Long noncoding RNA SNHG8 promotes the proliferation of osteosarcoma cells by downregulating miR-542-3p

G B Zhong1, C Q Jiang2, X S Yu2

  • 1Baoshan Branch, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University. Shanghai, China.

Insights

Long noncoding RNA SNHG8 promotes osteosarcoma progression by downregulating miR-542-3p. This lncRNA (SNHG8) is linked to poor survival and recurrence in osteosarcoma patients.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Small nucleolar RNA host genes (SNHGs) are long noncoding RNAs (lncRNAs) implicated in various cancers.
  • The specific role and molecular mechanisms of lncRNA SNHG8 in osteosarcoma (OS) pathogenesis are not well understood.

Purpose of the Study:

  • To investigate the role and molecular mechanisms of lncRNA SNHG8 in osteosarcoma.
  • To determine the correlation between SNHG8, miR-542-3p, and clinical outcomes in OS patients.

Main Methods:

  • TCGA cohort analysis for SNHG8 and miR-542-3p expression correlation with clinicopathological features and prognosis.
  • In vitro assays (MTT, Transwell) to assess cell viability and invasion.
  • Luciferase reporter assay to confirm the interaction between SNHG8 and miR-542-3p.
  • qRT-PCR to analyze SNHG8's effect on miR-542-3p expression in OS cell lines (MG-63, SW-1353).

Main Results:

  • Elevated SNHG8 expression or decreased miR-542-3p expression correlated with poor survival and tumor recurrence in OS patients.
  • Overexpression of SNHG8 enhanced proliferation and invasion in MG-63 cells, while silencing SNHG8 inhibited these processes in SW-1353 cells.
  • SNHG8 negatively regulated miR-542-3p expression and directly interacted with it, thereby attenuating SNHG8-induced cell proliferation.

Conclusions:

  • lncRNA SNHG8 promotes osteosarcoma cell proliferation and invasion.
  • SNHG8 exerts its oncogenic effects by downregulating miR-542-3p, suggesting a potential therapeutic target for osteosarcoma.

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