Medicarpin suppresses lung cancer cell growth in vitro and in vivo by inducing cell apoptosis

Author:

Shen Zongyi1,Yin Liqi1,Chang Manxia1,Wang Haifeng2,Hao Mingxuan1,Liang Youfeng1,Guo Rui1,Bi Ying1,Wang Jiansong2,Yu Changyuan1,Li Jinmei34,Zhai Qiongli5,Cheng Runfen5,Zhang Jinku34,Sun Jirui34ORCID,Yang Zhao16ORCID

Affiliation:

1. College of Life Science and Technology, Innovation Center of Molecular Diagnostics , Beijing University of Chemical Technology , , China

2. Department of Urology, The Second Affiliated Hospital of Kunming Medical University , , China

3. Department of Pathology , Baoding No. 1 Central Hospital , , Hebei , China

4. Key Laboratory of Molecular Pathology and Early Diagnosis of Tumor in Hebei Province , , Hebei , China

5. Department of Pathology, National Clinical Research Center of Cancer, Key Laboratory of Cancer Prevention and Therapy , Tianjin Medical University Cancer Institute and Hospital , , China

6. College of Life Science and Technology, Key Laboratory of Protection and Utilization of Biological Resources in Tarim Basin of Xinjiang Production and Construction Corps , Tarim University , , China

Abstract

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.

Publisher

Walter de Gruyter GmbH

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