MicroRNA-139 targets fibronectin 1 to inhibit papillary thyroid carcinoma progression

Ying Ye1, Juhua Zhuang1, Guoyu Wang1

  • 1Department of Nuclear Medicine, The Seventh People's Hospital of Shanghai University of Traditional Chinese Medicine, Shanghai 200137, P.R. China.

Oncology Letters
|December 19, 2017
PubMed

Insights

MicroRNA-139 (miR-139) is downregulated in papillary thyroid carcinoma (PTC), suppressing tumor growth and invasion. Targeting fibronectin 1 (FN1) by miR-139 inhibits tumorigenesis, suggesting its potential as a therapeutic target for PTC.

Area of Science:

  • Endocrinology
  • Molecular Biology
  • Oncology

Background:

  • Thyroid cancer, particularly papillary thyroid carcinoma (PTC), shows increasing incidence.
  • MicroRNAs (miRNAs) are implicated in PTC development and progression.
  • The role of miR-139 in PTC remains unclear.

Purpose of the Study:

  • To investigate the expression, function, and molecular mechanism of miR-139 in PTC.
  • To identify potential molecular targets of miR-139 in PTC.
  • To evaluate miR-139 as a potential biomarker and therapeutic target for PTC.

Main Methods:

  • Quantitative real-time PCR to assess miR-139 expression in PTC tissues and cell lines.
  • In vitro assays to evaluate the effects of miR-139 restoration on PTC cell proliferation and invasion.
  • Western blotting and luciferase reporter assays to identify and validate miR-139 targets.

Main Results:

  • miR-139 expression was significantly downregulated in PTC tissues and cell lines.
  • Restoration of miR-139 suppressed PTC cell proliferation and invasion in vitro.
  • Fibronectin 1 (FN1) was identified as a direct target of miR-139, and its expression was inversely correlated with miR-139 levels in PTC.
  • Overexpression of FN1 partially reversed the tumor-suppressive effects of miR-139.

Conclusions:

  • miR-139 acts as a tumor suppressor in PTC by targeting FN1.
  • miR-139 plays a critical role in inhibiting PTC tumorigenesis.
  • miR-139 holds potential as a diagnostic biomarker and therapeutic target for PTC.