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

机译:提纯的葡萄胎蛋白化合物1(一种新的新木脂素分离的化合物)促进大肠癌中PUMA依赖性细胞凋亡

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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.
机译:纯化的牡荆素化合物1(VB1,是一种从中草药荆棘的种子中提取并提取的新木脂素)是一种有效的抗肿瘤剂,并且对包括结肠直肠癌在内的多种癌症均显示出有希望的临床活性。然而,与VB1的抗肿瘤作用有关的确切的潜在机制以及它如何触发癌细胞的凋亡仍然未知。在这里,我们证明了VB1通过p53依赖性诱导p53上调的细胞凋亡调节剂(PUMA)促进了细胞凋亡,并进一步诱导了结肠癌HCT-116和LoVo细胞中的Bax(Bcl-2相关X蛋白)活化和线粒体功能障碍。 p53,PUMA或Bax的缺乏消除了VB1诱导的凋亡,并促进了HCT-116细胞的细胞存活。此外,VB1与化学治疗药物5-氟尿嘧啶(5-FU)或NVP-BZE235的组合通过HCT-116细胞中的PUMA诱导产生协同抗肿瘤作用。 VB1在体外显着抑制野生型(WT)HCT-116和LoVo细胞的细胞增殖,并在体内抑制肿瘤的生长。结果表明,p53 / PUMA / Bax轴在VB1诱导的细胞凋亡中起着至关重要的作用,VB1作为一种单独或与其他化疗药物结合使用的新型抗癌剂,在癌症治疗中可能具有重要的临床应用。

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