中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Morphine inhibits doxorubicin-induced reactive oxygen species generation and nuclear factor kappa B transcriptional activation in neuroblastoma SH-SY5Y cells

文献类型:期刊论文

作者Lin, Xin; Li, Qing; Wang, Yu-Jun; Ju, Ya-Wen; Chi, Zhi-Qiang; Wang, Min-Wei; Liu, Jing-Gen
刊名BIOCHEMICAL JOURNAL
出版日期2007-09-01
卷号406页码:215-221
关键词apoptosis doxorubicin (DOX) morphine nuclear factor kappa B reactive oxygen species SH-SY5Y cell
ISSN号0264-6021
DOI10.1042/BJ20070186
文献子类Article
英文摘要Morphine is recommended as a first-line opioid analgesic in the pain management of cancer patients. Accumulating evidence shows that morphine has anti-apoptotic activity, but its impact on the therapeutic applications of antineoplastic drugs is not well known. The present study was undertaken to test the hypothesis that morphine might antagonize the pro-apoptotic activity of DOX (doxorubicin), a commonly used antitumour drug for the treatment of neuroblastoma, in cultured SH-SY5Y cells. In the present study we demonstrated that morphine suppressed DOX-induced inhibition of cell proliferation and programmed cell death in a concentration-dependent, and naloxone as well as pertussis toxin-irreversible, manner. Further studies showed that morphine inhibited ROS (reactive oxygen species) generation, and prevented DOX-mediated caspase-3 activation, cytochrome c release and changes of Bax and Bc1-2 protein expression. The antioxidant NAC (N-acetylcysteine) also showed the same effects as morphine on DOX-induced ROS generation, caspase-3 activation and cytochrome c release and changes in Bax (Bc1-2-associated X protein) and Bc1-2 protein expression. Additionally, morphine was found to suppress DOX-induced NF-kappa B (nuclear factor kappa B) transcriptional activation via a reduction Of I kappa B alpha (inhibitor of nuclear factor kappa B) degradation. These present findings support the hypothesis that morphine can inhibit DOX-induced neuroblastoma cell apoptosis by the inhibition of ROS generation and mitochondrial cytochrome c release, as well as by blockade of NF-kappa B transcriptional activation, and suggests that morphine might have an impact on the antitumour efficiency of DOX.
WOS关键词CYTOCHROME-C RELEASE ; INDUCED APOPTOSIS ; HYDROGEN-PEROXIDE ; TUMOR-GROWTH ; CASPASE-3 ACTIVATION ; OXIDATIVE STRESS ; IN-VITRO ; MECHANISM ; DEATH ; ALPHA
WOS研究方向Biochemistry & Molecular Biology
语种英语
WOS记录号WOS:000249181200004
出版者PORTLAND PRESS LTD
源URL[http://119.78.100.183/handle/2S10ELR8/273152]  
专题药理学第二研究室
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Liu, Jing-Gen
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
2.Sheyang Pharmaceut Univ, Dept Pharmacol, New Delhi 110016, India
推荐引用方式
GB/T 7714
Lin, Xin,Li, Qing,Wang, Yu-Jun,et al. Morphine inhibits doxorubicin-induced reactive oxygen species generation and nuclear factor kappa B transcriptional activation in neuroblastoma SH-SY5Y cells[J]. BIOCHEMICAL JOURNAL,2007,406:215-221.
APA Lin, Xin.,Li, Qing.,Wang, Yu-Jun.,Ju, Ya-Wen.,Chi, Zhi-Qiang.,...&Liu, Jing-Gen.(2007).Morphine inhibits doxorubicin-induced reactive oxygen species generation and nuclear factor kappa B transcriptional activation in neuroblastoma SH-SY5Y cells.BIOCHEMICAL JOURNAL,406,215-221.
MLA Lin, Xin,et al."Morphine inhibits doxorubicin-induced reactive oxygen species generation and nuclear factor kappa B transcriptional activation in neuroblastoma SH-SY5Y cells".BIOCHEMICAL JOURNAL 406(2007):215-221.

入库方式: OAI收割

来源:上海药物研究所

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