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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c4555-ce43e7b9eba8cdc0ad5cf766342a7a8489b3752b3f11b9cdb3af5d8b208bdeec3
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container_issue 9
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container_title International journal of cancer
container_volume 127
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). 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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). 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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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