中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Downregulation of Nrf2 promotes radiation-induced apoptosis through Nrf2 mediated Notch signaling in non-small cell lung cancer cells

文献类型:期刊论文

作者Zhao, Qiuyue1,2,3,4; Mao, Aihong1,2,3,4; Yan, Jiawei1,2,3,4; Sun, Chao1,2,3; Di, Cuixia1,2,3; Zhou, Xin1,2,3; Li, Hongyan1,2,3; Guo, Ruoshui5; Zhang, Hong1,2,3
刊名INTERNATIONAL JOURNAL OF ONCOLOGY
出版日期2016-02-01
卷号48页码:765-773
关键词nuclear factor erythroid-2-related factor 2 ionizing radiation ROS Notch1 lung cancer
ISSN号1019-6439
DOI10.3892/ijo.2015.3301
英文摘要The nuclear factor erythroid-2-related factor 2 (Nrf2) is a crucial regulator of the cellular antioxidant system. Nrf2 is often constitutively activated in non-small cell lung cancer (NSCLC) cell lines, which promotes cytoprotection against oxidative stress and xenobiotics. Notch1 signaling is critically implicated in cell fate determination. It has been reported that Nf2 strongly regulates Notch1 activity. However, the role of Nrf2 mediated Notch1 signaling in response to ionizing radiation (IR) remains elusive. We report that knockdown of Nrf2 promotes radiation-induced apoptosis through Nrf2 mediated Notch1 signaling in NSCLC cells. IR activated Nrf2 in a dose-dependent manner and the expression of Nrf2 was significantly elevated at 4 h after exposure. RNAi-mediated reduction of Nrf2 significantly increased endogenous ROS levels, and decreased the expression of glutamate cysteine ligase catalytic subunit (GCLC), heme oxygenase-1 (HO-1) and NAD (P) H quinine oxidoreductase-1 (NQO1) in irradiated cells. Furthermore, decrease in Nrf2 expression significantly dampened Notch1 expression following ionizing radiation exposure, and potentiated IR-induced cellular apoptosis. These results demonstrated that Nrf2 could be activated by ionizing radiation, knockdown of Nrf2 could promote radiation induced apoptosis and Nrf2-mediated Notch signaling is an important determinant in radioresistance of lung cancer cells.
WOS关键词GENE-EXPRESSION ; HEPATOCELLULAR-CARCINOMA ; NRF2/KEAP1 PATHWAY ; SYSTEMIC-SCLEROSIS ; STEM-CELLS ; IN-VIVO ; ACTIVATION ; SURVIVAL ; RADIORESISTANCE ; GROWTH
资助项目Key Program of National Natural Science Foundation of China[U1432248] ; National Natural Science Foundation of China[11105203] ; National Natural Science Foundation of China[11305224]
WOS研究方向Oncology
语种英语
WOS记录号WOS:000366897500033
出版者SPANDIDOS PUBL LTD
资助机构Key Program of National Natural Science Foundation of China ; National Natural Science Foundation of China
源URL[http://119.78.100.186/handle/113462/41274]  
专题中国科学院近代物理研究所
通讯作者Zhang, Hong
作者单位1.Chinese Acad Sci, Inst Modern Phys, Lanzhou 730000, Gansu, Peoples R China
2.Chinese Acad Sci, Key Lab Heavy Ion Radiat Med, Lanzhou 730000, Gansu, Peoples R China
3.Key Lab Heavy Ion Radiat Med Gansu Prov, Lanzhou 730000, Gansu, Peoples R China
4.Univ Chinese Acad Sci, Beijing 100039, Peoples R China
5.South China Agr Univ, Guangzhou 510642, Guangdong, Peoples R China
推荐引用方式
GB/T 7714
Zhao, Qiuyue,Mao, Aihong,Yan, Jiawei,et al. Downregulation of Nrf2 promotes radiation-induced apoptosis through Nrf2 mediated Notch signaling in non-small cell lung cancer cells[J]. INTERNATIONAL JOURNAL OF ONCOLOGY,2016,48:765-773.
APA Zhao, Qiuyue.,Mao, Aihong.,Yan, Jiawei.,Sun, Chao.,Di, Cuixia.,...&Zhang, Hong.(2016).Downregulation of Nrf2 promotes radiation-induced apoptosis through Nrf2 mediated Notch signaling in non-small cell lung cancer cells.INTERNATIONAL JOURNAL OF ONCOLOGY,48,765-773.
MLA Zhao, Qiuyue,et al."Downregulation of Nrf2 promotes radiation-induced apoptosis through Nrf2 mediated Notch signaling in non-small cell lung cancer cells".INTERNATIONAL JOURNAL OF ONCOLOGY 48(2016):765-773.

入库方式: OAI收割

来源:近代物理研究所

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