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Characteristic methylation profile in CpG island methylator phenotype‐negative distal colorectal cancers
Aberrant DNA methylation is involved in colon carcinogenesis. Although the CpG island methylator phenotype (CIMP) is defined as a subset of colorectal cancers (CRCs) with remarkably high levels of DNA methylation, it is not known whether epigenetic processes are also involved in CIMP‐negative tumors...
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Published in: | International journal of cancer 2010-11, Vol.127 (9), p.2095-2105 |
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creator | An, Byonggu Kondo, Yutaka Okamoto, Yasuyuki Shinjo, Keiko Kanemitsu, Yukihide Komori, Koji Hirai, Takashi Sawaki, Akira Tajika, Masahiro Nakamura, Tsuneya Yamao, Kenji Yatabe, Yasushi Fujii, Makiko Murakami, Hideki Osada, Hirotaka Tani, Tohru Matsuo, Keitaro Shen, Lanlan Issa, Jean‐Pierre J. Sekido, Yoshitaka |
description | Aberrant DNA methylation is involved in colon carcinogenesis. Although the CpG island methylator phenotype (CIMP) is defined as a subset of colorectal cancers (CRCs) with remarkably high levels of DNA methylation, it is not known whether epigenetic processes are also involved in CIMP‐negative tumors. We analyzed the DNA methylation profiles of 94 CRCs and their corresponding normal‐appearing colonic mucosa with 11 different markers, including the five classical CIMP markers. The CIMP markers were frequently methylated in proximal CRCs (p < 0.01); however, RASSF1A methylation levels were significantly higher in distal CRCs, the majority of which are CIMP‐negative (p < 0.05). Similarly, methylation levels of RASSF1A and SFRP1 in the normal‐appearing mucosae of distal CRC cases were significantly higher than those in the proximal CRC cases (p < 0.05). They were also positively correlated with age (RASSF1A, p < 0.01; SFRP1, p < 0.01). Microarray‐based genome‐wide DNA methylation analysis of 18 CRCs revealed that 168 genes and 720 genes were preferentially methylated in CIMP‐negative distal CRCs and CIMP‐positive CRCs, respectively. Interestingly, more than half of the hypermethylated genes in CIMP‐negative distal CRCs were also methylated in the normal‐appearing mucosae, indicating that hypermethylation in CIMP‐negative distal CRCs is more closely associated with age‐related methylation. By contrast, more than 60% of the hypermethylated genes in CIMP‐positive proximal CRCs were cancer specific (p < 0.01). These data altogether suggest that CpG island promoters appear to be methylated in different ways depending on location, a finding which may imply the presence of different mechanisms for the acquisition of epigenetic changes during colon tumorigenesis. |
doi_str_mv | 10.1002/ijc.25225 |
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Although the CpG island methylator phenotype (CIMP) is defined as a subset of colorectal cancers (CRCs) with remarkably high levels of DNA methylation, it is not known whether epigenetic processes are also involved in CIMP‐negative tumors. We analyzed the DNA methylation profiles of 94 CRCs and their corresponding normal‐appearing colonic mucosa with 11 different markers, including the five classical CIMP markers. The CIMP markers were frequently methylated in proximal CRCs (p < 0.01); however, RASSF1A methylation levels were significantly higher in distal CRCs, the majority of which are CIMP‐negative (p < 0.05). Similarly, methylation levels of RASSF1A and SFRP1 in the normal‐appearing mucosae of distal CRC cases were significantly higher than those in the proximal CRC cases (p < 0.05). They were also positively correlated with age (RASSF1A, p < 0.01; SFRP1, p < 0.01). Microarray‐based genome‐wide DNA methylation analysis of 18 CRCs revealed that 168 genes and 720 genes were preferentially methylated in CIMP‐negative distal CRCs and CIMP‐positive CRCs, respectively. Interestingly, more than half of the hypermethylated genes in CIMP‐negative distal CRCs were also methylated in the normal‐appearing mucosae, indicating that hypermethylation in CIMP‐negative distal CRCs is more closely associated with age‐related methylation. By contrast, more than 60% of the hypermethylated genes in CIMP‐positive proximal CRCs were cancer specific (p < 0.01). These data altogether suggest that CpG island promoters appear to be methylated in different ways depending on location, a finding which may imply the presence of different mechanisms for the acquisition of epigenetic changes during colon tumorigenesis.]]