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LncRNA MCM3AP-AS1 通过海绵化 miR-545上 调 CDK4,从而抑制结直肠癌 G1 期阻滞
Authors Ma X, Luo J, Zhang Y, Sun D, Lin Y
Received 26 January 2020
Accepted for publication 30 July 2020
Published 7 September 2020 Volume 2020:12 Pages 8117—8124
DOI https://doi.org/10.2147/CMAR.S247330
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Antonella D'Anneo
Introduction: This study aimed to investigate the role of lncRNA MCM3AP-AS1 in colorectal cancer (CRC).
Methods: Paired tumor and non-tumor tissues were collected from 60 CRC patients. Expression of MCM3AP-AS1 was determined by RT-qPCR. Overexpression of MCM3AP-AS1, miR-545, and CDK4 in CRC cells was achieved to explore the interactions between them. Cell cycle assay was performed to analyze the roles of MCM3AP-AS1, miR-545, and CDK4 in regulating the cell cycle progression of CRC cells.
Results: We found that MCM3AP-AS1 was upregulated in CRC and its high expression levels predicted poor survival of CRC patients. MCM3AP-AS1 is predicted to interact with miR-545. In CRC cells, overexpression of MCM3AP-AS1 and miR-545 was achieved, while their overexpression did not affect the expression of each other. Instead, overexpression of MCM3AP-AS1 led to the increased expression levels of CDK4, which is a downstream target of miR-545. Cell cycle analysis showed that overexpression of MCM3AP-AS1 and CDK4 suppressed G1 arrest induced by miR-545. In addition, overexpression of MCM3AP-AS1 reduced the enhancing effects of overexpressing miR-545 on cell cycle progression.
Conclusion: MCM3AP-AS1 may upregulate CDK4 by sponging miR-545 to induce G1 arrest in CRC cells.
Keywords: MCM3AP-AS1, colorectal cancer, miR-545, CDK4, G1 arrest
