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  1. 原著論文

Quantitative proteomic analysis for radiation-induced cell cycle suspension in 92-1 melanoma cell line

https://repo.qst.go.jp/records/46751
https://repo.qst.go.jp/records/46751
ce3dade9-aa01-4357-8bba-f9ed059c60ef
Item type 学術雑誌論文 / Journal Article(1)
公開日 2014-05-12
タイトル
タイトル Quantitative proteomic analysis for radiation-induced cell cycle suspension in 92-1 melanoma cell line
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 WANG, Fengling

× WANG, Fengling

WEKO 466227

WANG, Fengling

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BING, Zhitong

× BING, Zhitong

WEKO 466228

BING, Zhitong

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ZHANG, Yanan

× ZHANG, Yanan

WEKO 466229

ZHANG, Yanan

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AO, Bin

× AO, Bin

WEKO 466230

AO, Bin

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ZHANG, Sheng

× ZHANG, Sheng

WEKO 466231

ZHANG, Sheng

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YE, Caiyong

× YE, Caiyong

WEKO 466232

YE, Caiyong

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HE, Jinpeng

× HE, Jinpeng

WEKO 466233

HE, Jinpeng

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DING, Nan

× DING, Nan

WEKO 466234

DING, Nan

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YE, Wenling

× YE, Wenling

WEKO 466235

YE, Wenling

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XIONG, Jie

× XIONG, Jie

WEKO 466236

XIONG, Jie

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SUN, Jintu

× SUN, Jintu

WEKO 466237

SUN, Jintu

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Furusawa, Yoshiya

× Furusawa, Yoshiya

WEKO 466238

Furusawa, Yoshiya

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Zhou, Guangming

× Zhou, Guangming

WEKO 466239

Zhou, Guangming

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YANG, Lei

× YANG, Lei

WEKO 466240

YANG, Lei

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古澤 佳也

× 古澤 佳也

WEKO 466241

en 古澤 佳也

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Zhou Guangming

× Zhou Guangming

WEKO 466242

en Zhou Guangming

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抄録
内容記述タイプ Abstract
内容記述 Melanoma is a malignant tumor with high invasive and metastatic properties. Though radiation is the major therapy for melanoma, its radio-resistance has been shown to severely influence the clinical outcome. So it is imperative to enhance the sensitivity of uveal melanoma cells to radiotherapy. Previously, we found that the cell cycle of 92-1 uveal melanoma cells was suspended and remained unchanged for up to 5 days after exposure to 10 Gy of X-rays, which might be relevant to the high radio-sensitivity of 92-1 cells. To further investigate the cell cycle suspension-associated proteins, we employed two analyses with stable isotope labeling with amino acids in cell culture technology and two-dimensional liquid chromatography tandem mass spectrometry. Cells were incubated for 15 h or 48 h after irradiation with 10 Gy of X-rays. We identified a total of 737 proteins at 15 h (Group A) and 530 proteins at 48 h post-irradiation (Group B). The gene ontology biological pathway was used to obtain a systems level view of proteome changes in 92-1cells under cell cycle suspension. We further selected the significantly changed proteins for investigation of their potential contribution to cell cycle suspension, growth arrest and cell senescence. These proteins are involved in the cell cycle, stress response, glycolysis and the tricarboxylic acid cycle, etc. Our study expected to reveal potential marker proteins associated with cell suspension induced by irradiation, which might contribute to understanding the mechanism beyond the cell cycle suspension.
書誌情報 Journal of Radiation Research

巻 54, p. 649-662, 発行日 2013-02
ISSN
収録物識別子タイプ ISSN
収録物識別子 0449-3060
DOI
識別子タイプ DOI
関連識別子 10.1093/jrr/rrt010
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