Sun Piyun, Feng Yuchen, Guo Hui, Li Rong, Yu Peng, Zhou Xingguang, Pan Zhige, Liang Yanyan, Yu Bihan, Zheng Yanyi, Shi Yu, Wen Lingbo, Wei Minmei, Chen Yanhua
Department of Oncology, Liuzhou Hospital of Traditional Chinese Medicine, Liuzhou City, Guangxi Province 545001, People's Republic of China.
Cancer Manag Res. 2020 Jun 22;12:4799-4806. doi: 10.2147/CMAR.S245520. eCollection 2020.
MCM3AP-AS1 has been characterized as an oncogenic lncRNA in several types of cancer, while its role in nasopharyngeal carcinoma (NPC) is unknown. This study aimed to investigate the role of MCM3AP-AS1 in NPC.
Paired NPC tissues and non-tumor tissues were collected from 55 NPC patients. Expression of MCM3AP-AS1 and miR-34a in paired tissues was analyzed by RT-qPCR. Interactions between MCM3AP-AS1 and miR-34a were analyzed by overexpression experiments. The roles of MCM3AP-AS1 and miR-34a in regulating NPC cell proliferation and apoptosis were explored by cell proliferation assay and cell apoptosis assay, respectively.
Our bioinformatics analysis showed that MCM3AP-AS1 may be targeted by miR-34a, which is a well-studied tumor suppressor miRNA. In this study, we showed that miR-34a was downregulated and MCM3AP-AS1 was upregulated in NPC. An inverse correlation between the expression of MCM3AP-AS1 and miR-34a was found across NPC tissue samples. High expression level of MCM3AP-AS1 and low levels of miR-34a in NPC tissues predicted the poor survival. In NPC cells, overexpression of MCM3AP-AS1 did not affect the expression of miR34a, while overexpression of miR-34a led to downregulated MCM3AP-AS1. Cell proliferation and apoptosis assay showed that overexpression of miR-34a reduced the enhancing effects of overexpressing MCM3AP-AS1 on cell proliferation and the inhibitory effects on cell apoptosis.
MiR-34a inhibits cell proliferation and induces apoptosis in human NPC by targeting MCM3AP-AS1.
MCM3AP-AS1在多种癌症中被鉴定为致癌长链非编码RNA,但其在鼻咽癌(NPC)中的作用尚不清楚。本研究旨在探讨MCM3AP-AS1在NPC中的作用。
收集55例NPC患者的配对NPC组织和非肿瘤组织。采用RT-qPCR分析配对组织中MCM3AP-AS1和miR-34a的表达。通过过表达实验分析MCM3AP-AS1与miR-34a之间的相互作用。分别通过细胞增殖实验和细胞凋亡实验探讨MCM3AP-AS1和miR-34a在调节NPC细胞增殖和凋亡中的作用。
我们的生物信息学分析表明,MCM3AP-AS1可能是已被充分研究的肿瘤抑制性微小RNA(miRNA)miR-34a的靶标。在本研究中,我们发现NPC中miR-34a表达下调而MCM3AP-AS1表达上调。在NPC组织样本中发现MCM3AP-AS1与miR-34a的表达呈负相关。NPC组织中MCM3AP-AS1的高表达水平和miR-34a的低水平预示着预后不良。在NPC细胞中,MCM3AP-AS1的过表达不影响miR34a的表达,而miR-34a的过表达导致MCM3AP-AS1表达下调。细胞增殖和凋亡实验表明,miR-34a的过表达降低了MCM3AP-AS1过表达对细胞增殖的增强作用以及对细胞凋亡的抑制作用。
miR-34a通过靶向MCM3AP-AS1抑制人NPC细胞的增殖并诱导其凋亡。