Mi Yuan, Li Xuzhe, Wang Cong, Lin Chenxi, Zhao Zhichao, Yan Xiaofei, Shi Ping, Wang Lei
( 050017) Department of Emergency, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050017, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2024 Sep 20;55(5):1202-1209. doi: 10.12182/20240960505.
To investigate the effect of miR-2110 on the biological behaviors, such as cell proliferation, apoptosis, and metastasis, of lung adenocarcinoma (LUAD) cells by means of cell and animal experiments.
Bioinformatics websites, including ENCORI, TargetScan, miRTarBase, and Tarbase, were used to analyze the changes in the expression of miR-2110 in LUAD samples and to predict miR-2110 target. LUAD tissue samples and cells were collected and the changes in the expression of miR-2110 were verified through PCR technology. CCK-8 assay, clonogenic assay, Transwell assay, and flow cytometry were conducted to analyze alterations in the functions of LUAD cells. In addition, 10 BALB/c female nude mice aged 6 to 8 weeks were randomly divided into 2 groups, and the effect of miR-2110 on LUAD was investigated by experiments.
miR-2110 was significantly decreased in LUAD tissues and cells compared with the normal lung tissues. miR-2110 overexpression inhibited the proliferation and metastasis of LUAD cells and promoted the apoptosis of tumor cells (<0.05). Bioinformatics prediction and dual luciferase reporter gene assay results confirmed that miR-2110 could target and bind to CDT1. In addition, overexpression of gene reversed the proliferation, metastasis, and apoptosis of miR-2110 compared with the miR-2110 overexpression group (<0.05). Nude mice experiments showed that miR-2110 overexpression significantly decreased the expression of Ki67, a tumor proliferation index, and vimentin and MMP9, two metastasis indices, compared with the control group.
miR-2110 can inhibit proliferation and metastasis of LUAD by targeting CDT1, providing a new rationale for the treatment of LUAD.
通过细胞和动物实验研究miR-2110对肺腺癌(LUAD)细胞增殖、凋亡和转移等生物学行为的影响。
利用包括ENCORI、TargetScan、miRTarBase和Tarbase在内的生物信息学网站分析LUAD样本中miR-2110的表达变化并预测miR-2110靶点。收集LUAD组织样本和细胞,通过PCR技术验证miR-2110表达的变化。进行CCK-8检测、克隆形成检测、Transwell检测和流式细胞术分析LUAD细胞功能的改变。此外,将10只6至8周龄的雌性BALB/c裸鼠随机分为2组,通过实验研究miR-2110对LUAD的影响。
与正常肺组织相比,LUAD组织和细胞中miR-2110显著降低。miR-2110过表达抑制LUAD细胞的增殖和转移并促进肿瘤细胞凋亡(P<0.05)。生物信息学预测和双荧光素酶报告基因检测结果证实miR-2110可靶向并结合CDT1。此外,与miR-2110过表达组相比,CDT1基因过表达逆转了miR-2110的增殖、转移和凋亡作用(P<0.05)。裸鼠实验表明,与对照组相比,miR-2110过表达显著降低肿瘤增殖指数Ki67以及转移指标波形蛋白和基质金属蛋白酶9的表达。
miR-2110可通过靶向CDT1抑制LUAD的增殖和转移,为LUAD的治疗提供了新的理论依据。