The Chinese Herb Isolate Isorhapontigenin Induces Apoptosis in Human Cancer Cells by Down-regulating Overexpression of Antiapoptotic Protein XIAP

被引:60
作者
Fang, Yong [1 ,2 ]
Yu, Yonghui [1 ]
Hou, Qi [3 ,4 ]
Zheng, Xiao [1 ]
Zhang, Min [1 ]
Zhang, Dongyun [1 ]
Li, Jingxia [1 ]
Wu, Xue-Ru [5 ,6 ]
Huang, Chuanshu [1 ]
机构
[1] NYU, Sch Med, Nelson Inst Environm Med, Tuxedo Pk, NY 10987 USA
[2] Zhejiang Univ, Sir Run Run Shaw Hosp, Dept Med Oncol, Hangzhou 310016, Zhejiang, Peoples R China
[3] Mat Med Chinese Acad Med Sci, Beijing 100050, Peoples R China
[4] Peking Union Med Coll, Beijing 100050, Peoples R China
[5] NYU, Sch Med, Dept Urol, New York, NY 10016 USA
[6] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
X-LINKED INHIBITOR; TRAIL-MEDIATED APOPTOSIS; NUCLEAR-FACTOR; GENE PROMOTER; IN-VITRO; EXPRESSION; INDUCTION; ARSENITE; SP1; PROLIFERATION;
D O I
10.1074/jbc.M112.389494
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
Although the Chinese herb Gnetum cleistostachyum has been used as a remedy for cancers for hundred years, the active compounds and molecular mechanisms underlying its anti-cancer activity have not been explored. Recently a new derivative of stilbene compound, isorhapontigenin (ISO), was isolated from this Chinese herb. In the present study, we examined the potential of ISO in anti-cancer activity and the mechanisms involved in human cancer cell lines. We found that ISO exhibited significant inhibitory effects on human bladder cancer cell growth that was accompanied by marked apoptotic induction as well as down-regulation of the X-linked inhibitor of apoptosis protein (XIAP). Further studies have shown that ISO down-regulation of XIAP protein expression was only observed in endogenous XIAP, but not in constitutionally exogenously expressed XIAP in the same cells, excluding the possibility of ISO regulating XIAP expression at the level of protein degradation. We also identified that ISO down-regulated XIAP gene transcription via inhibition of Sp1 transactivation. There was no significant effect of ISO on apoptosis and colony formation of cells transfected with exogenous HA-tagged XIAP. Collectively, current studies, for the first time to the best of our knowledge, identify ISO as a major active compound for the anti-cancer activity of G. cleistostachyum by down-regulation of XIAP expression and induction of apoptosis through specific targeting of a SP1 pathway, and cast new light on the treatment of the cancer patients with XIAP overexpression.
引用
收藏
页码:35234 / 35243
页数:10
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