Berberine induces apoptosis via the mitochondrial pathway in liver cancer cells

被引:87
作者
Yip, Novia K. Y. [1 ]
Ho, W. S. [1 ]
机构
[1] Chinese Univ Hong Kong, Sch Life Sci, Shatin, Hong Kong, Peoples R China
关键词
berberine; apoptosis; Huh7; anti-proliferative; caspase cascade; TRANSCRIPTION; PROTEINS; BINDING; BCL-2;
D O I
10.3892/or.2013.2543
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Current chemotherapeutic strategies for liver cancer have limitations. Thus, the demand for complementary medicine is warranted. We evaluated the antitumor potential of berberine, a naturally bioactive phytochemical from Coptis chinensis Franch against Huh7 cancer cells and WRL68 liver cells. The antitumor activity of berberine was evaluated by flow cytometry. The caspase-dependent pathway was assessed using western blot analysis. Results showed that berberine induced the apoptosis of liver cancer cells through procaspase-9, and its effector caspases, procaspase-3 and procaspase-7. Flow cytometry revealed that berberine caused cell cycle arrest at the M/G1 phase. The results of reverse transcription-polymerase chain reaction showed that berberine increased the expression of Bax, which resulted in the activation of the caspase cascade. The present findings demonstrated that berberine induces the apoptosis of Huh7 cells via the mitochondrial pathway.
引用
收藏
页码:1107 / 1112
页数:6
相关论文
共 17 条
[1]
A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[2]
Role of poly(ADP-ribose) polymerase (PARP) cleavage in apoptosis - Caspase 3-resistant PARP mutant increases rates of apoptosis in transfected cells [J].
Boulares, AH ;
Yakovlev, AG ;
Ivanova, V ;
Stoica, BA ;
Wang, GP ;
Iyer, S ;
Smulson, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) :22932-22940
[3]
Cancer Prevention after Cancer: Changing the Paradigm-a Report from the American Society of Preventive Oncology [J].
Campo, Rebecca A. ;
Rowland, Julia H. ;
Irwin, Melinda L. ;
Nathan, Paul C. ;
Gritz, Ellen R. ;
Kinney, Anita Y. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2011, 20 (10) :2317-2324
[4]
Mammalian caspases: Structure, activation, substrates, and functions during apoptosis [J].
Earnshaw, WC ;
Martins, LM ;
Kaufmann, SH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :383-424
[5]
Epidemiology of hepatocellular carcinoma in USA [J].
El-Serag, Hashem B. .
HEPATOLOGY RESEARCH, 2007, 37 :S88-S94
[6]
Targeting apoptosis pathways in cancer therapy [J].
Ghobrial, IM ;
Witzig, TE ;
Adjei, AA .
CA-A CANCER JOURNAL FOR CLINICIANS, 2005, 55 (03) :178-194
[7]
harakiri, a novel regulator of cell death, encodes a protein that activates apoptosis and interacts selectively with survival-promoting proteins Bcl-2 and Bcl-X-L [J].
Inohara, N ;
Ding, LY ;
Chen, S ;
Nunez, G .
EMBO JOURNAL, 1997, 16 (07) :1686-1694
[8]
AKT/PKB phosphorylation of p21Cip/WAF1 enhances protein stability of p21Cip/WAF1 and promotes cell survival [J].
Li, Y ;
Dowbenko, D ;
Lasky, LA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) :11352-11361
[9]
CELL-CYCLE INHIBITION BY INDEPENDENT CDK AND PCNA BINDING DOMAINS IN P21(CIP1) [J].
LUO, Y ;
HURWITZ, J ;
MASSAGUE, J .
NATURE, 1995, 375 (6527) :159-161
[10]
Berberine inhibits cyclin D1 expression via suppressed binding of AP-1 transcription factors to CCND1 AP-1 motif [J].
Luo, Ye ;
Hao, Yu ;
Shi, Tai-ping ;
Deng, Wei-wei ;
Li, Na .
ACTA PHARMACOLOGICA SINICA, 2008, 29 (05) :628-633