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Frequent promoter methylation and gene silencing of CDH13 in pancreatic cancer
It has recently been reported that CDH13 expression is silenced by aberrant methylation of the promoter region in several cancers. We examined the methylation status of the CDH13 gene in pancreatic cancer using methylation‐specific PCR (MSP), and detected aberrant methylation of CDH13 in all 6 pancr...
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Published in: | Cancer science 2004-07, Vol.95 (7), p.588-591 |
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container_title | Cancer science |
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creator | Sakai, Mitsuru Hibi, Kenji Koshikawa, Katsumi Inoue, Soichiro Takeda, Shin Kaneko, Tetsuya Nakao, Akimasa |
description | It has recently been reported that CDH13 expression is silenced by aberrant methylation of the promoter region in several cancers. We examined the methylation status of the CDH13 gene in pancreatic cancer using methylation‐specific PCR (MSP), and detected aberrant methylation of CDH13 in all 6 pancreatic cancer cell lines examined. To confirm the status of the CDH13 gene in relation to the methylation pattern, we next examined CDH13 expression in these cell lines using reverse transcription (RT)‐PCR. As expected, no CDH13 expression was detected in any of the 6 pancreatic cancer cell lines. Moreover, 5‐aza‐2′‐deoxycytidine (5‐aza‐dC) treatment of CDH13‐methylated cell lines led to restoration of CDH13 expression. Among primary pancreatic cancers, 19 of 33 (58%) cases exhibited CDH13 methylation, while no cases exhibited it in corresponding normal pancreatic tissues. CDH13 methylation was detected even in relatively early pancreatic cancers, such as stage II cancers and cancers less than 2 cm in diameter. Our results suggest that the aberrant methylation of CDH13 occurs frequently in pancreatic cancer, even at a relatively early stage. |
doi_str_mv | 10.1111/j.1349-7006.2004.tb02491.x |
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We examined the methylation status of the CDH13 gene in pancreatic cancer using methylation‐specific PCR (MSP), and detected aberrant methylation of CDH13 in all 6 pancreatic cancer cell lines examined. To confirm the status of the CDH13 gene in relation to the methylation pattern, we next examined CDH13 expression in these cell lines using reverse transcription (RT)‐PCR. As expected, no CDH13 expression was detected in any of the 6 pancreatic cancer cell lines. Moreover, 5‐aza‐2′‐deoxycytidine (5‐aza‐dC) treatment of CDH13‐methylated cell lines led to restoration of CDH13 expression. Among primary pancreatic cancers, 19 of 33 (58%) cases exhibited CDH13 methylation, while no cases exhibited it in corresponding normal pancreatic tissues. CDH13 methylation was detected even in relatively early pancreatic cancers, such as stage II cancers and cancers less than 2 cm in diameter. Our results suggest that the aberrant methylation of CDH13 occurs frequently in pancreatic cancer, even at a relatively early stage.</description><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>DOI: 10.1111/j.1349-7006.2004.tb02491.x</identifier><identifier>PMID: 15245595</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Biological and medical sciences ; Cadherins - genetics ; Cadherins - metabolism ; Carcinogens ; DNA Methylation ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Gene Silencing ; Genes, Tumor Suppressor ; Humans ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Neoplasm Staging ; Pancreatic cancer ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - pathology ; Promoter Regions, Genetic ; Reverse Transcriptase Polymerase Chain Reaction ; Reverse transcription ; Tumor cell lines ; Tumor Cells, Cultured ; Tumors</subject><ispartof>Cancer science, 2004-07, Vol.95 (7), p.588-591</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright John Wiley & Sons, Inc. 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We examined the methylation status of the CDH13 gene in pancreatic cancer using methylation‐specific PCR (MSP), and detected aberrant methylation of CDH13 in all 6 pancreatic cancer cell lines examined. To confirm the status of the CDH13 gene in relation to the methylation pattern, we next examined CDH13 expression in these cell lines using reverse transcription (RT)‐PCR. As expected, no CDH13 expression was detected in any of the 6 pancreatic cancer cell lines. Moreover, 5‐aza‐2′‐deoxycytidine (5‐aza‐dC) treatment of CDH13‐methylated cell lines led to restoration of CDH13 expression. Among primary pancreatic cancers, 19 of 33 (58%) cases exhibited CDH13 methylation, while no cases exhibited it in corresponding normal pancreatic tissues. CDH13 methylation was detected even in relatively early pancreatic cancers, such as stage II cancers and cancers less than 2 cm in diameter. Our results suggest that the aberrant methylation of CDH13 occurs frequently in pancreatic cancer, even at a relatively early stage.