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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Activation of ERK/IER3/PP2A-B56γ-positive feedback loop in lung adenocarcinoma by allelic deletion of B56γ gene

http://hdl.handle.net/2297/45517
http://hdl.handle.net/2297/45517
62c30af4-ef8a-446f-96d9-1049d9ce9961
名前 / ファイル ライセンス アクション
ME-PR-KAWAHARA-E-2635.pdf ME-PR-KAWAHARA-E-2635.pdf (577.8 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Activation of ERK/IER3/PP2A-B56γ-positive feedback loop in lung adenocarcinoma by allelic deletion of B56γ gene
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 Ito, Tomoko

× Ito, Tomoko

WEKO 24678

Ito, Tomoko

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Ozaki, Satoru

× Ozaki, Satoru

WEKO 24679
金沢大学研究者情報 40401921
研究者番号 40401921

Ozaki, Satoru

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Chanasong, Rachanee

× Chanasong, Rachanee

WEKO 24680

Chanasong, Rachanee

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Mizutani, Yuki

× Mizutani, Yuki

WEKO 24681

Mizutani, Yuki

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Oyama, Takeru

× Oyama, Takeru

WEKO 406
金沢大学研究者情報 00515314
研究者番号 00515314

Oyama, Takeru

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Sakurai, Hiroshi

× Sakurai, Hiroshi

WEKO 15643
e-Rad 00225848
金沢大学研究者情報 00225848
研究者番号 00225848

Sakurai, Hiroshi

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Matsumoto, Isao

× Matsumoto, Isao

WEKO 292
e-Rad 80361989
金沢大学研究者情報 80361989
研究者番号 80361989

Matsumoto, Isao

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Takemura, Hirofumi

× Takemura, Hirofumi

WEKO 218
e-Rad 20242521
金沢大学研究者情報 20242521
研究者番号 20242521

Takemura, Hirofumi

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Kawahara, Ei

× Kawahara, Ei

WEKO 661
e-Rad 90161348
研究者番号 90161348

Kawahara, Ei

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書誌情報 Oncology Reports

巻 35, 号 5, p. 2635-2642, 発行日 2016-03-30
ISSN
収録物識別子タイプ ISSN
収録物識別子 1021-335X
NCID
収録物識別子タイプ NCID
収録物識別子 AA11016405
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.3892/or.2016.4677
出版者
出版者 Spandidos Publications
抄録
内容記述タイプ Abstract
内容記述 In order to investigate the involvement of the IER3/ PP2A-B56γ/ERK-positive feedback loop, which leads to sustained phosphorylation/activation of ERK in carcinogenesis, we immunohistochemically examined the expression of IER3 and phosphorylated ERK in lung tumor tissues. IER3 was overexpressed in all cases of adenocarcinomas examined, but was not overexpressed in squamous cell carcinomas. Phosphorylated ERK (pERK) was also overexpressed in almost all adenocarcinomas. EGFR and RAS, whose gene product is located upstream of ERK, were sequenced. Activating mutation of EGFR, which is a possible cause of overexpression of IER3 and pERK, was found only in 5 adenocarcinomas (42%). No mutation of RAS was found. We further examined the sequences of all exons of B56γ gene (PPP2R5C) and IER3, but no mutation was found. Using a single nucleotide insertion in intron 1 of PPP2R5C, which was found in the process of sequencing, allelic deletion of PPP2R5C was examined. Eight cases were informative (67%), and the deletion was found in 4 of them (50%). Three cases having deletion of PPP2R5C did not have EGFR mutation. Finally, PPP2R5C deletion or EGFR mutation that could be responsible for IER3/pERK overexpression was found in at least 8 cases (67% or more). This is the first report of a high incidence of deletion of PPP2R5C in human carcinomas.
内容記述
内容記述タイプ Other
内容記述 Embargo Period 12 months
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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