4.4 Article

Circ_0003356 suppresses gastric cancer growth through targeting the miR-668-3p/SOCS3 axis

Journal

WORLD JOURNAL OF GASTROINTESTINAL ONCOLOGY
Volume 15, Issue 5, Pages 787-809

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.4251/wjgo.v15.i5.787

Keywords

Epithelial-mesenchymal transition; Circ_0003356; Gastric cancer; Invasion; Proliferation; Migration

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The downregulation of circ_0003356 and the upregulation of miR-668-3p were observed in gastric cancer cells. Overexpression of circ_0003356 inhibited the migration, proliferation, and invasion of gastric cancer cells and promoted apoptosis. Through its interaction with miR-668-3p, circ_0003356 regulated the biological behaviors of gastric cancer cells, with SOCS3 as a downstream target of miR-668-3p.
BACKGROUND Circular RNAs (circRNAs) have attracted extensive attention as therapeutic targets in gastric cancer (GC). Circ_0003356 is known to be downregulated in GC tissues, but its cellular function and mechanisms remain undefined. AIM To investigate the role of circ_0003356 in GC at the molecular and cellular level. METHODS Circ_0003356, miR-668-3p, and SOCS3 expression were assessed via quantitative real time-polymerase chain reaction (qRT-PCR). Wound healing, EdU, CCK-8, flow cytometry and transwell assays were used to analyze the migration, proliferation, viability, apoptosis and invasion of GC cells. The subcellular localization of circ_0003356 was monitored using fluorescence in situ hybridization. The interaction of circ_0003356 with miR-668-3p was confirmed using RIP-qRT-PCR, RNA pull-down, and dual luciferase reporter assays. We observed protein levels of genes via western blot. We injected AGS cells into the upper back of mice and performed immunohistochemistry staining for examining E-cadherin, N-cadherin, Ki67, and SOCS3 expressions. TUNEL staining was performed for the assessment of apoptosis in mouse tumor tissues. RESULTS Circ_0003356 and SOCS3 expression was downregulated in GC cells, whilst miR-668-3p was upregulated. Exogenous circ_0003356 expression and miR-668-3p silencing suppressed the migration, viability, proliferation, epithelial to mesenchymal transition (EMT) and invasion of GC cells and enhanced apoptosis. Circ_0003356 overexpression impaired tumor growth in xenograft mice. Targeting of miR-668-3p by circ_0003356 was confirmed through binding assays and SOCS3 was identified as a downstream target of miR-668-3p. The impacts of circ_0003356 on cell proliferation, apoptosis, migration, invasion and EMT were reversed by miR-668-3p up-regulation or SOCS3 downregulation in GC cells. CONCLUSION Circ_0003356 impaired GC development through its interaction with the miR-668-3p/SOCS3 axis.

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