4.7 Article

SP1-induced lncRNA ZFPM2 antisense RNA 1 (ZFPM2-AS1) aggravates glioma progression via the miR-515-5p/Superoxide dismutase 2 (SOD2) axis

Journal

BIOENGINEERED
Volume 12, Issue 1, Pages 2299-2310

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21655979.2021.1934241

Keywords

ZFPM2-AS1; SP1; miR-515-5p; SOD2; glioma

Funding

  1. Nanjing Health Science and Technology Development Special Fund Project [YKK19166, YKK19167]

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ZFPM2-AS1 is a highly-expressed lncRNA in glioma tissues and cells, and its silencing suppresses cell proliferation, cell cycle, and promotes cell apoptosis. SP1 interacts with the ZFPM2-AS1 promoter to transcriptionally activate ZFPM2-AS1 expression, and ZFPM2-AS1 functions as a ceRNA for miR-515-5p to target SOD2 in glioma cells. This study highlights the regulatory mechanism of the SP1/ZFPM2-AS1/miR-515-5p/SOD2 axis in glioma and suggests that targeting ZFPM2-AS1 could be an effective treatment strategy for glioma.
Glioma is a common life-threatening tumor with high malignancy and high invasiveness. LncRNA ZFPM2 antisense RNA 1 (ZFPM2-AS1) was confirmed to be implicated in numerous tumors, while its biological function and mechanism have not been thoroughly understood in glioma. The gene expression was measured by RT-qPCR. Cell proliferation, cell cycle, and cell apoptosis of glioma cells were validated by CCK-8, colony formation, flow cytometry and TUNEL assays. The effect of ZFPM2-AS1 on tumor growth was verified by in vivo assay. The exploration on ZFPM2-AS1-mediated mechanism was carried out via ChIP, luciferase reporter, and RIP assays. In the present study, ZFPM2-AS1 was demonstrated as a highly-expressed lncRNA in glioma tissues and cells. ZFPM2-AS1 silencing suppressed cell proliferation and cell cycle, but facilitated cell apoptosis. In addition, the inhibitive effect of silenced ZFPM2-AS1 was also observed in tumor growth. Furthermore, we found that SP1 interacted with ZFPM2-AS1 promoter to transcriptionally activate ZFPM2-AS1 expression. Moreover, ZFPM2-AS1 was identified as a competing endogenous RNA (ceRNA) for miR-515-5p to target SOD2. Rescue assays verified that SOD2 overexpression partially abolished the suppressive impact of ZFPM2-AS1 silencing on glioma cell growth. In conclusion, this study corroborated the regulatory mechanism of SP1/ZFPM2-AS1/miR-515-5p/SOD2 axis in glioma, indicating that targeting ZFPM2-AS1 might be an effective way to treat glioma.

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