Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Department of Gynaecology and Obstetrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Cell Signal. 2022 Sep;97:110390. doi: 10.1016/j.cellsig.2022.110390. Epub 2022 Jun 18.
Plentiful evidence proves that lncRNAs play a crucial role in tumor development. However, the function and mechanism that were mediated by lncRNA HIF1A-AS2 in cervical cancer remain unclear.
The lncRNA HIF1A-AS2 was identified via high-throughput microarray analysis of three HPV 16-positive cervical squamous cell carcinoma (CSCC) samples and three HPV-negative normal controls. The expression of HIF1A-AS2 was detected by qRT-PCR in clinical tissues and cancer cells. In vitro and in vivo assays were performed through downregulation or upregulation of HIF1A-AS2. The possible mechanisms of HIF1A-AS2 in cervical cancer cells were explored by western blot, flow cytometric analysis and rescue assays.
HIF1A-AS2 was significantly increased in cervical cancer tissue, and in the HPV- positive cervical cancer cells. Further investigation showed that the inhibition of HIF1A-AS2 suppressed cell proliferation, migration, invasion, and induced apoptosis, while up-regulation of HIF1A-AS2 revealed opposite results. In terms of mechanism, we found that HIF1A-AS2 was mediated by HPV16 E6 and regulated cell apoptosis via P53/caspase 9/caspase 3 axis.
Our findings demonstrate that HIF1A-AS2 functions as a carcinogenic lncRNA that promotes tumor development, and serves as a candidate prognostic factor, which may contribute to the treatment of cervical cancer.
大量证据表明 lncRNA 在肿瘤发展中发挥着关键作用。然而,lncRNA HIF1A-AS2 在宫颈癌中发挥作用的机制尚不清楚。
通过高通量微阵列分析 3 例 HPV16 阳性宫颈鳞状细胞癌(CSCC)样本和 3 例 HPV 阴性正常对照,鉴定出 lncRNA HIF1A-AS2。采用 qRT-PCR 检测临床组织和癌细胞中 HIF1A-AS2 的表达。通过下调或上调 HIF1A-AS2 进行体外和体内实验。通过 Western blot、流式细胞术分析和挽救实验探讨 HIF1A-AS2 在宫颈癌细胞中的可能作用机制。
HIF1A-AS2 在宫颈癌组织和 HPV 阳性的宫颈癌细胞中显著增加。进一步研究表明,抑制 HIF1A-AS2 抑制细胞增殖、迁移和侵袭,并诱导细胞凋亡,而上调 HIF1A-AS2 则显示出相反的结果。在机制方面,我们发现 HIF1A-AS2 受 HPV16 E6 介导,并通过 P53/caspase 9/caspase 3 轴调节细胞凋亡。
我们的研究结果表明,HIF1A-AS2 作为一种致癌 lncRNA 促进肿瘤的发展,可作为候选预后因素,可能有助于宫颈癌的治疗。