></description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.25225</identifier><identifier>PMID: 20131317</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Age Factors ; Aged ; Aged, 80 and over ; Biological and medical sciences ; colon cancer ; Colorectal Neoplasms - chemically induced ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - pathology ; CpG Islands ; DNA Methylation ; Female ; field defect ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Intestinal Mucosa - metabolism ; Long Interspersed Nucleotide Elements ; Male ; Medical sciences ; microarray ; Middle Aged ; Phenotype ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>International journal of cancer, 2010-11, Vol.127 (9), p.2095-2105</ispartof><rights>Copyright © 2010 UICC</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4555-ce43e7b9eba8cdc0ad5cf766342a7a8489b3752b3f11b9cdb3af5d8b208bdeec3</citedby><cites>FETCH-LOGICAL-c4555-ce43e7b9eba8cdc0ad5cf766342a7a8489b3752b3f11b9cdb3af5d8b208bdeec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23253310$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20131317$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>An, Byonggu</creatorcontrib><creatorcontrib>Kondo, Yutaka</creatorcontrib><creatorcontrib>Okamoto, Yasuyuki</creatorcontrib><creatorcontrib>Shinjo, Keiko</creatorcontrib><creatorcontrib>Kanemitsu, Yukihide</creatorcontrib><creatorcontrib>Komori, Koji</creatorcontrib><creatorcontrib>Hirai, Takashi</creatorcontrib><creatorcontrib>Sawaki, Akira</creatorcontrib><creatorcontrib>Tajika, Masahiro</creatorcontrib><creatorcontrib>Nakamura, Tsuneya</creatorcontrib><creatorcontrib>Yamao, Kenji</creatorcontrib><creatorcontrib>Yatabe, Yasushi</creatorcontrib><creatorcontrib>Fujii, Makiko</creatorcontrib><creatorcontrib>Murakami, Hideki</creatorcontrib><creatorcontrib>Osada, Hirotaka</creatorcontrib><creatorcontrib>Tani, Tohru</creatorcontrib><creatorcontrib>Matsuo, Keitaro</creatorcontrib><creatorcontrib>Shen, Lanlan</creatorcontrib><creatorcontrib>Issa, Jean‐Pierre J.</creatorcontrib><creatorcontrib>Sekido, Yoshitaka</creatorcontrib><title>Characteristic methylation profile in CpG island methylator phenotype‐negative distal colorectal cancers</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description><![CDATA[Aberrant DNA methylation is involved in colon carcinogenesis. Although the CpG island methylator phenotype (CIMP) is defined as a subset of colorectal cancers (CRCs) with remarkably high levels of DNA methylation, it is not known whether epigenetic processes are also involved in CIMP‐negative tumors. We analyzed the DNA methylation profiles of 94 CRCs and their corresponding normal‐appearing colonic mucosa with 11 different markers, including the five classical CIMP markers. The CIMP markers were frequently methylated in proximal CRCs (p < 0.01); however, RASSF1A methylation levels were significantly higher in distal CRCs, the majority of which are CIMP‐negative (p < 0.05). Similarly, methylation levels of RASSF1A and SFRP1 in the normal‐appearing mucosae of distal CRC cases were significantly higher than those in the proximal CRC cases (p < 0.05). They were also positively correlated with age (RASSF1A, p < 0.01; SFRP1, p < 0.01). Microarray‐based genome‐wide DNA methylation analysis of 18 CRCs revealed that 168 genes and 720 genes were preferentially methylated in CIMP‐negative distal CRCs and CIMP‐positive CRCs, respectively. Interestingly, more than half of the hypermethylated genes in CIMP‐negative distal CRCs were also methylated in the normal‐appearing mucosae, indicating that hypermethylation in CIMP‐negative distal CRCs is more closely associated with age‐related methylation. By contrast, more than 60% of the hypermethylated genes in CIMP‐positive proximal CRCs were cancer specific (p < 0.01). These data altogether suggest that CpG island promoters appear to be methylated in different ways depending on location, a finding which may imply the presence of different mechanisms for the acquisition of epigenetic changes during colon tumorigenesis.]]