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

被引:25
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
相关论文
共 42 条
[1]  
Ai Xiao-Hong, 2007, Ai Zheng, V26, P357
[2]   BLEOMYCIN, VINCRISTINE, MITOMYCIN-C, AND CISPLATIN IN THE MANAGEMENT OF GYNECOLOGICAL SQUAMOUS-CELL CARCINOMAS [J].
BELINSON, JL ;
STEWART, JA ;
RICHARDS, AL ;
MCCLURE, M .
GYNECOLOGIC ONCOLOGY, 1985, 20 (03) :387-393
[3]   Immune-based mechanisms of cytotoxic chemotherapy: implications for the design of novel and rationale-based combined treatments against cancer [J].
Bracci, L. ;
Schiavoni, G. ;
Sistigu, A. ;
Belardelli, F. .
CELL DEATH AND DIFFERENTIATION, 2014, 21 (01) :15-25
[4]  
Bryniarski K, 2009, PHARMACOL REP, V61, P550, DOI 10.1016/S1734-1140(09)70098-2
[5]  
Cao Jian-Guo, 2004, World J Gastroenterol, V10, P3062
[6]  
Chen YC, 1998, J CELL PHYSIOL, V177, P324, DOI 10.1002/(SICI)1097-4652(199811)177:2<324::AID-JCP14>3.0.CO
[7]  
2-9
[8]   Treatment of metastatic cervical cancer: Future directions involving targeted agents [J].
Diaz-Padilla, Ivan ;
Monk, Bradley J. ;
Mackay, Helen J. ;
Oaknin, Ana .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2013, 85 (03) :303-314
[9]   Vitamin C promotes pluripotency of human induced pluripotent stem cells via the histone demethylase JARID1A [J].
Eid, Wassim ;
Abdel-Rehim, Wafaa .
BIOLOGICAL CHEMISTRY, 2016, 397 (11) :1205-1213
[10]   Genome-Wide Identification of CBX2 Targets: Insights in the Human Sex Development Network [J].
Eid, Wassim ;
Opitz, Lennart ;
Biason-Lauber, Anna .
MOLECULAR ENDOCRINOLOGY, 2015, 29 (02) :247-257