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Cadherins - genetics</subject><subject>Cadherins - metabolism</subject><subject>Carcinogens</subject><subject>DNA Methylation</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gene Silencing</subject><subject>Genes, Tumor Suppressor</subject><subject>Humans</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Promoter Regions, Genetic</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Reverse transcription</subject><subject>Tumor cell lines</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><issn>1347-9032</issn><issn>1349-7006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqVkU1v1DAQhi0EomXhLyALBLcEfzvmAKoWSpEqOABny3GcrVeJvbWz0P33OGxUChfEXGakeebVzLwAPMOoxiVebWtMmaokQqImCLF6ahFhCtc398Dpbev-r1pWClFyAh7lvEWICqbYQ3CCOWGcK34KPp0nd713YYK7FMc4uQRHN10dBjP5GKAJHdy44GD2gwvWhw2MPVy_u8AU-gB3JtjkCmqhLaVLj8GD3gzZPVnyCnw7f_91fVFdfv7wcX12WVnRiKbqiG0473pbUsO4lbSjxirUSoW4o13bGuew7AvXckwsElxIS2QnbctUY-kKvD3q7vbt6DpbDkhm0LvkR5MOOhqv_-wEf6U38bsu_-MKYVwUXi4KKZYH5EmPPls3DCa4uM9aCKE4ZeKfIJZEKYJUAZ__BW7jPoXyBk2oUpJwVBRX4PWRsinmnFx_uzRG83ZYb_XsoZ491LO9erFX35Thp3fP_j26-FmAFwtgsjVDn4orPt_hlGw4m69_c-R-FF8P_7GCXp994U1DfwLYNcJM</recordid><startdate>200407</startdate><enddate>200407</enddate><creator>Sakai, Mitsuru</creator><creator>Hibi, Kenji</creator><creator>Koshikawa, Katsumi</creator><creator>Inoue, Soichiro</creator><creator>Takeda, Shin</creator><creator>Kaneko, Tetsuya</creator><creator>Nakao, Akimasa</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>John Wiley & Sons, Inc</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>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200407</creationdate><title>Frequent promoter methylation and gene silencing of CDH13 in pancreatic cancer</title><author>Sakai, Mitsuru ; Hibi, Kenji ; Koshikawa, Katsumi ; Inoue, Soichiro ; Takeda, Shin ; Kaneko, Tetsuya ; Nakao, Akimasa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6868-d2c855dfcc85845c73d3ac90b7905e3dbbaee17fd2cb512c06567c27d7cb498c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Cadherins - genetics</topic><topic>Cadherins - metabolism</topic><topic>Carcinogens</topic><topic>DNA Methylation</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gene Silencing</topic><topic>Genes, Tumor Suppressor</topic><topic>Humans</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms - genetics</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Promoter Regions, Genetic</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Reverse transcription</topic><topic>Tumor cell lines</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakai, Mitsuru</creatorcontrib><creatorcontrib>Hibi, Kenji</creatorcontrib><creatorcontrib>Koshikawa, Katsumi</creatorcontrib><creatorcontrib>Inoue, Soichiro</creatorcontrib><creatorcontrib>Takeda, Shin</creatorcontrib><creatorcontrib>Kaneko, Tetsuya</creatorcontrib><creatorcontrib>Nakao, Akimasa</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 SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Sakai, Mitsuru</au><au>Hibi, Kenji</au><au>Koshikawa, Katsumi</au><au>Inoue, Soichiro</au><au>Takeda, Shin</au><au>Kaneko, Tetsuya</au><au>Nakao, Akimasa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frequent promoter methylation and gene silencing of CDH13 in pancreatic cancer</atitle><jtitle>Cancer science</jtitle><addtitle>Cancer Sci</addtitle><date>2004-07</date><risdate>2004</risdate><volume>95</volume><issue>7</issue><spage>588</spage><epage>591</epage><pages>588-591</pages><issn>1347-9032</issn><eissn>1349-7006</eissn><abstract>It has recently been reported that CDH13 expression is silenced by aberrant methylation of the promoter region in several cancers. We examined the methylation status of the CDH13 gene in pancreatic cancer using methylation‐specific PCR (MSP), and detected aberrant methylation of CDH13 in all 6 pancreatic cancer cell lines examined. To confirm the status of the CDH13 gene in relation to the methylation pattern, we next examined CDH13 expression in these cell lines using reverse transcription (RT)‐PCR. As expected, no CDH13 expression was detected in any of the 6 pancreatic cancer cell lines. Moreover, 5‐aza‐2′‐deoxycytidine (5‐aza‐dC) treatment of CDH13‐methylated cell lines led to restoration of CDH13 expression. Among primary pancreatic cancers, 19 of 33 (58%) cases exhibited CDH13 methylation, while no cases exhibited it in corresponding normal pancreatic tissues. CDH13 methylation was detected even in relatively early pancreatic cancers, such as stage II cancers and cancers less than 2 cm in diameter. Our results suggest that the aberrant methylation of CDH13 occurs frequently in pancreatic cancer, even at a relatively early stage.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>15245595</pmid><doi>10.1111/j.1349-7006.2004.tb02491.x</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Biological and medical sciences Cadherins - genetics Cadherins - metabolism Carcinogens DNA Methylation Female Gastroenterology. Liver. Pancreas. Abdomen Gene Silencing Genes, Tumor Suppressor Humans Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Neoplasm Staging Pancreatic cancer Pancreatic Neoplasms - genetics Pancreatic Neoplasms - pathology Promoter Regions, Genetic Reverse Transcriptase Polymerase Chain Reaction Reverse transcription Tumor cell lines Tumor Cells, Cultured Tumors |
title | Frequent promoter methylation and gene silencing of CDH13 in pancreatic cancer |
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