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  1. 原著論文

Basic study on SH2 domain of Grb2 as a molecular probe for detection of RTK activation

https://repo.qst.go.jp/records/45996
https://repo.qst.go.jp/records/45996
e058a924-4ef5-4742-92b2-b9aec5d04788
Item type 学術雑誌論文 / Journal Article(1)
公開日 2011-02-07
タイトル
タイトル Basic study on SH2 domain of Grb2 as a molecular probe for detection of RTK activation
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 Saito, Yuriko

× Saito, Yuriko

WEKO 457751

Saito, Yuriko

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Furukawa, Takako

× Furukawa, Takako

WEKO 457752

Furukawa, Takako

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Arano, Yasushi

× Arano, Yasushi

WEKO 457753

Arano, Yasushi

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Fujibayashi, Yasuhisa

× Fujibayashi, Yasuhisa

WEKO 457754

Fujibayashi, Yasuhisa

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 457755

Saga, Tsuneo

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齋藤 有里子

× 齋藤 有里子

WEKO 457756

en 齋藤 有里子

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古川 高子

× 古川 高子

WEKO 457757

en 古川 高子

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荒野 泰

× 荒野 泰

WEKO 457758

en 荒野 泰

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藤林 康久

× 藤林 康久

WEKO 457759

en 藤林 康久

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佐賀 恒夫

× 佐賀 恒夫

WEKO 457760

en 佐賀 恒夫

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抄録
内容記述タイプ Abstract
内容記述 Epidermal growth factor receptor (EGFR) and other receptor tyrosine kinases (RTKs) are overexpressed and/or mutated in various cancers and their abnormal activation
is implicated in carcinogenesis. We explored the possibility of generating an imaging probe for RTK activation using the SH2 domain of Grb2 for cancer characterization. For cell penetration, molecular analysis and radiolabeling, the SH2 domain was fused with TAT, flag and tyrosine residue, respectively (termed TSF). We analyzed TSF characteristics in cells such as cellular uptake, stability and localization.
After uptake into EGFR-expressing cells, TSF was found to be binding to phosphorylated-EGFR, which increased by stimulation with EGF. TSF was co-localized with EGFR in EGFR-activated cells, while it was localized as dots in cytosol in EGFR-non-activated cells. Cellular retention time of TSF was significantly extended under EGFR activation with EGF stimuli and reduced under the treatment with a tyrosine kinase inhibitor, Tyrphostin AG1478. In conclusion, the SH2 domain of Grb2 has the potential to be used as a binding component of a probe to detect activated-RTK and to evaluate the effect of kinase inhibitors on RTK activation.
書誌情報 International Journal of Oncology

巻 37, 号 2, p. 281-287, 発行日 2010-06
ISSN
収録物識別子タイプ ISSN
収録物識別子 1019-6439
DOI
識別子タイプ DOI
関連識別子 10.3892/ijo_00000676
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