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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Veröffentlicht in:Anticancer research 2007-01, Vol.27 (1A), p.127-131
Hauptverfasser: FUJIMOTO, Takashi, YOSHIMATSU, Kazuhiko, WATANABE, Kiyo, YOKOMIZO, Hajime, OTANI, Taisuke, MATSUMOTO, Atsuo, OSAWA, Gakuji, ONDA, Masamitsu, OGAWA, Kenji
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container_end_page 131
container_issue 1A
container_start_page 127
container_title Anticancer research
container_volume 27
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.
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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. 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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. 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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. 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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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