基因敲除
信使核糖核酸
转移
生物
癌症研究
基因
癌症
遗传学
作者
Anbing Dong,Ming Gao,Xiangqian Zheng,Xianhui Ruan
出处
期刊:Endocrine, metabolic & immune disorders
[Bentham Science Publishers]
日期:2023-04-17
卷期号:23 (11): 1400-1409
被引量:1
标识
DOI:10.2174/1871530323666230417083509
摘要
This study was to investigate the clinical significance of miR-551b-5p and SETD2 in thyroid cancers (TC) and their effects on the biological function of TC cells.The expression level of miR-551b-5p and SETD2 in tumor/nontumor tissues and TC cell lines was measured by quantitative real-time polymerase chain reaction (RT-qPCR). Subsequently, the relationship between miR-551b-5p or SETD2 expression and the clinicopathological feature was detected by Chi-square analysis. Kaplan-Meier and multivariate Cox regression analyses were used to assess their prognostic values. Finally, the regulatory effects of miR-551b-5p and SETD2 on the proliferation, migration and invasion ability of TC cells were detected by CCK-8 and Transwell assays.Compared with non-tumor groups, the expression of miR-551b-5p was significantly increased in patients' tissues and TC cell lines, while SETD2 mRNA expression was decreased. Patients with up-regulated miR-551b-5p or downregulated SETD2 mRNA in TC showed more positive lymph node metastasis and advanced TNM stage. High miR-551b-5p expression level and low SETD2 mRNA level were related to poor survival rate. miR-551b-5p and SETD2 might be potential prognostic biomarkers for TC. miR-551b-5p knockdown can inhibit cell proliferation, migration and invasion by targeting SETD2.miR-551b-5p and SETD2 may be valuable prognostic biomarkers and new therapeutic targets for TC.
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