Item type |
学内発行雑誌 / Departmental Bulletin Paper(1) |
公開日 |
2016-11-18 |
タイトル |
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タイトル |
CpG Island Methylator Phenotype in Primary Gastric Carcinoma |
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言語 |
en |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ |
departmental bulletin paper |
著者 |
TOJO, Masayuki
KONISHI, Kazuo
YANO, Yuichiro
KATAGIRI, Atsushi
NOZAWA, Hisako
KUBOTA, Yutaro
MURAMOTO, Takashi
KONDA, Kenichi
SHINMURA, Kensuke
TAKIMOTO, Masafumi
IMAWARI, Michio
YOSHIDA, Hitoshi
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書誌情報 |
The Showa University journal of medical sciences
巻 25,
号 2,
p. 127-132,
発行日 2013-06
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抄録 |
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内容記述タイプ |
Abstract |
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内容記述 |
Gastric cancers (GC) with methylation of multiple CpG islands have a CpG island methylator phenotype (CIMP) and they can have different biological features. The aim of this study was to investigate the DNA methylation status of GCs and its association with their clinicopathological features. We evaluated the methylation status of four genes (MINT1, MINT2, MINT25 and MINT31) in 105 primary GCs using bisulfite-pyrosequencing analysis. We classified tumors as CIMP-high (CIMP-H), CIMP-low (CIMP-L) or CIMP-negative (CIMP-N) based on the methylation of MINT1, MINT2, MINT25, and MINT31. Overall, the prevalence of CIMP-H, CIMP-L and CIMP-N was 22% (23/105), 52% (55/105) and 26% (27/105), respectively. We observed a significant difference in tumor stage (stages I-II vs. stages III-IV) between CIMP-H and CIMP-N tumors (P = 0.0435). No significant differences were observed in clinicopathological characteristics (gender, age, location and tumor differentiation) among the CIMP phenotypes. The prognoses of patients with a CIMP-H tumor is likely to be better than those with CIMP-L or CIMP-N tumors, but these differences are not statistically significant (P = 0.074 and P = 0.200). Our results suggest that CIMP may define a subgroup of GCs with distinct biological features. |
DOI |
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関連タイプ |
isIdenticalTo |
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関連識別子 |
10.15369/sujms.25.127 |
出版者 |
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出版者 |
Showa University Society |
ISSN |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
0915-6380 |
出版タイプ |
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出版タイプ |
VoR |