Can small nucleolar RNA be a novel molecular target for hepatocellular carcinoma?

Han Shuwen1, Yang Xi2, Qi Quan3

  • 1Department of Oncology, Huzhou Cent Hosp, Affiliated Cent Hops HuZhou University, 198 Hongqi Rd, Huzhou, Zhejiang, PR China.

Gene
|January 25, 2020
PubMed
Abstract

Insights

Small nucleolar RNAs (snoRNAs) are linked to hepatocellular carcinoma (HCC). These molecules, including small nucleolar RNA host genes (SNHGs), can influence tumor development and represent potential therapeutic targets for HCC.

Area of Science:

  • Oncology
  • Molecular Biology
  • RNA Biology

Background:

  • Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality worldwide.
  • Emerging research indicates a significant association between small nucleolar RNAs (snoRNAs) and HCC development.

Purpose of the Study:

  • To investigate the potential of snoRNAs as molecular targets for hepatocellular carcinoma.
  • To elucidate the role of specific snoRNAs and small nucleolar RNA host genes (SNHGs) in HCC pathogenesis.

Main Methods:

  • A systematic literature review was conducted using PubMed, Embase, and Cochrane databases up to August 12, 2019.
  • Included studies focused on the correlation between SNHGs and HCC (26 studies) and snoRNAs and HCC (8 studies).
  • A correlation network diagram was constructed to visualize the relationships between snoRNAs and HCC.

Main Results:

  • Specific SNHGs (e.g., SNHG1, SNHG6, SNHG16, SNHG20) exhibit diverse roles in HCC, promoting or inhibiting tumorigenesis.
  • SNORD76 promotes tumor cell proliferation, and its pathway overlaps with snoU2_19.
  • Several snoRNAs and SNHGs (SNHG3, SNHG20, SNHG6, SNORD76, snoRA47, SNHG16, snoU2_19) modulate epithelial-mesenchymal transition (EMT) and the Wnt/β-catenin signaling pathway in HCC.

Conclusions:

  • snoRNAs regulate HCC occurrence by modulating multiple molecular signaling pathways.
  • snoRNAs demonstrate potential as molecular targets for HCC therapy.

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