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BRAF mutation, CpG island methylator phenotype and microsatellite instability occur more frequently and concordantly in mucinous than non‐mucinous colorectal cancer
Author(s) -
Tanaka Hirofumi,
Deng Guoren,
Matsuzaki Koji,
Kakar Sanjay,
Kim Grace E.,
Miura Soichiro,
Sleisenger Marvin H.,
Kim Young S.
Publication year - 2006
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.21701
Subject(s) - kras , microsatellite instability , colorectal cancer , biology , mutation , cancer research , adenocarcinoma , mlh1 , cancer , medicine , oncology , dna mismatch repair , genetics , microsatellite , allele , gene
Mucinous colorectal cancer (CRC) has been reported to have distinct clinicopathological and genetic characteristics. However, the incidence and the relationship among microsatellite instability (MSI), CpG island methylator phenotype (CIMP) and BRAF and KRAS mutations in mucinous and non‐mucinous CRC are not known. Activating mutations of BRAF and KRAS and their relationship with MSI and CIMP were examined in 83 sporadic CRC specimens (26 mucinous and 57 non‐mucinous CRC). MSI, CIMP, BRAF and KRAS mutation were observed in 17, 24, 25 and 36% of the tumors, respectively. BRAF mutation was highly correlated with MSI ( p < 0.001) and CIMP ( p < 0.001). A higher incidence of MSI (27% vs . 12%), CIMP (38% vs . 18%, p < 0.05) and BRAF mutation (46% vs . 16%, p < 0.01) was observed in mucinous CRC. KRAS mutation (27% vs . 40%) was observed more frequently in non‐mucinous CRC. Significantly higher percentages of mucinous CRC (54%, p < 0.05) had MSI or CIMP or BRAF mutations. Concordant occurrence of 2 or more of these alterations was observed in 39% of mucinous CRC and only 11% of non‐mucinous CRC ( p < 0.01). The more frequent occurrence and closer association among MSI, CIMP and BRAF mutation in mucinous CRC observed in our study further supports the idea that its pathogenesis may involve distinct genetic and epigenetic changes. © 2005 Wiley‐Liss, Inc.