Ye Longping, Zhong Youqing, Hu Lihua, Huang Ya, Tang Xiang, Yu Shanjun, Huang Jianxin, Wang Ziyuan, Li Qi, Zhou Xiangdong
Department of Respiratory Medicine, The First Affiliated Hospital of Hainan Medical University, Haikou, Hainan 570102, China.
NHC Key Laboratory of Tropical Disease Control, Hainan Medical University, Haikou 571199, China.
Oxid Med Cell Longev. 2022 Sep 16;2022:4509019. doi: 10.1155/2022/4509019. eCollection 2022.
This study was aimed at investigating the expression level of hsa_circ_0061817 in lung adenocarcinoma cells and its effect on cell proliferation and invasion and the possible mechanism of hsa_circ_0061817 in lung adenocarcinoma.
The overexpression plasmids of hsa_circ_0061817 (OE-hsacirc_0061817) were transfected into human lung A549 cells and mouse LLC-LUC cells, respectively. The cell viability was detected by CCK-8, and the cell proliferation was detected by cell clone formation assay and EdU assay. Transwell test was used to detect the ability of cell invasion, and apoptosis was detected by flow cytometry. WB was applied to determine the expression of apoptosis and epithelial mesenchymal transition- (EMT-) related proteins and also target proteins for observation the effect of OE-hsa_circ_0061817 on the growth of A549 cells in nude mice. Bioinformatics method was used to predict the binding microRNA (miRNA) of hsa_circ_0061817 and construct the regulatory network of competitive endogenous RNA (ceRNA) and functional analysis of miRNA target genes.
Compared with PLO-ciR group, the cell viability, proliferation, and invasive ability of A549 and LLC-LUC were significantly reduced in OE-hsa_circ_00061817 group, while the apoptosis increased in OE-hsa_circ_00061817 group compared to PLO-ciR group. WB results showed that the expression of caspase 3, caspase 7, caspase 9, and E-cadherin increased significantly, while the expression levels of vimentin and N-cadherin decreased severely. Most importantly, OE-hsa_circ_00061817 inhibited the growth of A549 tumor-bearing nude mice. According to TargetScan and mirBase databases, hsa_circ_0061817 may competitively bind hsa_mir-181b-3p, hsa-mir-337-3p, hsa-mir-421, and hsa-mir-548d-3p. The results of functional enrichment showed that miRNA target genes were involved in many cancer-related biological processes, including negative regulation of apoptosis, gene expression, transcriptional imbalance in cancer, transforming growth factor-, and P53 signal pathway.
Over expression of hsa_circ_0061817 inhibits the proliferation of lung adenocarcinoma A549 and LLC-LUC cells and may reduce the invasive ability of lung adenocarcinoma cells by weakening the process of EMT, which provides a new target for the prevention and treatment of lung adenocarcinoma.
本研究旨在探讨hsa_circ_0061817在肺腺癌细胞中的表达水平及其对细胞增殖和侵袭的影响,以及hsa_circ_0061817在肺腺癌中的可能作用机制。
将hsa_circ_0061817的过表达质粒(OE-hsacirc_0061817)分别转染到人肺A549细胞和小鼠LLC-LUC细胞中。采用CCK-8法检测细胞活力,通过细胞克隆形成实验和EdU实验检测细胞增殖情况。运用Transwell实验检测细胞侵袭能力,采用流式细胞术检测细胞凋亡情况。应用蛋白质免疫印迹法(WB)检测凋亡及上皮间质转化(EMT)相关蛋白的表达,以及观察OE-hsa_circ_0061817对裸鼠体内A549细胞生长影响的靶蛋白。采用生物信息学方法预测hsa_circ_0061817结合的微小RNA(miRNA),构建竞争性内源RNA(ceRNA)调控网络并对miRNA靶基因进行功能分析。
与PLO-ciR组相比,OE-hsa_circ_00061817组A549和LLC-LUC细胞的活力、增殖和侵袭能力显著降低,而OE-hsa_circ_00061817组细胞凋亡率高于PLO-ciR组。WB结果显示,caspase 3、caspase 7、caspase 9和E-钙黏蛋白的表达显著增加,而波形蛋白和N-钙黏蛋白的表达水平严重降低。最重要的是,OE-hsa_circ_00061817抑制了A549荷瘤裸鼠的生长。根据TargetScan和mirBase数据库,hsa_circ_0061817可能竞争性结合hsa_mir-181b-3p、hsa-mir-337-3p、hsa-mir-421和hsa-mir-548d-3p。功能富集结果表明,miRNA靶基因参与许多癌症相关的生物学过程,包括凋亡的负调控、基因表达、癌症中的转录失衡、转化生长因子和P53信号通路。
hsa_circ_0061817的过表达抑制了肺腺癌A549和LLC-LUC细胞的增殖,并可能通过减弱EMT过程降低肺腺癌细胞的侵袭能力,为肺腺癌的防治提供了新的靶点。