Feng Jing, Li Shan, Li Laihua, Du Zhiqiang, Yang Guangying, Zhao Zhi, Fan Xueke, Wang Na, Zhao Zhigang
Zhengzhou Yihe Hospital Affiliated to Henan University, Zhengzhou, Henan Province, China.
Henan University of Chinese Medicine, Zhengzhou, Henan Province, China.
J Cell Mol Med. 2025 Jun;29(11):e70610. doi: 10.1111/jcmm.70610.
AMBRA1 is associated with a variety of pathological processes in cancer cells, but may have different functions in different tumour microenvironments or genetic backgrounds. In this study, the function and regulatory mechanisms of AMBRA1 were explored in the progression of non-small cell lung cancer (NSCLC). The abnormally expressed miRNAs in AMBRA1-overexpressed and differentially expressed genes in miR-1178-knockdown NSCLC cells were validated by RNA sequencing. Cell viability, proliferation, invasion, apoptosis, and cell cycle were tested through Cell Counting Kit-8 (CCK-8), EdU, colony formation, transwell, and flow cytometry. A mouse tumour xenograft model was conducted to assess the roles of the AMBRA1-miR-1178 axis on NSCLC progression in vivo. AMBRA1 overexpression suppressed NSCLC cell proliferation and invasion, while promoting apoptosis and G0/G1 phase cell cycle arrest in vitro, and inhibited tumour growth in vivo. RNA sequencing revealed miR-1178 as a target of AMBRA1. miR-1178 overexpression partially weakened the suppressive function of AMBRA1 on cell malignant biological behaviours. p53 and CDK2 were confirmed as the downstream targets of miR-1178. Silencing p53 or overexpressing CDK2 reversed the repressive effects of AMBRA1 on the development of NSCLC cells. AMBRA1 may suppress the malignant phenotype of NSCLC cells via regulating the miR-1178-p53-CDK2 signalling pathway.
AMBRA1与癌细胞中的多种病理过程相关,但在不同的肿瘤微环境或基因背景中可能具有不同的功能。在本研究中,探讨了AMBRA1在非小细胞肺癌(NSCLC)进展中的功能及调控机制。通过RNA测序验证了AMBRA1过表达的非小细胞肺癌细胞中异常表达的miRNA以及miR-1178敲低后差异表达的基因。通过细胞计数试剂盒-8(CCK-8)、EdU、集落形成、Transwell和流式细胞术检测细胞活力、增殖、侵袭、凋亡和细胞周期。建立小鼠肿瘤异种移植模型以评估AMBRA1-miR-1178轴在体内对非小细胞肺癌进展的作用。AMBRA1过表达在体外抑制非小细胞肺癌细胞增殖和侵袭,同时促进凋亡和G0/G1期细胞周期阻滞,并在体内抑制肿瘤生长。RNA测序显示miR-1178是AMBRA1的靶标。miR-1178过表达部分削弱了AMBRA1对细胞恶性生物学行为的抑制功能。p53和CDK2被确认为miR-1178的下游靶标。沉默p53或过表达CDK2可逆转AMBRA1对非小细胞肺癌细胞发育的抑制作用。AMBRA1可能通过调节miR-1178-p53-CDK2信号通路抑制非小细胞肺癌细胞的恶性表型。