4.4 Article

CircRNA Hsa_circ_0001017 Inhibited Gastric Cancer Progression via Acting as a Sponge of miR-197

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DIGESTIVE DISEASES AND SCIENCES
卷 66, 期 7, 页码 2261-2271

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SPRINGER
DOI: 10.1007/s10620-020-06516-8

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Gastric cancer; Hsa_circ_0001017; Competing endogenous RNA; miR-197; Ras homolog family member B

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The study revealed that the upregulation of hsa_circ_0001017 significantly inhibited proliferation and metastasis of gastric cancer cell lines by targeting the miR-197/RHOB signaling pathway. The findings suggest that hsa_circ_0001017 could serve as a potential biomarker for gastric cancer treatment.
Background Gastric cancer (GC) is one of the most common digestive system diseases and yet lacks effective therapeutic regimen. Aims The aim of our present research was to probe the value of hsa_circ_0001017 in GC treatment. Methods qRT-PCR and Western blot were performed to detect gene and protein expressions, respectively. CCK-8 assay and clone formation assay were used to ensure the proliferation of GC cell lines. Transwell assay was performed to measure the migration and invasion of GC cell lines. The relationship between hsa_circ_0001017 and miR-197 and that between miR-197 and RHOB 3 '-UTR were ensured using the luciferase reporter assay. Results Decreased hsa_circ_0001017 was discovered in GC, and upregulation of hsa_circ_0001017 notably repressed proliferation, migration, and invasion of GC cell lines. We further certificated that hsa_circ_0001017 served as miR-197 sponge and suppressed the expression of miR-197. Moreover, hsa_circ_0001017 upregulation meaningfully accelerated RHOB expression in both gene and protein levels, and RHOB was a downstream target of miR-197. Overexpression of miR-197 could markedly restrain hsa_circ_0001017-induced RHOB increasing and stifle inhibition of hsa_circ_0001017 to the malignant phenotype of GC cell lines. Next, our results further confirmed that hsa_circ_0001017 increasing notably inhibited tumor growth, impeded miR-197 production, while it enhanced the expression of RHOB in vivo. Conclusion Our data demonstrated that upregulation of hsa_circ_0001017 could notably muffle the proliferation as well as the metastasis of GC cell lines and impede the formation of GC tumor via targeting to miR-197/RHOB signaling pathway. Our results evidenced that hsa_circ_0001017 may act as a rising biomarker for GC treatment.

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