></description><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>colon cancer</subject><subject>Colorectal Neoplasms - chemically induced</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - pathology</subject><subject>CpG Islands</subject><subject>DNA Methylation</subject><subject>Female</subject><subject>field defect</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Long Interspersed Nucleotide Elements</subject><subject>Male</subject><subject>Medical sciences</subject><subject>microarray</subject><subject>Middle Aged</subject><subject>Phenotype</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp1kLtOwzAUhi0EouUy8ALICwNDWl_iJhlRBKWoEgvMkS8n1FWaRHYAZeMReEaeBNOUMqEz-Ej-_P_yh9AFJRNKCJvatZ4wwZg4QGNKsiQijIpDNA53JEoon43QifdrQigVJD5GI0YoD5OM0TpfSSd1B876zmq8gW7VV7KzTY1b15S2AmxrnLdzbH0la7MnGofbFdRN17fw9fFZw0t49QbYhCBZYd1UjQO9XWWtwfkzdFTKysP57jxFz3e3T_l9tHycL_KbZaRjIUSkIeaQqAyUTLXRRBqhy2Q24zGTiUzjNFM8EUzxklKVaaO4LIVJFSOpMgCan6LrIVe7xnsHZdE6u5GuLygpfnwVwVex9RXYy4FtX9UGzJ78FRSAqx0gvZZV6cJfrP_jeAjhlARuOnDvwVj_f2OxeMiH6m9IXIXE</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>An, Byonggu</creator><creator>Kondo, Yutaka</creator><creator>Okamoto, Yasuyuki</creator><creator>Shinjo, Keiko</creator><creator>Kanemitsu, Yukihide</creator><creator>Komori, Koji</creator><creator>Hirai, Takashi</creator><creator>Sawaki, Akira</creator><creator>Tajika, Masahiro</creator><creator>Nakamura, Tsuneya</creator><creator>Yamao, Kenji</creator><creator>Yatabe, Yasushi</creator><creator>Fujii, Makiko</creator><creator>Murakami, Hideki</creator><creator>Osada, Hirotaka</creator><creator>Tani, Tohru</creator><creator>Matsuo, Keitaro</creator><creator>Shen, Lanlan</creator><creator>Issa, Jean‐Pierre J.</creator><creator>Sekido, Yoshitaka</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</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></search><sort><creationdate>20101101</creationdate><title>Characteristic methylation profile in CpG island methylator phenotype‐negative distal colorectal cancers</title><author>An, Byonggu ; Kondo, Yutaka ; Okamoto, Yasuyuki ; Shinjo, Keiko ; Kanemitsu, Yukihide ; Komori, Koji ; Hirai, Takashi ; Sawaki, Akira ; Tajika, Masahiro ; Nakamura, Tsuneya ; Yamao, Kenji ; Yatabe, Yasushi ; Fujii, Makiko ; Murakami, Hideki ; Osada, Hirotaka ; Tani, Tohru ; Matsuo, Keitaro ; Shen, Lanlan ; Issa, Jean‐Pierre J. ; Sekido, Yoshitaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4555-ce43e7b9eba8cdc0ad5cf766342a7a8489b3752b3f11b9cdb3af5d8b208bdeec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>colon cancer</topic><topic>Colorectal Neoplasms - chemically induced</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - pathology</topic><topic>CpG Islands</topic><topic>DNA Methylation</topic><topic>Female</topic><topic>field defect</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Long Interspersed Nucleotide Elements</topic><topic>Male</topic><topic>Medical sciences</topic><topic>microarray</topic><topic>Middle Aged</topic><topic>Phenotype</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>An, Byonggu</creatorcontrib><creatorcontrib>Kondo, Yutaka</creatorcontrib><creatorcontrib>Okamoto, Yasuyuki</creatorcontrib><creatorcontrib>Shinjo, Keiko</creatorcontrib><creatorcontrib>Kanemitsu, Yukihide</creatorcontrib><creatorcontrib>Komori, Koji</creatorcontrib><creatorcontrib>Hirai, Takashi</creatorcontrib><creatorcontrib>Sawaki, Akira</creatorcontrib><creatorcontrib>Tajika, Masahiro</creatorcontrib><creatorcontrib>Nakamura, Tsuneya</creatorcontrib><creatorcontrib>Yamao, Kenji</creatorcontrib><creatorcontrib>Yatabe, Yasushi</creatorcontrib><creatorcontrib>Fujii, Makiko</creatorcontrib><creatorcontrib>Murakami, Hideki</creatorcontrib><creatorcontrib>Osada, Hirotaka</creatorcontrib><creatorcontrib>Tani, Tohru</creatorcontrib><creatorcontrib>Matsuo, Keitaro</creatorcontrib><creatorcontrib>Shen, Lanlan</creatorcontrib><creatorcontrib>Issa, Jean‐Pierre J.