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  1. H-1. がん進展制御研究所
  2. h-1 10. 学術雑誌掲載論文
  3. 1. 査読済論文

Down-expression of tumor protein p53-induced nuclear protein 1 in human gastric cancer

http://hdl.handle.net/2297/11862
http://hdl.handle.net/2297/11862
8caadb45-e859-410c-a0ae-14839a0d0791
名前 / ファイル ライセンス アクション
CA-PR-MOTOO-Y-2006_691(著者最終稿).pdf CA-PR-MOTOO-Y-2006_691.pdf (820.1 kB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-05
タイトル
タイトル Down-expression of tumor protein p53-induced nuclear protein 1 in human gastric cancer
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Jiang, Pei-Hong

× Jiang, Pei-Hong

WEKO 48086

Jiang, Pei-Hong

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Motoo, Yoshiharu

× Motoo, Yoshiharu

WEKO 21362
e-Rad 80210095
研究者番号 80210095

Motoo, Yoshiharu

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Garcia, Stephane

× Garcia, Stephane

WEKO 48087

Garcia, Stephane

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Iovanna, Juan Lucio

× Iovanna, Juan Lucio

WEKO 48088

Iovanna, Juan Lucio

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Pebusque, Marie-Josephe

× Pebusque, Marie-Josephe

WEKO 48089

Pebusque, Marie-Josephe

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Sawabu, Norio

× Sawabu, Norio

WEKO 21711
e-Rad 90019969
研究者番号 90019969

Sawabu, Norio

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著者別表示 元雄, 良治

× 元雄, 良治

元雄, 良治

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澤武, 紀雄

× 澤武, 紀雄

澤武, 紀雄

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提供者所属
内容記述タイプ Other
内容記述 金沢大学がん研究所
書誌情報 World Journal of Gastroenterology

巻 12, 号 5, p. 691-696, 発行日 2006-02-07
ISSN
収録物識別子タイプ ISSN
収録物識別子 1007-9327
NCID
収録物識別子タイプ NCID
収録物識別子 AA11690631
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.3748/wjg.v12.i5.691
出版者
出版者 WJG Press
抄録
内容記述タイプ Abstract
内容記述 Aim: Overexpression of tumor protein p53-induced nuclear protein 1 (TP53INP1) induces G1 cell cycle arrest and increases p53-mediated apoptosis. To clarify the clinical importance of TP53INP1, we analyzed TP53INP1 and p53 expression in gastric cancer. Methods: TP53INP1 and p53 expression were examined using immunohistochemistry in 142 cases of gastric cancer. The apoptosis of gastric cancer cells was analyzed using the TUNEL method. The relationship between the expression of TP53INP1 and clinicopathological factors was statistically analyzed. Results: TP53INP1 was expressed in 98% (139/142 cases) of non-cancerous gastric tissues and was down-expressed in 64% (91/142 cases) of gastric cancer lesions from the same patients. TP53INP1 expression was significantly decreased (43.9%) in poorly differentiated adenocarcinoma compared with well or moderately differentiated adenocarcinoma (81.6%). Cancers invading the submucosa or deeper showed lower positively (59.1%) compared with mucosal cancers (85.2%). Decrease or loss of TP53INP1 expression was significantly correlated with lymphatic invasion (54.3% vs 82.0% without lymphatic invasion) and node-positive patients (31.3% vs 68.3% in node-negative patients). P53 was expressed in 68 (47.9%) patients of gastric cancer, whereas it was absent in normal gastric tissues. A significant association was also observed between TP53INP1 status and the level of apoptosis in tumor cells: the apoptotic index in TP53INP1-positive tissues was significantly higher than that in TP53INP1-negative portions. Finally, when survival data were analyzed, loss of TP53INP1 expression had a significant effect in predicting a poor prognosis (P=0.0006). Conclusion: TP53INP1-positive rate decreases with the progression of gastric cancer. TP53INP1 protein negativity is significantly associated with aggressive pathological phenotypes of gastric cancer. TP53INP1 is related to the apoptosis of gastric cancer cells. The decreased expression of the TP53INP1 protein may reflect the malignant grade of gastric cancer and is regarded as an adverse prognostic factor. © 2006 The WJG Press. All rights reserved.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
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