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  1. G. 附属病院
  2. g 10. 学術雑誌掲載論文
  3. 1. 査読済論文

Inhibition of epidermal growth factor-induced cell transformation and Akt activation by caffeine

http://hdl.handle.net/2297/6720
http://hdl.handle.net/2297/6720
6d5c20a2-a887-40ce-8967-431d50713c25
名前 / ファイル ライセンス アクション
PH-PR-MIYAMOTO-K-67.pdf PH-PR-MIYAMOTO-K-67.pdf (323.3 kB)
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 Inhibition of epidermal growth factor-induced cell transformation and Akt activation by caffeine
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 Nomura, Masaaki

× Nomura, Masaaki

WEKO 26700
e-Rad 20247480
研究者番号 20247480

Nomura, Masaaki

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Ichimatsu, Daisuke

× Ichimatsu, Daisuke

WEKO 44705

Ichimatsu, Daisuke

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Moritani, Shuzo

× Moritani, Shuzo

WEKO 44706

Moritani, Shuzo

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Koyama, Ichiko

× Koyama, Ichiko

WEKO 44707

Koyama, Ichiko

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Dong, Zigang

× Dong, Zigang

WEKO 44708

Dong, Zigang

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Yokogawa, Koichi

× Yokogawa, Koichi

WEKO 22233
研究者番号 50283122

Yokogawa, Koichi

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Miyamoto, Kenichi

× Miyamoto, Kenichi

WEKO 22059
研究者番号 30100514

Miyamoto, Kenichi

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提供者所属
内容記述タイプ Other
内容記述 金沢大学医学部附属病院薬剤部
書誌情報 Molecular Carcinogenesis

巻 44, 号 1, p. 67-76, 発行日 2005-09-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0899-1987
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1002/mc.20120
出版者
出版者 Wiley-Liss
抄録
内容記述タイプ Abstract
内容記述 We found that caffeine significantly inhibited epidermal growth factor (EGF)- and 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced cell transformation in the JB6 mouse epidermal cell line. The tumor promoter-induced cell transformation was also blocked by treatment with an adenosine A1 receptor antagonist, 8-phenyltheophylline (8-PTH). Caffeine slightly attenuated activation of EGF-induced activator protein 1 (AP-1) activation, which play important roles in cell transformation, but only at the highest concentration examined (1 mM). Interestingly, pretreatment with caffeine suppressed EGF-induced phosphorylation and activation of Akt and ribosomal p70 S6 protein kinase (p70 S6K), a target of Akt, without inhibiting phosphatidylinositol 3-kinase (PI3K) activation. The inhibition of Akt activation of caffeine was not a result of its adenosine receptor antagonism. Because Akt plays a key role in signal transduction pathways leading to cell proliferation and apoptosis, our results provide novel insight into possible mechanisms of the chemotherapeutic effect of caffeine. © 2005 Wiley-Liss, Inc.
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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