Vitamin D3 mediates miR-15a-5p inhibition of liver cancer cell proliferation via targeting E2F3.

Oncol Lett

Department of Gastroenterology, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, P.R. China.

Published: July 2020

AI Article Synopsis

  • Vitamin D3 has been shown to inhibit liver cancer growth and progression, though its exact mechanism remains unclear.
  • The study explored the effects of vitamin D3 and miR-15a-5p on liver cancer cells using various assays, revealing that vitamin D3 promotes miR-15a-5p expressions, leading to increased cancer cell death.
  • E2F transcription factor 3 (E2F3) was identified as a target of miR-15a-5p; silencing E2F3 also suppressed liver cancer cell proliferation, indicating potential therapeutic pathways for liver cancer treatment.

Article Abstract

Vitamin D3 has been demonstrated to suppress the development and progression of liver cancer, but the mechanism is unclear. The effects of vitamin D3 and microRNA (miR)-15a-5p on liver cancer cells were investigated in the present study using MTT and colony formation assays, flow cytometry, western blotting and reverse transcription-quantitative PCR. A dual-luciferase reporter assay was performed to determine whether E2F transcription factor 3 (E2F3) was a target of miR-15a-5p. The effects of silencing the E2F3 gene expression in liver cancer cells were investigated using a small interfering RNA. Vitamin D3 suppressed liver cancer cell proliferation, induced apoptosis and increased miR-15a-5p expression. Treatment with the miR-15a-5p mimics significantly suppressed liver cancer cell proliferation compared with that of the controls. Bioinformatics analysis and a dual-luciferase reporter assay demonstrated that E2F3 was a target of miR-15a-5p and that silencing E2F3 inhibited liver cancer cell proliferation. Therefore, Vitamin D3 suppressed cell proliferation by miR-15a-5p-mediated silencing of E2F3 gene expression. These findings suggested a role for vitamin D3 and E2F3 targeting as potential novel liver cancer therapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285896PMC
http://dx.doi.org/10.3892/ol.2020.11572DOI Listing

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