MiR-144-3p inhibits the proliferation and metastasis of lung cancer A549 cells via targeting HGF

被引:7
|
作者
Fang, Guiju [1 ]
Zhang, Canhui [1 ]
Liu, Zhixin [1 ]
Peng, Zhiwen [1 ]
Tang, Meiyan [1 ]
Xue, Qing [1 ]
机构
[1] Ningde Normal Univ, Ningde Municipal Hosp, Dept Resp Med, Ningde 352100, Peoples R China
关键词
Molecular mechanism; Lung cancer; microRNA-144-3p; HGF; HEPATOCYTE GROWTH-FACTOR; CLINICAL-SIGNIFICANCE; DOWN-REGULATION; SCATTER-FACTOR; C-MET; INVASION; EXPRESSION; RECEPTOR; AXIS; CARCINOMA;
D O I
10.1186/s13019-022-01861-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: MicroRNAs have been confirmed as vital regulators in gene expression, which could affect multiple cancer cell biological behaviors. This study aims to elucidate the molecular mechanism of miR-144-3p in lung cancer cellular proliferation and metastasis. Methods: MiR-144-3p expression in lung cancer tissues and cell lines was detected by qRT-PCR. HGF was predicted as the target gene of miR-144-3p using TargetScan and dual luciferase reporter assay. Immunohistochemistry and qRT-PCR were used to explore the impacts of HCF on lung cancer tissues and cell lines. Impacts of miR-144-3p and HGF on cancer cellular proliferation, migration and invasion were elucidated by CCK-8, Flow cytometry, Transwell invasion and Wound-healing assay. Moreover, nude mouse xenograft model was established to evaluate the effects of miR-144-3p on lung cancer cells. Results: MiR-144-3p exhibited a reduction in both lung cancer tissues and cell lines. HGF was a direct target of miR-144-3p. In contrast to the miR-144-3p expression level, HGF showed a higher level in lung cancer tissues and cell lines. Overexpression miR-144-3p suppressed A549 and NCI-H1299 cell proliferation and metastasis, whereas this was reversed by HGF. MiR-144-3p exhibited an inhibitory effect on A549 cell-induced tumor growth of nude mice. Conclusions: This study reveals miR-144-3p/HGF axis may be involved in the suppression of lung cancer cellular proliferation and development, and miR-144-3p may function as a potential therapeutic target in lung cancer treatment in the future.
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页数:12
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