</creatorcontrib><creatorcontrib>Sekido, Yoshitaka</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><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>An, Byonggu</au><au>Kondo, Yutaka</au><au>Okamoto, Yasuyuki</au><au>Shinjo, Keiko</au><au>Kanemitsu, Yukihide</au><au>Komori, Koji</au><au>Hirai, Takashi</au><au>Sawaki, Akira</au><au>Tajika, Masahiro</au><au>Nakamura, Tsuneya</au><au>Yamao, Kenji</au><au>Yatabe, Yasushi</au><au>Fujii, Makiko</au><au>Murakami, Hideki</au><au>Osada, Hirotaka</au><au>Tani, Tohru</au><au>Matsuo, Keitaro</au><au>Shen, Lanlan</au><au>Issa, Jean‐Pierre J.</au><au>Sekido, Yoshitaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characteristic methylation profile in CpG island methylator phenotype‐negative distal colorectal cancers</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>127</volume><issue>9</issue><spage>2095</spage><epage>2105</epage><pages>2095-2105</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract><![CDATA[Aberrant DNA methylation is involved in colon carcinogenesis. Although the CpG island methylator phenotype (CIMP) is defined as a subset of colorectal cancers (CRCs) with remarkably high levels of DNA methylation, it is not known whether epigenetic processes are also involved in CIMP‐negative tumors. We analyzed the DNA methylation profiles of 94 CRCs and their corresponding normal‐appearing colonic mucosa with 11 different markers, including the five classical CIMP markers. The CIMP markers were frequently methylated in proximal CRCs (p < 0.01); however, RASSF1A methylation levels were significantly higher in distal CRCs, the majority of which are CIMP‐negative (p < 0.05). Similarly, methylation levels of RASSF1A and SFRP1 in the normal‐appearing mucosae of distal CRC cases were significantly higher than those in the proximal CRC cases (p < 0.05). They were also positively correlated with age (RASSF1A, p < 0.01; SFRP1, p < 0.01). Microarray‐based genome‐wide DNA methylation analysis of 18 CRCs revealed that 168 genes and 720 genes were preferentially methylated in CIMP‐negative distal CRCs and CIMP‐positive CRCs, respectively. Interestingly, more than half of the hypermethylated genes in CIMP‐negative distal CRCs were also methylated in the normal‐appearing mucosae, indicating that hypermethylation in CIMP‐negative distal CRCs is more closely associated with age‐related methylation. By contrast, more than 60% of the hypermethylated genes in CIMP‐positive proximal CRCs were cancer specific (p < 0.01). These data altogether suggest that CpG island promoters appear to be methylated in different ways depending on location, a finding which may imply the presence of different mechanisms for the acquisition of epigenetic changes during colon tumorigenesis.]]></abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20131317</pmid><doi>10.1002/ijc.25225</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Age Factors Aged Aged, 80 and over Biological and medical sciences colon cancer Colorectal Neoplasms - chemically induced Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology CpG Islands DNA Methylation Female field defect Gastroenterology. Liver. Pancreas. Abdomen Humans Intestinal Mucosa - metabolism Long Interspersed Nucleotide Elements Male Medical sciences microarray Middle Aged Phenotype Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Characteristic methylation profile in CpG island methylator phenotype‐negative distal colorectal cancers |
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