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苯乙醇苷诱导肝癌细胞凋亡通过线粒体依赖性和 MAPK 途径,并通过与顺铂联合增强抗肿瘤作用。

Phenylethanoid Glycosides Induce Apoptosis of Hepatocellular Carcinoma Cells by Mitochondria-Dependent and MAPK Pathways and Enhance Antitumor Effect through Combination with Cisplatin.

机构信息

Xinjiang University, Urumqi, Xinjiang, China.

出版信息

Integr Cancer Ther. 2021 Jan-Dec;20:15347354211013085. doi: 10.1177/15347354211013085.

Abstract

is a type of Chinese herbal medicine and exerts various biological functions. Previous studies have been demonstrated that phenylethanoid glycosides (CTPG) exhibit antitumor effects on a variety of tumor cells. However, the antitumor effects of CTPG on HepG2 and BEL-7404 hepatocellular carcinoma (HCC) cells are still elusive. Our study showed that CTPG significantly inhibited the growth of HepG2 and BEL-7404 cells through the induction of cell cycle arrest and apoptosis, which was associated with the activation of MAPK pathways characterized by the up-regulated phosphorylation of p38, JNK, and ERK1/2 and mitochondria-dependent pathway characterized by the reduction of mitochondrial membrane potential. The release of cytochrome and the cleavage of caspase-3, -7, -9, and PARP were subsequently increased by CTPG treatment. Moreover, CTPG significantly suppressed the migration of HepG2 through reducing the levels of matrix metalloproteinase-2 and vascular endothelial growth factor. Interestingly, CTPG not only enhanced the proliferation of splenocytes but also reduced the apoptosis of splenocytes induced by cisplatin. In H22 tumor mouse model, CTPG combined with cisplatin further inhibited the growth of H22 cells and reduced the side effects of cisplatin. Taken together, CTPG inhibited the growth of HCC through direct antitumor effect and indirect immunoenhancement effect, and improved the antitumor efficacy of cisplatin.

摘要

是一种中草药,具有多种生物功能。先前的研究表明,苯乙醇苷(CTPG)对多种肿瘤细胞具有抗肿瘤作用。然而,CTPG 对 HepG2 和 BEL-7404 肝癌(HCC)细胞的抗肿瘤作用仍不清楚。我们的研究表明,CTPG 通过诱导细胞周期停滞和细胞凋亡显著抑制 HepG2 和 BEL-7404 细胞的生长,这与 MAPK 途径的激活有关,其特征是 p38、JNK 和 ERK1/2 的磷酸化上调和线粒体依赖性途径有关,其特征是线粒体膜电位降低。随后,CTPG 处理后细胞色素 c 的释放和 caspase-3、-7、-9 和 PARP 的裂解增加。此外,CTPG 通过降低基质金属蛋白酶-2 和血管内皮生长因子的水平显著抑制 HepG2 的迁移。有趣的是,CTPG 不仅增强了脾细胞的增殖,而且减少了顺铂诱导的脾细胞凋亡。在 H22 肿瘤小鼠模型中,CTPG 与顺铂联合进一步抑制了 H22 细胞的生长,并降低了顺铂的副作用。总之,CTPG 通过直接抗肿瘤作用和间接免疫增强作用抑制 HCC 的生长,提高了顺铂的抗肿瘤疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8b/8113936/ac19e395da6f/10.1177_15347354211013085-img2.jpg

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