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MiR-122-5p suppresses the proliferation, migration, and invasion of gastric cancer cells by targeting LYN
Author(s) -
Lei Meng,
Zhangming Chen,
Zhe Jiang,
Ting Huang,
Jie Hu,
Pan-Quan Luo,
Hongli Zhang,
Mengqi Huang,
Lei Huang,
Yu Chen,
Ming Lü,
Aman Xu,
Songcheng Ying
Publication year - 2019
Publication title -
acta biochimica et biophysica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/gmz141
Subject(s) - lyn , gene silencing , cancer research , western blot , microrna , cell growth , downregulation and upregulation , cell migration , biology , chemistry , proto oncogene tyrosine protein kinase src , cell culture , microbiology and biotechnology , signal transduction , gene , genetics
Gastric cancer (GC) is one of malignant tumors with high mortality and morbidity in the world. MicroRNA-122 (miR-122) acts as a tumor suppressor in a variety of cancers and has been found to be dominant in gastric adenocarcinoma. However, the specific biological function of miR-122-5p in GC is not completely clear. In this study, we found that miR-122-5p was low-expressed in GC tissues and cell lines by using qRT-PCR. Overexpression of miR-122-5p inhibited the proliferation, migration, and invasion of GC cells by using CCK-8 and transwell assays. On the contrary, downregulation of miR-122-5p promoted the proliferation, migration, and invasion of GC cells. In addition, we found that the expression of LYN, an Src family tyrosine kinase, was inversely correlated with miR-122-5p expression in GC tissues by using western blot analysis, immunohistochemistry, and qRT-PCR assays. Meanwhile, luciferase assay results indicated that LYN is a direct target of miR-122-5p in GC cells. Moreover, silencing LYN expression by its siRNA inhibited the proliferation, migration, and invasion of GC cells. Importantly, overexpression of LYN restored miR-122-5p-mediated inhibition of the proliferation, migration, and invasion of GC cells. Taken together, our results indicated miR-122-5p inhibited the proliferation, migration, and invasion by targeting LYN in GC.

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