LINC01291 promotes hepatocellular carcinoma development by targeting miR‐186‐5p/OXSR1 axis

Background

Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide. Recent studies have demonstrated that lncRNAs play an important role in tumorigenesis. LINC01291 has been proven to be involved in the proliferation and migration of different cancers, but the function of LINC01291 in HCC is still unknown.

Methods

First, the expression of LINC01291 in 50 paired HCC tissues, adjacent normal tissues and HCC cell lines was measured by qRT-PCR. Then, the function of LINC01291 in HCC cell proliferation, migration and invasion was measured by colony formation, Cell Counting Kit-8 (CCK8) assays, wound healing assays and Transwell assays. In addition, E-cadherin, N-cadherin, vimentin and OXSR1 protein expression levels were assessed via western blotting. Luciferase reporter assays were used to prove the relationship between LINC01291 and miR-186-5p as well as miR-186-5p and OXSR1 mRNA. Rescue assays and in vivo experiments further confirmed the LINC01291/miR-186-5p/OXSR1 axis in the progression of HCC.

Results

LINC01291 was upregulated in both HCC tissues and cell lines. Knockdown of LINC01291 inhibited the proliferation, migration, invasion and EMT progression of HCC cells. In addition, LINC01291 could overexpress OXSR1 by sponging miR-186-5p, and OXSR1 overexpression or miR-186-5p inhibition could rescue the effect of LINC01291 knockdown in YY-8103 cell lines. In addition, lentiviral sh-LINC01291 could effectively inhibit the growth of subcutaneous YY-8103 xenograft tumors, while the anticancer effect could be reversed by cotransfection with in-miR-186-5p or ov-OXSR1.

Conclusions

LINC01291 can promote the proliferation, migration, invasion and EMT of HCC cells via the miR-186-5p/OXSR1 axis, and sh-LINC01291 can inhibit tumor growth in a xenograft mouse model.

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