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Upregulation of HOXA10 in gastric cancer with the intestinal mucin phenotype: reduction during tumor progression and favorable prognosis

https://hiroshima.repo.nii.ac.jp/records/2006561
https://hiroshima.repo.nii.ac.jp/records/2006561
428bf98b-7303-4928-8c16-f35cf68d79a7
名前 / ファイル ライセンス アクション
Carcinogenesis_33_1081.pdf Carcinogenesis_33_1081.pdf (439.2 KB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Upregulation of HOXA10 in gastric cancer with the intestinal mucin phenotype: reduction during tumor progression and favorable prognosis
言語 en
作成者 Sentani, Kazuhiro

× Sentani, Kazuhiro

en Sentani, Kazuhiro

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Oue, Naohide

× Oue, Naohide

en Oue, Naohide

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Naito, Yutaka

× Naito, Yutaka

en Naito, Yutaka

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Sakamoto, Naoya

× Sakamoto, Naoya

en Sakamoto, Naoya

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Anami, Katsuhiro

× Anami, Katsuhiro

en Anami, Katsuhiro

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Oo, Htoo Zarni

× Oo, Htoo Zarni

en Oo, Htoo Zarni

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Uraoka, Naohiro

× Uraoka, Naohiro

en Uraoka, Naohiro

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Aoyagi, Kazuhiko

× Aoyagi, Kazuhiko

en Aoyagi, Kazuhiko

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Sasaki, Hiroki

× Sasaki, Hiroki

en Sasaki, Hiroki

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Yasui, Wataru

× Yasui, Wataru

en Yasui, Wataru

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 (c) The Author 2012. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com
主題
主題Scheme NDC
主題 490
内容記述
内容記述 Gastric cancer (GC) is one of the most common malignancies worldwide. Better knowledge of the changes in gene expression that occur during gastric carcinogenesis may lead to improvements in diagnosis, treatment and prevention. In this study, we screened for genes upregulated in GC by comparing gene expression profiles from microarray and serial analysis of gene expression and identified the HOXA10 gene. The aim of the present study was to investigate the significance of HOXA10 in GC. Immunohistochemical analysis demonstrated that 221 (30%) of 749 GC cases were positive for HOXA10, whereas HOXA10 was scarcely expressed in non-neoplastic gastric mucosa except in the case of intestinal metaplasia. Next, we analyzed the relationship between HOXA10 expression and clinicopathological characteristics. HOXA10 expression showed a significant inverse correlation with the depth of invasion and was observed more frequently in the differentiated type of GC than in the undifferentiated type of GC. HOXA10 expression was associated with GC with the intestinal mucin phenotype and correlated with CDX2 expression. Furthermore, the prognosis of patients with positive HOXA10 expression was significantly better than in the negative expression cases. 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyl tetrazolium bromide and wound healing assay revealed that knockdown of HOXA10 in GC cells by short interfering RNA transfection significantly increased viability and motility relative to the negative control, indicating that HOXA10 expression inhibits cell growth and motility. These results suggest that expression of HOXA10 may be a key regulator for GC with the intestinal mucin phenotype.
言語 en
出版者
出版者 Oxford University Press
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
出版タイプ
出版タイプ AO
出版タイプResource http://purl.org/coar/version/c_b1a7d7d4d402bcce
関連情報
識別子タイプ DOI
関連識別子 10.1093/carcin/bgs121
関連情報
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1093/carcin/bgs121
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0143-3334
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA12072343
開始ページ
開始ページ 1081
書誌情報 Carcinogenesis
Carcinogenesis

巻 33, 号 5, p. 1081-1088, 発行日 2012
旧ID 34787
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