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CircSKA3 通过胶质母细胞瘤中的甲基化下调 miR-1,以促进癌细胞增殖
Authors Zhou M, Li H, Chen K, Ding W, Yang C, Wang X
Received 27 August 2020
Accepted for publication 7 November 2020
Published 19 January 2021 Volume 2021:13 Pages 509—514
DOI https://doi.org/10.2147/CMAR.S279097
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Seema Singh
Background: Circular RNA circSKA3 plays an oncogenic role in breast cancer, while its role in glioblastoma (GBM) is unknown. This study aimed to explore the role of circSKA3 in GBM.
Methods: Differential expression of circSKA3 and miR-1 in GBM and adjacent non-cancer tissue samples were analyzed by RT-qPCR. GBM cells were transfected with circSKA3 expression vector or miR-1 mimic, followed by RT-qPCR to explore the potential crosstalk between them. Methylation-specific PCR (MSP) was carried out to assess the role of circSKA3 in regulating the methylation of miR-1 gene. The role of circSKA3 and miR-1 in regulating GBM cell proliferation was analyzed by CCK-8 assay.
Results: We found that circSKA3 was upregulated in GBM and inversely correlated with miR-1 across GBM tissues. High expression levels of circSKA3 and low expression levels of miR-1 were significantly correlated with the poor survival of GBM patients. In GBM cells, overexpression of circSKA3 increased the methylation of miR-1 gene and decreased the expression of miR-1. CCK-8 assay showed that overexpression of circSKA3 reduced the inhibitory effects of miR-1 on cell proliferation.
Conclusion: Therefore, circSKA3 may downregulate miR-1 through methylation in GBM to promote cancer cell proliferation.
Keywords: glioblastoma, circSKA3, miR-1, methylation