Synergistic Growth-Suppressive Effects of Quercetin and Cisplatin on HepG2 Human Hepatocellular Carcinoma Cells

被引:47
作者
Zhao, Ji-Ling [1 ]
Zhao, Jing [1 ]
Jiao, Hong-Jun [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 2, Dept Pharm, Zhengzhou 450052, Peoples R China
关键词
Chemotherapy; Synergism; Hepatocellular carcinoma; Quercetin; p16; CYCLE ARREST; UP-REGULATION; APOPTOSIS; INHIBITION; INDUCTION; PATHWAYS; BCL-2; P16; SENESCENCE; G(1);
D O I
10.1007/s12010-013-0561-z
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
Quercetin, a natural flavonoid, exhibits anticancer effects. The aim of this study is to determine whether the combination of quercetin with cisplatin, a conventional chemotherapeutic drug, would have synergistic suppressive effects on hepatocellular carcinoma (HCC) cells. To this end, HepG2 cells were exposed to quercetin (50 mu M) or cisplatin (10 mu M) alone or combination of both and cell proliferation and apoptosis were investigated. Our data revealed that the combination of quercetin and cisplatin was significantly (P<0.05) effective in inducing growth suppression and apoptosis in HepG2 cells, when compared with single agent treatment. Quercetin combined with cisplatin modulated the expression of numerous genes involved in cell cycle progression and apoptosis. Treatment with quercetin rather than cisplatin resulted in a marked elevation of p16 expression in HepG2 cells. Targeted reduction of p16 using RNA interference technology partially reversed quercetin-induced cell cycle G1 arrest and apoptosis in HepG2 cells. In conclusion, quercetin has suppressive activity against HCC cells through p16-mediated cell cycle arrest and apoptosis and its combination with cisplatin yielded synergistic inhibitory effects in suppressing cell growth and inducing apoptosis.
引用
收藏
页码:784 / 791
页数:8
相关论文
共 31 条
[21]   Kinetics of cisplatin binding to cellular DNA and modulations by thiol-blocking agents and thiol drugs [J].
Sadowitz, PD ;
Hubbard, BA ;
Dabrowiak, JC ;
Goodisman, J ;
Tacka, KA ;
Aktas, MK ;
Cunningham, MJ ;
Dubowy, RL ;
Souid, AK .
DRUG METABOLISM AND DISPOSITION, 2002, 30 (02) :183-190
[22]   A NEW REGULATORY MOTIF IN CELL-CYCLE CONTROL CAUSING SPECIFIC-INHIBITION OF CYCLIN-D/CDK4 [J].
SERRANO, M ;
HANNON, GJ ;
BEACH, D .
NATURE, 1993, 366 (6456) :704-707
[23]   Molecular pathways in the chemosensitization of cisplatin by quercetin in human head and neck cancer [J].
Sharma, H ;
Sen, S ;
Singh, N .
CANCER BIOLOGY & THERAPY, 2005, 4 (09) :949-955
[24]   Drug combinations with quercetin: doxorubicin plus quercetin in human breast cancer cells [J].
Staedler, Davide ;
Idrizi, Elita ;
Kenzaoui, Blanka Halamoda ;
Juillerat-Jeanneret, Lucienne .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2011, 68 (05) :1161-1172
[25]   Induction of G1/S Phase Arrest and Apoptosis by Quercetin in Human Osteosarcoma Cells [J].
Suh, Doo Kyo ;
Lee, Eul Jae ;
Kim, Hyung Chan ;
Kim, Jeong Hee .
ARCHIVES OF PHARMACAL RESEARCH, 2010, 33 (05) :781-785
[26]   Regulation of Survivin and Bcl-2 in HepG2 Cell Apoptosis Induced by Quercetin [J].
Tan, Jun ;
Wang, Bochu ;
Zhu, Liancai .
CHEMISTRY & BIODIVERSITY, 2009, 6 (07) :1101-1110
[27]   Quercetin Is Able to Demethylate the p16INK4a Gene Promoter [J].
Tan, Sainan ;
Wang, Chong ;
Lu, Cailing ;
Zhao, Baojian ;
Cui, Yi ;
Shi, Xinquan ;
Ma, Xu .
CHEMOTHERAPY, 2009, 55 (01) :6-10
[28]   Stabilization of p53 is involved in quercetin-induced cell cycle arrest and apoptosis in HepG2 cells [J].
Tanigawa, Shunsuke ;
Fujii, Makoto ;
Hou, De-Xing .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2008, 72 (03) :797-804
[29]   Comparative study of cisplatin and epirubicin in transcatheter arterial chemoembolization for hepatocellular carcinoma [J].
Yamanaka, Kenya ;
Hatano, Etsuro ;
Narita, Masato ;
Taura, Kojiro ;
Yasuchika, Kentaro ;
Nitta, Takashi ;
Arizono, Shigeki ;
Isoda, Hiroyoshi ;
Shibata, Toshiya ;
Ikai, Iwao ;
Sato, Tosiya ;
Uemoto, Shinji .
HEPATOLOGY RESEARCH, 2011, 41 (04) :303-309
[30]  
Yang JX, 2009, SAUDI MED J, V30, P35