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  1. 原著論文

Radiation engenders conversed migration and invasion in colorectal cancer cells through opposite modulation of ANXA2/ AKT /GSK3β pathway

https://repo.qst.go.jp/records/80797
https://repo.qst.go.jp/records/80797
7bdde3a9-912d-4f79-9e7c-09c422a40fed
Item type 学術雑誌論文 / Journal Article(1)
公開日 2020-05-20
タイトル
タイトル Radiation engenders conversed migration and invasion in colorectal cancer cells through opposite modulation of ANXA2/ AKT /GSK3β pathway
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 Pan, Han

× Pan, Han

WEKO 1041350

Pan, Han

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Song, Yimeng

× Song, Yimeng

WEKO 1041351

Song, Yimeng

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Zhang, Hang

× Zhang, Hang

WEKO 1041352

Zhang, Hang

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Bai, Yang

× Bai, Yang

WEKO 1041353

Bai, Yang

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Konishi, Teruaki

× Konishi, Teruaki

WEKO 1041354

Konishi, Teruaki

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Kobayashi, Alisa

× Kobayashi, Alisa

WEKO 1041355

Kobayashi, Alisa

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Shao, Chunlin

× Shao, Chunlin

WEKO 1041356

Shao, Chunlin

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Pan, Yan

× Pan, Yan

WEKO 1041357

Pan, Yan

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Teruaki, Konishi

× Teruaki, Konishi

WEKO 1041358

en Teruaki, Konishi

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Alisa, Kobayashi

× Alisa, Kobayashi

WEKO 1041359

en Alisa, Kobayashi

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抄録
内容記述タイプ Abstract
内容記述 BACKGROUND: Conventional radiation may either promote or inhibit tumor metastatic potential paradoxically, but the underlying mechanism remains vague, and the knowledge concerning the changes of metastatic potential after heavy ion radiation is still limited.
METHODSs: we detected the changes of the metastasis capacities of two colorectal cancer (CRC) cell lines after γ- or c-ion radiation, and investigated the underlying molecular mechanisms using western blot, immunoprecipitation, LC-MS/MS and siRNA transfection.
RESULTS: The change of the migration and invasion potential showed a completely reversed pattern in these two cell lines after γ-or carbon ion radiation both in vivo and vitro. Radiation induced EMT in DLD-1 cells, but MET in HCT116 cells, which was due to the opposite modulation of ANXA2/AKT/GSK3β signaling pathway in CRC cells. ANAX2 could bind directly with GSK3β and act as a negative regulator of its activation. Knocking-down ANXA2 gene not only decreased the migration in nonirradiated CRC cells, but also reversed the enhanced migration in irradiated DLD-1 cells and strengthened radiation-impaired migration in HCT116 cells.
CONCLUSION: The change of cellular motility after radiation is independent of radiation type, but is correlated with the inherent of cells, and ANXA2 is applicable to be a potential target for radiotherapy.
書誌情報 American Journal of Cancer Research

巻 11, 号 1, p. 61-78, 発行日 2020-10
出版者
出版者 e-Century Publishing Corporation
ISSN
収録物識別子タイプ ISSN
収録物識別子 2156-6976
関連サイト
識別子タイプ URI
関連識別子 https://e-century.us/files/ajcr/11/1/ajcr0121599.pdf
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