genetics</subject><subject>Regulatory Factor X Transcription Factors</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RNA, Messenger - genetics</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Transcription Factors</subject><subject>Tumors</subject><subject>X-Box Binding Protein 1</subject><issn>0250-7005</issn><issn>1791-7530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFj8tKAzEARYModqz-gmQj6CKQx2QyWbZFrVBoFwrdDXlNG5lJStJq_XuLrXR1OZfDhXsBCiIkQYIzfAkKTDlGAmM-ADc5f2JcVbJm12BABOOU0rIAev7lkttvksvZxwBjC6e7XgW4RDru4dgH68MKLlLcOh8ggY_L8QKRJ3iASexicmarOjiyLsReZaiCPYJRyfi_7hZctarL7u6UQ_Dx8vw-maLZ_PVtMpqhNa3kFrWctS0pnTRaU6I5qbnBkmtqhCudU8baujac6Npai3FppJWCllaVsjLMWTYE98fdzU73zjab5HuVfpr_swfh4SSobFTXJhWMz2ev5hVlFTt7a79af_vkmtyrrjvMskYlKhoyaggV7BejI2tH</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>FUJIMOTO, Takashi</creator><creator>YOSHIMATSU, Kazuhiko</creator><creator>WATANABE, Kiyo</creator><creator>YOKOMIZO, Hajime</creator><creator>OTANI, Taisuke</creator><creator>MATSUMOTO, Atsuo</creator><creator>OSAWA, Gakuji</creator><creator>ONDA, Masamitsu</creator><creator>OGAWA, Kenji</creator><general>International Institute of Anticancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20070101</creationdate><title>Overexpression of Human X-box Binding Protein 1 (XBP-1) in Colorectal Adenomas and Adenocarcinomas</title><author>FUJIMOTO, Takashi ; YOSHIMATSU, Kazuhiko ; WATANABE, Kiyo ; YOKOMIZO, Hajime ; OTANI, Taisuke ; MATSUMOTO, Atsuo ; OSAWA, Gakuji ; ONDA, Masamitsu ; OGAWA, Kenji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h269t-f53ff14e9cbb21b5185c095b2c7e4eeacdd88c51b8ddd004c9d9724da496c3ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - metabolism</topic><topic>Adenoma - genetics</topic><topic>Adenoma - metabolism</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>DNA-Binding Proteins - biosynthesis</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nuclear Proteins - biosynthesis</topic><topic>Nuclear Proteins - genetics</topic><topic>Regulatory Factor X Transcription Factors</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Transcription Factors</topic><topic>Tumors</topic><topic>X-Box Binding Protein 1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FUJIMOTO, Takashi</creatorcontrib><creatorcontrib>YOSHIMATSU, Kazuhiko</creatorcontrib><creatorcontrib>WATANABE, Kiyo</creatorcontrib><creatorcontrib>YOKOMIZO, Hajime</creatorcontrib><creatorcontrib>OTANI, Taisuke</creatorcontrib><creatorcontrib>MATSUMOTO, Atsuo</creatorcontrib><creatorcontrib>OSAWA, Gakuji</creatorcontrib><creatorcontrib>ONDA, Masamitsu</creatorcontrib><creatorcontrib>OGAWA, Kenji</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Anticancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FUJIMOTO, Takashi</au><au>YOSHIMATSU, Kazuhiko</au><au>WATANABE, Kiyo</au><au>YOKOMIZO, Hajime</au><au>OTANI, Taisuke</au><au>MATSUMOTO, Atsuo</au><au>OSAWA, Gakuji</au><au>ONDA, Masamitsu</au><au>OGAWA, Kenji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of Human X-box Binding Protein 1 (XBP-1) in Colorectal Adenomas and Adenocarcinomas</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2007-01-01</date><risdate>2007</risdate><volume>27</volume><issue>1A</issue><spage>127</spage><epage>131</epage><pages>127-131</pages><issn>0250-7005</issn><eissn>1791-7530</eissn><abstract>Background: Human X-box binding protein 1 (XBP-1) is a transcription factor essential for hepatocyte growth, as well as for
plasma cell differentiation. Recently, overexpression of XBP-1 has been reported in breast cancer including non-invasive carcinomas,
and was suggested to play an important role in breast carcinogenesis. To investigate the involvement of XBP-1 in colorectal
tumorigenecity, the expression of XBP-1 was examined in four colon cancer cell lines, six colorectal polyps and five colorectal
carcinomas. Materials and Methods: The study population consisted of eleven patients who had undergone resection for colorectal
cancer or adenoma from 2000 to 2002. Four colon cancer cell lines, DLD1, SW480, HCT15 and WiDr, were also analyzed for expression
of XBP-1. Reverse transcription-polymerase chain reaction was performed using eleven primary colon tumors. XBP-1 expression
was then investigated using an immunohistochemical method for archived paraffin-embedded sections. Results: The XBP-1 gene
was overexpressed in four cases out of five primary colorectal carcinomas and in four cases out of six colorectal adenomas.
Also all four cancer cell lines expressed XBP-1 mRNA. Immunohistochemical staining demonstrated that XBP-1 protein was strongly
stained in the cytoplasms of cancer cells, whereas it was unreactive in the normal colon epithelial cells and stromal cells.
Conclusion: These data indicate that increased expression of XBP-1 gene may play some role in human colon carcinogenesis through
impairment of cell differentiation regulation.</abstract><cop>Attiki</cop><pub>International Institute of Anticancer Research</pub><pmid>17352224</pmid><tpages>5</tpages></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Adenocarcinoma - genetics Adenocarcinoma - metabolism Adenoma - genetics Adenoma - metabolism Aged Biological and medical sciences Colorectal Neoplasms - genetics Colorectal Neoplasms - metabolism DNA-Binding Proteins - biosynthesis DNA-Binding Proteins - genetics Female Gastroenterology. Liver. Pancreas. Abdomen Humans Immunohistochemistry Male Medical sciences Middle Aged Nuclear Proteins - biosynthesis Nuclear Proteins - genetics Regulatory Factor X Transcription Factors Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - biosynthesis RNA, Messenger - genetics Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Transcription Factors Tumors X-Box Binding Protein 1 |
title | Overexpression of Human X-box Binding Protein 1 (XBP-1) in Colorectal Adenomas and Adenocarcinomas |
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