LncRNA DCST1-AS1 downregulates miR-29b through methylation in glioblastoma (GBM) to promote cancer cell proliferation

下调和上调 细胞生长 甲基化 癌症研究 细胞 医学 DNA甲基化 癌症 生物 基因表达 内科学 基因 遗传学 生物化学
作者
Siqin Hu,Yiqun Yao,Xiao Hu,Yanfeng Zhu
出处
期刊:Clinical & Translational Oncology [Springer Science+Business Media]
卷期号:22 (12): 2230-2235 被引量:13
标识
DOI:10.1007/s12094-020-02363-1
摘要

The role of DCST1-AS1 has been investigated in several types of cancer, while the role of DCST1-AS1 in glioblastoma (GBM) is unclear. This study aimed to investigate the role of DCST1-AS1 in GBM. GBM and paired non-tumor tissues were collected from 62 GBM patients. Expression levels of DCST1-AS1 and miR-29b in paired tissue samples were determined by RT-qPCR. The role of DCST1-AS1 in regulating the methylation of miR-29b was assessed by methylation-specific PCR (MSP). Cell proliferation was analyzed by cell proliferation assay. It was observed that the upregulation of DCST1-AS1 in GBM predicted poor survival. MiR-29b was downregulated in GBM and inversely correlated with the expression of DCST1-AS1. In GBM cells, overexpression of DCST1-AS1 resulted in the downregulation of miR-29b and the increased methylation level of miR-29b gene. Overexpression of DCST1-AS1 resulted in increased cell proliferation. Moreover, Overexpression of DCST1-AS1 significantly reversed the inhibitory effects of miR-29b on cancer cell proliferation. DCST1-AS1 may downregulate miR-29b through methylation in GBM to promote cancer cell proliferation.

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