Neferine Enhances the Antitumor Effect of Mitomycin-C in Hela Cells Through the Activation of p38-MAPK Pathway

被引:24
|
作者
Eid, Wassim [1 ,2 ]
Abdel-Rehim, Wafaa [2 ]
机构
[1] Univ Fribourg, Dept Med, Div Endocrinol, Chemin Musee 5, CH-1700 Fribourg, Switzerland
[2] Univ Alexandria, Med Res Inst, Dept Biochem, Alexandria, Egypt
关键词
NEFERINE; MITOMYCIN C; CERVICAL CANCER; p38; MAPK; ROS; LOTUS SEED EMBRYO; OXIDATIVE STRESS; CERVICAL-CANCER; CONCURRENT RADIATION; APOPTOSIS; CYCLOPHOSPHAMIDE; PROLIFERATION; CHEMOTHERAPY; GLUTATHIONE; BLEOMYCIN;
D O I
10.1002/jcb.26006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current treatment options for patients with cervical cancer are far from desirable, with cervical cancer remaining to be one of the leading causes of cancer-related deaths; this highlights the need to formulate strategies that enhance the efficacy of available therapies. Mitomycin C (MMC) possesses antitumor effect in different cancers. However, the efficacy of MMC depends on other drugs in the combinational therapy and is often hampered by side-effects. Neferine, a natural alkaloid, exhibits antitumor effects in various cancers. In this study, we questioned the antitumor efficacy of a combinational treatment of neferine and MMC in cervical cancer cells. We found that neferine prominently enhanced the antitumor effects of MMC; this effect was dependent on the induction of apoptosis. Furthermore, we also provide a mechanistic insight and show that the enhanced apoptosis was a result of at least in part, a sustained activation of the p38 MAPK pathway in a ROS-dependent mechanism. Our results therefore demonstrate the potentiated antitumor effect of neferine and MMC on cervical cancer cells and may offer a potential treatment strategy for patients with cervical cancer. (C) 2017 Wiley Periodicals, Inc.
引用
收藏
页码:3472 / 3479
页数:8
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