JR6, a new compound isolated from Justicia procumbens, induces apoptosis in human bladder cancer EJ cells through caspase-dependent pathway

被引:32
作者
He, Xiao-Li [1 ,2 ]
Zhang, Peng [3 ]
Dong, Xian-Zhe [3 ]
Yang, Mei-Hua [1 ,2 ]
Chen, Shi-Lin [1 ,2 ]
Bi, Ming-Gang [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Med Plant Dev, Res Ctr Pharmacol & Toxicol, Beijing 100193, Peoples R China
[2] Peking Union Med Coll, Beijing 100193, Peoples R China
[3] Harbin Univ Commerce, Life Sci & Environm Sci Res Ctr, Inst Mat Med, Postdoctoral Res Stn, Harbin 150076, Peoples R China
基金
中国国家自然科学基金;
关键词
JR6; Caspase; Apoptosis; Mitochondria; Reactive oxygen species; Bladder cancer; FREE-RADICALS; NITRIC-OXIDE; IN-VIVO; MITOCHONDRIA; SENESCENCE; GENERATION; LIGNANS; DEATH; P53;
D O I
10.1016/j.jep.2012.09.010
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Numerous efforts have been conducted in searching for effective agents against cancer, in particular from herbal medicines. Justicia procumbens is a traditional herbal remedy which was produced in the south-western and southern provinces of China and Taiwan province used to treat fever, pain, and cancer. Here, we identified a new compound 6'-hydroxy justicidin A (JR6) from Justicia procumbens, which showed obvious anti-cancer effects. Materials and methods: The cytotoxicity activity was assayed using MIT and SRB. Intracellular ROS visualization and quantification were acquired by using a laser scanning confocal microscopy. Apoptosis was measured using a propidium iodide (PI) apoptosis detection kit by flow cytometry. Activation of caspases (caspase-3, caspase-8, and caspase-9) was evaluated respectively using GloMax luminescence detector and Caspase-Glo 3,8,9 assay kits. Loss of mitochondrial membrane potential was observed by microscopy using JC-1 dye. Quantitative real-time PCR analysis was employed to detect the expression of protein associated with cell death. Results: JR6 remarkably inhibited growth in human bladder cancer EJ cells by decreasing cell proliferation, reduced the SOD activity, increased the content of reactive oxygen species (ROS), and induced apoptosis. Activation of caspase-8, caspase-9, and the subsequent activation of caspase-3 indicated that JR6 may be inducing intrinsic and extrinsic apoptosis pathways. Caspase-3, caspase-8, and caspase-9 inhibition rendered this extract ineffective, thus JR6-induced apoptosis is caspase-dependent. JR6 also disrupted the mitochondrial membrane potential (Delta psi m) and unregulated the Bax and p53 expressions in EJ cells. Conclusion: These observations suggest that JR6 induce apoptosis through caspase-dependent pathway in human bladder cancer EJ cells, emphasizing the importance of this traditional medicine and thus presents a potential novel alternative to bladder cancer therapy. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:284 / 292
页数:9
相关论文
共 31 条
[1]  
AHLERING TE, 1987, CANCER RES, V47, P6660
[2]  
Azad MB, 2009, ANTIOXID REDOX SIGN, V11, P777, DOI 10.1089/ARS.2008.2270
[3]  
Bechtel W, 2009, ANTICANCER RES, V29, P4559
[4]  
Cadenas Enrique, 2004, Molecular Aspects of Medicine, V25, P17, DOI 10.1016/j.mam.2004.02.005
[5]   Mitochondrial factors with dual roles in death and survival [J].
Cheng, W. -C ;
Berman, S. B. ;
Ivanovska, I. ;
Jonas, E. A. ;
Lee, S. J. ;
Chen, Y. ;
Kaczmarek, L. K. ;
Pineda, F. ;
Hardwick, J. M. .
ONCOGENE, 2006, 25 (34) :4697-4705
[6]   Potent cytotoxic lignans from Justicia procumbens and their effects on nitric oxide and tumor necrosis factor-α production in mouse macrophages [J].
Day, SH ;
Lin, YC ;
Tsai, ML ;
Tsao, LT ;
Ko, HH ;
Chung, MI ;
Lee, JC ;
Wang, JP ;
Won, SJ ;
Lin, CN .
JOURNAL OF NATURAL PRODUCTS, 2002, 65 (03) :379-381
[7]   Free radicals in the physiological control of cell function [J].
Dröge, W .
PHYSIOLOGICAL REVIEWS, 2002, 82 (01) :47-95
[8]   Mammalian caspases: Structure, activation, substrates, and functions during apoptosis [J].
Earnshaw, WC ;
Martins, LM ;
Kaufmann, SH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :383-424
[9]   ANTITUMOR AGENTS .81. JUSTICIDIN-A AND DIPHYLLIN, 2 CYTOTOXIC PRINCIPLES FROM JUSTICIA-PROCUMBENS [J].
FUKAMIYA, N ;
LEE, KH .
JOURNAL OF NATURAL PRODUCTS, 1986, 49 (02) :348-350
[10]   Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312