Department of Internal Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
College of Biology, Hunan University, Changsha, China.
Cancer Med. 2018 Dec;7(12):6158-6169. doi: 10.1002/cam4.1769. Epub 2018 Nov 6.
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.
纯化牡荆素化合物 1(VB1,一种从中药牡荆的种子中分离和提取的新木脂素)是一种有效的抗肿瘤剂,对包括结直肠癌在内的各种癌症表现出有希望的临床活性。然而,VB1 的抗肿瘤作用的确切潜在机制以及它如何引发癌细胞凋亡仍不清楚。在这里,我们证明 VB1 通过 p53 依赖性诱导 p53 上调凋亡调节剂(PUMA)促进凋亡,进而在结肠癌细胞 HCT-116 和 LoVo 中诱导 Bax(Bcl-2 相关 X 蛋白)激活和线粒体功能障碍。p53、PUMA 或 Bax 的缺乏会阻断 VB1 诱导的凋亡,并促进 HCT-116 细胞的存活。此外,VB1 与化疗药物 5-氟尿嘧啶(5-FU)或 NVP-BZE235 联合使用可通过诱导 HCT-116 细胞中的 PUMA 产生协同抗肿瘤作用。VB1 显著抑制了体外野生型(WT)HCT-116 和 LoVo 细胞的增殖和体内肿瘤的生长。结果表明,p53/PUMA/Bax 轴在 VB1 诱导的凋亡中起关键作用,VB1 作为一种新型抗癌药物,单独或与其他化疗药物联合使用,可能具有重要的临床应用价值。