circSMAD2 inhibits the epithelial-mesenchymal transition by targeting miR-629 in hepatocellular carcinoma

Xianwei Zhang1, Ping Luo1, Wei Jing1

  • 1Department of Clinical Laboratory Medicine, Center for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.

Abstract

Insights

Circular RNA SMAD2 (circSMAD2) is downregulated in liver cancer and inhibits tumor cell migration and invasion. It achieves this by targeting microRNA-629 (miR-629), suppressing its expression and thus hindering cancer progression.

Area of Science:

  • Molecular Biology
  • Oncology
  • Non-coding RNA Research

Background:

  • Circular RNAs (circRNAs) are non-coding RNA molecules with emerging roles in biological processes.
  • Recent research highlights the involvement of circRNAs in the progression of various cancers, including hepatocellular carcinoma (HCC).

Purpose of the Study:

  • To investigate the expression and function of circRNA SMAD2 (circSMAD2) in hepatocellular carcinoma (HCC).
  • To elucidate the underlying molecular mechanism of circSMAD2 in regulating HCC progression, specifically its interaction with microRNA-629 (miR-629).

Main Methods:

  • Quantitative real-time polymerase chain reaction (qRT-PCR) to measure circSMAD2 expression in HCC and adjacent non-tumor tissues.
  • In vitro assays (proliferation, apoptosis, migration, invasion, Western blot) to assess circSMAD2's biological function.
  • Dual-luciferase reporter assay and co-transfection experiments to validate the interaction between circSMAD2 and miR-629 and their roles in HCC.

Main Results:

  • circSMAD2 expression was significantly downregulated in HCC tissues and associated with HCC differentiation.
  • Overexpression of circSMAD2 inhibited HCC cell migration, invasion, and epithelial-mesenchymal transition (EMT).
  • circSMAD2 directly targets and suppresses miR-629 expression in HCC cells, and this interaction is crucial for circSMAD2's tumor-suppressive effects.

Conclusions:

  • circSMAD2 acts as a tumor suppressor in HCC by inhibiting cell migration, invasion, and EMT.
  • The mechanism involves the direct targeting of miR-629 by circSMAD2, leading to the suppression of miR-629 activity.

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