Livistona chinensis seed suppresses hepatocellular carcinoma growth through promotion of mitochondrial-dependent apoptosis

被引:13
作者
Lin, Wei [1 ,2 ]
Zhao, Jinyan [1 ,2 ]
Cao, Zhiyun [1 ]
Zhuang, Qunchuan [1 ,2 ]
Zheng, Liangpu [1 ,2 ]
Cai, Qiaoyan [1 ,2 ]
Chen, Daxin [1 ,2 ]
Wang, Lili [1 ,2 ]
Hong, Zhenfeng [1 ]
Peng, Jun [1 ,2 ]
机构
[1] Fujian Univ Tradit Chinese Med, Acad Integrat Med, Fuzhou 350122, Fujian, Peoples R China
[2] Fujian Univ Tradit Chinese Med, Fujian Key Lab Integrat Med Geriatr, Fuzhou 350122, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; apoptosis; herbal medicine; mitochondrion; Livistona chinensis seed; BCL-2; FAMILY-MEMBERS; CYTOCHROME-C; RISK-FACTORS; NATURAL-PRODUCTS; BAX; RELEASE; EPIDEMIOLOGY; ANGIOGENESIS; CYTOSOL; DEATH;
D O I
10.3892/or.2013.2319
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Livistona chinensis seed has been used for centuries to clinically treat various types of cancer. However, the precise mechanism of its anticancer activity remains to be elucidated. In the present study, we evaluated the efficacy of the ethanol extract of Livistona chinensis seed (EELC) against tumor growth using a hepatocellular carcinoma (HCC) mouse xenograft model and an HCC cell line, HepG2, and investigated the molecular mechanisms mediating its biological activities. We found that EELC inhibited HCC growth both in vivo and in vitro, without apparent signs of toxicity. In addition, EELC treatment resulted in the induction of HCC cell apoptosis. Moreover, EELC-induced apoptosis was accompanied by the loss of mitochondrial membrane potential, activation of caspase-9 and caspase-3, and increase in the proapoptotic Bax/Bcl-2 ratio. Our findings suggest that promotion of mitochondrial-dependent apoptosis in cancer cells may be one of the mechanisms by which the Livistona chinensis seed is effective in cancer treatment.
引用
收藏
页码:1859 / 1866
页数:8
相关论文
共 36 条
  • [1] Abou-Alfa Ghassan K, 2008, Gastrointest Cancer Res, V2, P64
  • [2] The Bcl-2 apoptotic switch in cancer development and therapy
    Adams, J. M.
    Cory, S.
    [J]. ONCOGENE, 2007, 26 (09) : 1324 - 1337
  • [3] Bax oligomerization is required for channel-forming activity in liposomes and to trigger cytochrome c release from mitochondria
    Antonsson, B
    Montessuit, S
    Lauper, S
    Eskes, R
    Martinou, JC
    [J]. BIOCHEMICAL JOURNAL, 2000, 345 : 271 - 278
  • [4] Genotoxicity of several clinically used topoisomerase II inhibitors
    Boos, G
    Stopper, H
    [J]. TOXICOLOGY LETTERS, 2000, 116 (1-2) : 7 - 16
  • [5] Preface - Bcl-2 family members: integrators of survival and death
    Borner, C
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1644 (2-3): : 71 - 72
  • [6] Hedyotis diffusa Willd Inhibits Colorectal Cancer Growth in Vivo via Inhibition of STAT3 Signaling Pathway
    Cai, Qiaoyan
    Lin, Jiumao
    Wei, Lihui
    Zhang, Ling
    Wang, Lili
    Zhan, Youzhi
    Zeng, Jianwei
    Xu, Wei
    Shen, Aling
    Hong, Zhenfeng
    Peng, Jun
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2012, 13 (05) : 6117 - 6128
  • [7] Cheung S, 2005, ONCOL REP, V14, P1331
  • [8] The BCL2 family: Regulators of the cellular life-or-death switch
    Cory, S
    Adams, JM
    [J]. NATURE REVIEWS CANCER, 2002, 2 (09) : 647 - 656
  • [9] Hepatocellular carcinoma: Epidemiology, risk factors and pathogenesis
    Gomaa, Asmaa Ibrahim
    Khan, Shahid A.
    Toledano, Mireille B.
    Waked, Imam
    Taylor-Robinson, Simon D.
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (27) : 4300 - 4308
  • [10] Natural products as leads to anticancer drugs
    Gordaliza, M.
    [J]. CLINICAL & TRANSLATIONAL ONCOLOGY, 2007, 9 (12) : 767 - 776