4.5 Article

Circular RNA circ_0051620 sponges miR-338-3p and regulates ADAM17 to promote the gastric cancer progression

Journal

PATHOLOGY RESEARCH AND PRACTICE
Volume 233, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.prp.2022.153887

Keywords

Gastric cancer; Circ_0051620; MiR-338-3p; ADAM17

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This study found that overexpression of circ_0051620 is associated with the progression and poor prognosis of GC, promoting development and metastasis by sponging miR-338-3p and decoying ADAM17.
Background: Gastric cancer (GC) is the fifth most common threatening cancer-related death globally. Recent studies indicate that circRNAs play a critical role in various biological and pathogenesis processes, including proliferation, apoptosis, and invasion of GC through sponging different miRNAs. However, the in-depth investigations of circRNAs in the progression of GC remains unclear, therefore in the current study, we aimed to investigate the mechanism behind the circular RNA circ_0051620 in the progression of GC through spooning the miR-338-3p and ADAM17. Methods: At first, circRNA microarray was used to identify the expression profiles of circRNA in GC tissues. Further, qRT-PCR was performed to detect genes expression. Then, the clinical significance of circ_0051620 was evaluated. Afterward, bioinformatical database, dual-luciferase reporter assays were used to determine the regulatory networks of circ_0051620 and miR-338-3p in GC cells respectively. The Transwell experiments were used to explore the effects of circ_0051620, miR-338-3p, ADAM17 on the migration and invasion of GC cells. Results: qRT-PCR results indicated that circ_0051620 in GC was over-expressed in tumoral tissues and cell lines compared to the normal controls. Moreover, miR-338-3p was confirmed to be the target of circ_0051620. Overall overexpression of miR-338-3p inhibited the cell migration, invasion through inhibiting ADAM17 in GC cells. Conclusion: The overexpression of circ_0051620 is found to be associated with progress and poor prognosis of GC, promoting the development and metastasis via sponging miR-338-3p and decoying ADAM17

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