细胞凋亡
体内
细胞生长
癌症研究
细胞周期
肺癌
细胞
A549电池
细胞培养
体外
程序性细胞死亡
医学
药理学
生物
肿瘤科
生物化学
遗传学
生物技术
作者
Zongyi Shen,Liqi Yin,Manxia Chang,Haifeng Wang,Mingxuan Hao,Youfeng Liang,Rui Guo,Ying Bi,Jiansong Wang,Changyuan Yu,Jinmei Li,Qiong-Li Zhai,Run-Fen Cheng,Jinku Zhang,Jirui Sun,Zhao Yang
出处
期刊:Acta Pharmaceutica
[De Gruyter]
日期:2024-03-01
卷期号:74 (1): 149-164
被引量:1
标识
DOI:10.2478/acph-2024-0006
摘要
Abstract Lung cancer (LC) is the leading cause of cancer deaths worldwide. Surgery, chemoradiotherapy, targeted therapy, and immunotherapy are considered dominant treatment strategies for LC in the clinic. However, drug resistance and meta-stasis are two major challenges in cancer therapies. Medicarpin (MED) is an isoflavone compound isolated from alfalfa, which is usually used in traditional medicine. This study was de sig ned to evaluate the anti-LC effect and reveal the underlying mechanisms of MED in vivo and in vitro . We found that MED could significantly inhibit proliferation, induce apoptosis, and cell cycle arrest of A549 and H157 cell lines. Basically, MED induced cell apoptosis of LC cells by upregu lating the expression of pro-apoptotic proteins BAX and Bak1, leading to the cleavage of caspase-3 (Casp3). Moreover, MED inhibited the proliferation of LC cells via downregulating the expression of proliferative protein Bid. Overall, MED inhibited LC cell growth in vitro and in vivo via suppressing cell proliferation and inducing cell apoptosis, suggesting the therapeutic potential of MED in treating LC.
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