Effect and mechanism of CyPA in radiosensitization of lung adenocarcinoma using CRISPR/Cas9 technology

Cypa 辐射敏感性 癌症研究 细胞凋亡 条件基因敲除 医学 药理学 化学 免疫学 内科学 放射治疗 生物化学 基因 表型 人类免疫缺陷病毒(HIV)
作者
Jinkun Ma,Lin Xu,Jinchang Huang,Qiaoli Zhang,Yuqin Qiu,Xuewei Qi,Lina Wang,Yuchan Cao,Бо Лю,Shiyun Liu
出处
期刊:Journal of Traditional Chinese Medical Sciences [Elsevier BV]
卷期号:7 (1): 53-58
标识
DOI:10.1016/j.jtcms.2020.01.006
摘要

To explore the role of cyclophilin A (CyPA) in sensitization of lung adenocarcinoma to radiotherapy using CRISPR/Cas9 technology. A CyPA knockout human lung adenocarcinoma cell line H1975 was established by CRISPR/Cas9 technology. Groups included a control group (wildtype), CyPA knockout group, traditional Chinese medicine (TCM) extract with Fuzhengzengxiao decoction group, and TCM extract with Fuzhengzengxiao decoction + CyPA knockout group. Each group was exposed to radiation at doses of 0, 2, 4, 6, and 8 Gy. After 24 h, MTT assays were used to determine the survival rate of lung cancer cells and calculate radiosensitivity. The qPCR was used to measure mRNA expression of DDIT3, CDKN1A, and CDC25A associated with DNA damage repair. Without irradiation, Fuzhengzengxiao decoction reduced the survival rate of lung adenocarcinoma cells (P < .0001). After irradiation, TCM extract with Fuzhengzengxiao decoction, CyPA knockout, and TCM extract with Fuzhengzengxiao decoction + CyPA knockout groups had reduced survival rates (P < .0001) and radiosensitivity was increased significantly. Expression of DDIT3, CDKN1A, and CDC25A was upregulated after knockout of CyPA (P < .0001). Expression of DDIT3 and CDC25A was increased after irradiation in wildtype cells treated with TCM extract with Fuzhengzengxiao decoction (DDIT3, P < .0001; CDC25A, P = .0059). The TCM extract with Fuzhengzengxiao decoction + CyPA knockout group also had increased expression of DDIT3 and CDC25A after irradiation (P < .0001). Fuzhengzengxiao decoction significantly decreases the survival rate of lung cancer cells, and its mechanism may be related to radiosensitization by decreasing expression of CyPA and inducing G1/S cell cycle arrest.
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