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  1. 学内発行雑誌
  2. The Showa University journal of medical sciences
  3. Vol.25(2013)
  4. No.2

CpG Island Methylator Phenotype in Primary Gastric Carcinoma

https://showa.repo.nii.ac.jp/records/650
https://showa.repo.nii.ac.jp/records/650
283064b8-1706-407b-a9b0-86d6637c1da5
名前 / ファイル ライセンス アクション
S25_127.pdf S25_127.pdf (146.5 kB)
Item type 学内発行雑誌 / Departmental Bulletin Paper(1)
公開日 2016-11-18
タイトル
タイトル CpG Island Methylator Phenotype in Primary Gastric Carcinoma
言語 en
言語
言語 eng
資源タイプ
資源タイプ departmental bulletin paper
著者 TOJO, Masayuki

× TOJO, Masayuki

TOJO, Masayuki

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KONISHI, Kazuo

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KONISHI, Kazuo

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YANO, Yuichiro

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YANO, Yuichiro

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KATAGIRI, Atsushi

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KATAGIRI, Atsushi

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NOZAWA, Hisako

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NOZAWA, Hisako

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KUBOTA, Yutaro

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KUBOTA, Yutaro

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MURAMOTO, Takashi

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MURAMOTO, Takashi

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KONDA, Kenichi

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KONDA, Kenichi

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SHINMURA, Kensuke

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SHINMURA, Kensuke

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TAKIMOTO, Masafumi

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TAKIMOTO, Masafumi

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IMAWARI, Michio

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IMAWARI, Michio

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YOSHIDA, Hitoshi

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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
抄録
内容記述タイプ Abstract
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
関連タイプ isIdenticalTo
関連識別子 10.15369/sujms.25.127
出版者
出版者 Showa University Society
ISSN
収録物識別子タイプ ISSN
収録物識別子 0915-6380
出版タイプ
出版タイプ VoR
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