Purified vitexin compound 1, a new neolignan isolated compound, promotes PUMA-dependent apoptosis in colorectal cancer

被引:21
作者
Chen, Jingfei [1 ,2 ,3 ,4 ]
Zhong, Juchang [2 ]
Liu, Yeying [1 ]
Huang, Yuan [2 ]
Luo, Fei [5 ]
Zhou, Yingjun [6 ]
Pan, Xi [7 ]
Cao, Shousong [8 ]
Zhang, Lingling [3 ]
Zhang, Yingjie [2 ,9 ]
Wang, Jangang [1 ]
机构
[1] Cent South Univ, Xiangya Hosp 3, Dept Internal Med, Changsha, Hunan, Peoples R China
[2] Hunan Univ, Coll Biol, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Sch Med, Dept Lab Med, Changsha, Hunan, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Dept Obstet & Gynecol, Changsha, Hunan, Peoples R China
[5] Second Xiangya Hosp, Dept Cardiol, Changsha, Hunan, Peoples R China
[6] Cent South Univ, Sch Pharmaceut Sci, Changsha, Hunan, Peoples R China
[7] Cent South Univ, Xiangya Hosp 3, Dept Oncol, Changsha, Hunan, Peoples R China
[8] Southwest Med Univ, Sch Pharm, Dept Pharmacol, Luzhou, Peoples R China
[9] Hunan Univ, Shenzhen Inst, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; Bcl-2-associated X protein; colorectal cancer; p53; PUMA; vitexin compound 1; NF-KAPPA-B; BCL-X-L; CELL-DEATH; INDUCE APOPTOSIS; FAMILY; INHIBITION; ACTIVATION; EXPRESSION; PROTEINS; LIGNANS;
D O I
10.1002/cam4.1769
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purified vitexin compound 1 (VB1, a neolignan isolated and extracted from the seed of Chinese herb Vitex negundo) is an effective antitumor agent and exhibits promising clinical activity against various cancers including colorectal cancer. However, it remains unknown about the precise underlying mechanism associated with the antitumor effect of VB1 and how it triggers apoptosis in cancer cells. Here, we demonstrated that VB1 promoted apoptosis via p53-dependent induction of p53 upregulated modulator of apoptosis (PUMA) and further to induce Bax (Bcl-2-associated X protein) activation and mitochondrial dysfunction in colon cancer HCT-116 and LoVo cells. Deficiency in p53, PUMA, or Bax abrogated VB1-induced apoptosis and promoted cell survival in HCT-116 cells. Furthermore, the combination of VB1 with chemotherapeutic drugs 5-fluorouracil (5-FU) or NVP-BZE235 resulted in a synergistic antitumor effect via PUMA induction in HCT-116 cells. VB1 significantly suppressed the cell proliferation of wild-type (WT) HCT-116 and LoVo cells in vitro and tumor growth in vivo. The results indicate that p53/PUMA/Bax axis plays a critical role in VB1-induced apoptosis and VB1 may have valuable clinical applications in cancer therapy as a novel anticancer agent used alone or in combination with other chemotherapeutic drugs.
引用
收藏
页码:6158 / 6169
页数:12
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