柴胡皂苷-b2 通过靶向 MACC1/c-Met/Akt 信号通路调控肝癌细胞的增殖和凋亡

IF 2.1 Q3 PHARMACOLOGY & PHARMACY Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.1155/2024/2653426
Yanxue Zhu, Xingzhi Lv, Ruifang Li, Zihan Gao, Chanhao Lei, Lan Wang, Sanqiang Li
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引用次数: 0

摘要

柴胡皂苷-b2(SS-b2)是从柴胡根中提取的一种活性成分,具有抗肿瘤、抗炎、抗氧化和保肝作用。我们研究了 SS-b2 在 HepG2 肝癌细胞和 H22 肿瘤小鼠体内对肿瘤增殖的抑制作用及其分子机制,包括 MACC1/p-c-Met/p-Akt 通路的表达。动物实验表明,SS-b2 能显著降低移植了 H22 肝癌细胞的小鼠肿瘤组织中 MACC1、p-c-MET 和 p-Akt 的水平,同时增加 p-BAD 的表达。结果还显示,与对照组相比,SS-b2 治疗组的 MACC1、p-c-MET 和 p-Akt 表达受到浓度依赖性抑制。此外,SS-b2 对 MACC1 活化的抑制导致了 HepG2 肝癌细胞活力和增殖的降低,这种降低与多柔比星(DOX)的效果相当。这表明 SS-b2 对肝癌有显著疗效,可与 DOX 相媲美。同时,Annexin V-FITC/PI 染色和蛋白印迹分析表明,SS-b2 可诱导 HepG2 肝癌细胞凋亡。这些发现提供了实验证据,表明 SS-b2 是一种很有前景的肝癌抗癌剂。
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Saikosaponin-b2 Regulates the Proliferation and Apoptosis of Liver Cancer Cells by Targeting the MACC1/c-Met/Akt Signalling Pathway.

Saikosaponin-b2 (SS-b2), an active ingredient derived from the root of Radix Bupleuri, possesses antitumour, anti-inflammatory, antioxidative and hepatoprotective properties. We investigated the inhibition of tumour proliferation by SS-b2 and the underlying molecular mechanisms, including the MACC1/p-c-Met/p-Akt pathway expression in HepG2 liver cancer cells and H22 tumour-bearing mice. Animal experiments showed that SS-b2 significantly decreased the levels of MACC1, p-c-MET and p-Akt in tumour tissue transplanted with H22 liver cancer cells in mice, while it increased the expression of p-BAD. The results also revealed a concentration-dependent suppression of MACC1, p-c-Met and p-Akt expression in the SS-b2 treatment group compared with the control group. Additionally, the suppression of MACC1 activation by SS-b2 resulted in a reduction in the viability and proliferation of HepG2 liver cancer cells, and this reduction was comparable to that by doxorubicin (DOX). This suggests that SS-b2 has significant efficacy in liver cancer, comparable to DOX. Meanwhile, Annexin V-FITC/PI staining and western blot analysis of cleaved caspase 9 and cleaved caspase 3 demonstrated that SS-b2 induced apoptosis of HepG2 liver cancer cells. These findings provide experimental evidence suggesting that SS-b2 is a promising anticancer agent for liver cancer.

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来源期刊
CiteScore
4.30
自引率
3.60%
发文量
0
审稿时长
17 weeks
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