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  1. 原著論文

Purvalanol A induces apoptosis and downregulation of antiapoptotic proteins through abrogation of phosphorylation of JAK2/STAT3 and RNA polymerase II

https://repo.qst.go.jp/records/45213
https://repo.qst.go.jp/records/45213
c9449342-a4ba-46cc-99d3-7de8b9d5ee4a
Item type 学術雑誌論文 / Journal Article(1)
公開日 2008-06-24
タイトル
タイトル Purvalanol A induces apoptosis and downregulation of antiapoptotic proteins through abrogation of phosphorylation of JAK2/STAT3 and RNA polymerase II
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
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Iizuka, Daisuke

× Iizuka, Daisuke

WEKO 1011613

Iizuka, Daisuke

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Ogura, Aki

× Ogura, Aki

WEKO 1011614

Ogura, Aki

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Kuwabara, Mikinori

× Kuwabara, Mikinori

WEKO 1011615

Kuwabara, Mikinori

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Inanami, Osamu

× Inanami, Osamu

WEKO 1011616

Inanami, Osamu

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Daisuke, Iizuka

× Daisuke, Iizuka

WEKO 1011617

en Daisuke, Iizuka

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抄録
内容記述タイプ Abstract
内容記述 To clarify the mechanisms of purvalanol A in the induction of apoptosis, we investigated whether purvalanol A influenced the RNA synthesis and expression of RNA polymerase II and signal transducer and activator of transcription 3 (STAT3). When MKN45 cells were treated with 30 mumol/l purvalanol A, mitochondrial dysfunction occurred before the induction of the apoptosis and the expression of antiapoptotic proteins survivin, Bcl-XL, and Bcl-2 was reduced. The treatment with parvalanol A was also shown to reduce not only mRNA for these proteins but also global RNA synthesis. The phosphorylation of the carboxy-terminal domain of RNA polymerase II, which was involved in transcriptional regulation, was strongly inhibited by purvalanol A, followed by the partial inhibition of the expression of RNA polymerase II. Furthermore, the phosphorylation at Tyr705 of STAT3, which is known to be a phosphorylation site for Janus kinase 2 (JAK2), was completely inhibited by purvalanol A early (3 h) after drug treatment, although the phosphorylation of STAT3 at Ser727, which is a phosphorylation site for Ras/Raf/MEK and extracellular signal-regulated protein kinase 1/2, was still detectable until late (12 h) after treatment. In addition, the tyrosine phosphorylation of JAK2 was efficiently inhibited by purvalanol A. These results suggest that the inhibition of JAK2/STAT3 and RNA polymerase II is crucial in the downregulation of antiapoptotic proteins leading to the apoptotic cell death induced by parvalanol A.
書誌情報 Anti-Cancer Drugs

巻 19, 号 6, p. 565-572, 発行日 2008-06
ISSN
収録物識別子タイプ ISSN
収録物識別子 0959-4973
DOI
識別子タイプ DOI
関連識別子 10.1097/cad.0b013e3282fe330e
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