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Updated: Feb 16, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
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.
Abstract:
Thyroid cancer is the most common tumour of the endocrine system, and its incidence rate has markedly increased over the past several decades. Aberrantly expressed microRNAs (miRNAs) are reportedly involved in the formation and progression of papillary thyroid carcinoma (PTC) by regulating their target genes. Thus, miRNAs may be potential molecular biomarkers for the prediction and prognosis of PTC, and also as novel therapeutic targets for patients with PTC. miR-139 has recently been reported to be aberrantly expressed in several types of cancer. However, the expression levels, biological functions and the associated molecular mechanism of miR-139 in PTC have not been clearly elucidated. The results of the present study revealed that miR-139 expression was downregulated in PTC tissues and cell lines when compared with adjacent normal tissues and normal human thyroid cells, respectively. The restoration of miR-139 expression suppressed cellular proliferation and invasion in PTC in vitro. In addition, fibronectin 1 (FN1) was identified as a direct target of miR-139 in PTC. Furthermore, FN1 was highly expressed in PTC tissues and negatively associated with miR-139 expression. Moreover, the tumour-suppressive effects of miR-139 overexpression on PTC cells were ameliorated by ectopic FN1 expression. To the best of our knowledge, the present study is the first to demonstrate that miR-139 may serve as a tumour suppressor and serve important roles in inhibiting tumourigenesis by targeting FN1 in PTC cells.
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.
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