Silencing of Long Noncoding RNA LINC00324 Interacts with MicroRNA-3200-5p to Attenuate the Tumorigenesis of Gastric Cancer via Regulating BCAT1

Abstract EN

Purpose.

This study was aimed at exploring the effect of long noncoding RNA LINC00324 (LINC00324) on gastric cancer (GC) and the potential molecular mechanisms.

Methods.

The expression of LINC00324 and miR-3200-5p in GC tissues and cells was detected by qRT-PCR.

LINC00324 was silenced in GC cells by transfection of si-LINC00324.

Then, the proliferation, migration, and invasion of GC cells were analyzed by MTT, wound healing, and transwell assays, respectively.

The interactions between LINC00324 and miR-3200-5p and between miR-3200-5p and BCAT1 were determined by a dual-luciferase reporter and/or RNA pull-down assay.

Results.

The expression of LINC00324 was upregulated in GC cells and tissues, but miR-3200-5p was downregulated.

Silencing of LINC00324 inhibited the proliferation, migration, and invasion of GC cells.

LINC00324 directly targeted miR-3200-5p, and miR-3200-5p directly targeted BCAT1.

si-LINC00324 negatively regulated BCAT1 expression via binding to miR-3200-5p.

Furthermore, silencing of LINC00324 reversed the promoting effects of BCAT1 on the proliferation, migration, and invasion of GC cells.

Conclusion.

Silencing of LINC00324 inhibited the proliferation, migration, and invasion of GC cells through regulating the miR-3200-5p/BCAT1 axis.