Ellagic Acid and Resveratrol Prevent the Development of Cisplatin Resistance in the Epithelial Ovarian Cancer Cell Line A2780

被引:68
|
作者
Engelke, Laura H. [1 ]
Hamacher, Alexandra [1 ]
Proksch, Peter [2 ]
Kassack, Matthias U. [1 ]
机构
[1] Univ Dusseldorf, Inst Pharmazeut & Med Chem, Univ Str 1, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Inst Pharmazeut Biol & Biotechnol, D-40225 Dusseldorf, Germany
来源
JOURNAL OF CANCER | 2016年 / 7卷 / 04期
关键词
ellagic acid; resveratrol; cisplatin; resistance development; ovarian cancer; A2780; IN-VITRO; CYCLE ARREST; APOPTOSIS; EXPRESSION; TOXICITY; GROWTH; POMEGRANATE; INHIBITION; THERAPY; AGENTS;
D O I
10.7150/jca.13754
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose. Several studies have shown that natural compounds like resveratrol or ellagic acid have anticancer and antioxidant properties and can stimulate apoptosis in many cancer cell lines. The aim of this study was to elucidate if resveratrol or ellagic acid, respectively, could improve the efficacy of cisplatin in ovarian cancer. Methods. As a cellular resistance model, the epithelial ovarian cancer cell line A2780 and its cisplatin-resistant subclone A2780CisR were used. A2780CisR was obtained by intermittent treatment of A2780 with cisplatin for 26 weekly cycles and showed a 4-6-fold increased resistance towards cisplatin compared to A2780. Results. Pretreatment with resveratrol or ellagic acid 48 h prior to treatment with cisplatin showed a moderate enhancement of cisplatin cytotoxicity in A2780CisR cells (shift factors were 1.6 for ellagic acid and 2.5 for resveratrol). However, intermittent treatment of A2780 with cisplatin for 26 weekly cycles in permanent presence of resveratrol or ellagic acid, respectively, completely prevented the development of cisplatin resistance. The generated cell lines named A2780Resv and A2780Ellag displayed functional characteristics (migration, proliferation, apoptosis, activation of ErbB3, ROS generation) similar to the parental cell line A2780. Conclusion. In conclusion, weekly intermittent treatment cycles of cisplatin-sensitive ovarian cancer cells with cisplatin retain cisplatin chemosensitivity in permanent presence of ellagic acid or resveratrol, respectively, whereas clinically relevant cisplatin chemoresistance develops in the absence of ellagic acid or resveratrol. Use of natural phenolic compounds may thus be a promising approach to prevent cisplatin resistance in ovarian cancer.
引用
收藏
页码:353 / 363
页数:11
相关论文
共 50 条
  • [21] Glycyrrhetinic Acid Inhibits Cell Growth and Induces Apoptosis in Ovarian Cancer A2780 Cells
    Haghshenas, Venus
    Fakhari, Shohreh
    Mirzaie, Sako
    Rahmani, Mohammadreza
    Farhadifar, Fariba
    Pirzadeh, Sara
    Jalili, Ali
    ADVANCED PHARMACEUTICAL BULLETIN, 2014, 4 : 437 - 441
  • [22] MiR-106a Targets Mcl-1 to Suppress Cisplatin Resistance of Ovarian Cancer A2780 Cells
    饶玉梅
    史惠蓉
    纪妹
    陈彩虹
    Current Medical Science, 2013, (04) : 567 - 572
  • [23] Extracellular Matrix Proteins Expression Profiling in Chemoresistant Variants of the A2780 Ovarian Cancer Cell Line
    Januchowski, Radoslaw
    Zawierucha, Piotr
    Rucinski, Marcin
    Nowicki, Michal
    Zabel, Maciej
    BIOMED RESEARCH INTERNATIONAL, 2014, 2014
  • [24] MiR-106a targets Mcl-1 to suppress cisplatin resistance of ovarian cancer A2780 cells
    Yu-mei Rao
    Hui-rong Shi
    Mei Ji
    Cai-hong Chen
    Journal of Huazhong University of Science and Technology [Medical Sciences], 2013, 33 : 567 - 572
  • [25] MiR-106a Targets Mcl-1 to Suppress Cisplatin Resistance of Ovarian Cancer A2780 Cells
    Rao, Yu-mei
    Shi, Hui-rong
    Ji, Mei
    Chen, Cai-hong
    JOURNAL OF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY-MEDICAL SCIENCES, 2013, 33 (04) : 567 - 572
  • [26] Liposomal cisplatin can overcome chemotherapy resistance of A2780 ovarian cancer cells by inducing the extrinsic apoptotic pathway
    Stoelting, Daniel P.
    Koch, Martin
    Wiese, Michael
    Royer, Hans-Dieter
    Bendas, Gerd
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2014, 52 (01) : 78 - 81
  • [27] Reprogramming of glutamine metabolism via glutamine synthetase silencing induces cisplatin resistance in A2780 ovarian cancer cells
    Guo, Jing
    Satoh, Kiyotoshi
    Tabata, Sho
    Mori, Masaru
    Tomita, Masaru
    Soga, Tomoyoshi
    BMC CANCER, 2021, 21 (01)
  • [28] Growth Inhibition and Apoptosis Inducing Mechanisms of Curcumin on Human Ovarian Cancer Cell Line A2780
    郑丽端
    童强松
    吴翠环
    Chinese Journal of Integrative Medicine, 2006, (02) : 126 - 131
  • [29] Reprogramming of glutamine metabolism via glutamine synthetase silencing induces cisplatin resistance in A2780 ovarian cancer cells
    Jing Guo
    Kiyotoshi Satoh
    Sho Tabata
    Masaru Mori
    Masaru Tomita
    Tomoyoshi Soga
    BMC Cancer, 21
  • [30] Growth inhibition and apoptosis inducing mechanisms of curcumin on human ovarian cancer cell line A2780
    Zheng L.-D.
    Tong Q.-S.
    Wu C.-H.
    Chinese Journal of Integrative Medicine, 2006, 12 (2) : 126 - 131