机构：[1]Section Pathology of The Institute of Forensic Medicine, University Hospital Jena, Friedrich Schiller University, D‑07747 Jena[2]Leibniz Institute on Ageing‑Fritz Lipmann Institute (FLI), D‑07745 Jena, Germany[3]School of Medicine (Shenzhen), Sun Yat‑Sen University, Guangzhou, Guangdong 510006, P.R. China[4]Institute of Pathology, SRH Wald‑Klinikum, D‑07548 Gera, Germany[5]School of Ethnic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 611137, P.R. China
Mutations of p53 occur in approximately 50% of advanced non‑small cell lung cancer (NSCLC) cases, leading to loss of tumor suppressive function and/or gain of p53 oncogenic activity. Reactivation of mutant p53 and consequently induction of apoptosis in cancer cells is the goal of p53‑targeted therapy. Recently, several p53 mutant reactivating compounds were discovered including SCH 529074. However, the role of SCH 529074 in NSCLC has not been fully explored. In the present study, the effects of this compound on cell survival, cell cycle progression, induction of apoptosis and modulation of cell signaling in p53 mutant NSCLC cells (H1975, H322 and H157) and p53 wild‑type NSCLC cells (A549), was investigated. Cell‑based functional assays, real‑time RT‑qPCR and western blot assays were used. HCT116 [p53 wild‑type (WT)] and HCT116 p53‑/‑ (p53 null) were used as control cells. The results demonstrated that SCH 529074 treatment caused significant reduction in cell viability and colony formation activity in p53 mutant, p53 WT and p53‑deficient cells. The treatment of NSCLC cells with SCH 529074 resulted in a dose‑dependent induction of apoptosis and G0/G1 cell cycle arrest, which was associated with the activation of caspases (3 and 7), p53‑independent upregulation of p21 and PUMA as well as increased LC3II, a biomarker of autophagy. The combination treatment with the autophagy inhibitor chloroquine (CQ) and SCH 529074 led to decreased cell viability, colony formation and increased induction of apoptosis. The data indicated that SCH 529074 may exert its growth inhibitory function in a p53‑independent manner in NSCLC cells.
基金：
The present study was supported by University Hospital Jena.
语种：
外文
PubmedID：
中科院(CAS)分区：
出版当年[2020]版：
大类|3 区医学
小类|3 区肿瘤学
最新[2023]版：
大类|3 区医学
小类|4 区肿瘤学
第一作者：
第一作者机构：[1]Section Pathology of The Institute of Forensic Medicine, University Hospital Jena, Friedrich Schiller University, D‑07747 Jena
通讯作者：
通讯机构：[1]Section Pathology of The Institute of Forensic Medicine, University Hospital Jena, Friedrich Schiller University, D‑07747 Jena[*1]Section Pathology of The Institute of Forensic Medicine, University Hospital Jena, Friedrich Schiller University, Am Klinikum 1, D‑07747 Jena, Germany
推荐引用方式(GB/T 7714)：
MILJANA NENKOV,YUNXIA MA,DANIELA HAASE,et al.Growth inhibitory role of the p53 activator SCH 529074 in non‑small cell lung cancer cells expressing mutant p53.[J].Oncology reports.2020,43(6):2073-2082.doi:10.3892/or.2020.7546.
APA：
MILJANA NENKOV,YUNXIA MA,DANIELA HAASE,ZHONGWEI ZHOU,YONG LI...&YUAN CHEN.(2020).Growth inhibitory role of the p53 activator SCH 529074 in non‑small cell lung cancer cells expressing mutant p53..Oncology reports,43,(6)
MLA：
MILJANA NENKOV,et al."Growth inhibitory role of the p53 activator SCH 529074 in non‑small cell lung cancer cells expressing mutant p53.".Oncology reports 43..6(2020):2073-2082
