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Updated: Feb 13, 2026

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
miR-132 Targets FOXA1 and Exerts Tumor-Suppressing Functions in Thyroid Cancer
Xin Chen1, Mingzhe Li2, Hongwei Zhou1
1Department of Radiology, the First Hospital of Jilin University, Changchun, Jilin, P.R. China.
Abstract:
MicroRNA-132 (miR-132) has been demonstrated to be a tumor suppressor in several types of tumors. However, the expression and the role of miR-132 in human thyroid cancer are still poorly understood. The aim of the present study was to examine the potential roles and molecular mechanism of miR-132 in thyroid cancer. We found that miR-132 expression levels were significantly downregulated in thyroid cancer tissues and cell lines. Function assays showed that overexpression of miR-132 in TPC1 cells inhibited cell proliferation, migration, and invasion. Forkhead box protein A1 (FOXA1) was identified as a direct target of miR-132 in thyroid cancer cells. Knockdown of FOXA1 in TPC1 cells significantly inhibited cell proliferation, migration, and invasion, which mimicked the suppressive effect induced by miR-132 overexpression. Restoration of FOXA1 expression partially reversed the suppressive effect induced by miR-132 overexpression. Taken together, these results suggested that miR-132 acts as a tumor suppressor in thyroid cancer through targeting FOXA1.
Insights
MicroRNA-132 (miR-132) functions as a tumor suppressor in thyroid cancer. Its downregulation inhibits cell proliferation, migration, and invasion by targeting Forkhead box protein A1 (FOXA1).
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-132 (miR-132) is a known tumor suppressor in various cancers.
- The specific role and expression of miR-132 in human thyroid cancer remain largely uncharacterized.
Purpose of the Study:
- To investigate the expression levels and functional significance of miR-132 in human thyroid cancer.
- To elucidate the molecular mechanism underlying miR-132's action in thyroid cancer.
Main Methods:
- Quantitative real-time PCR to assess miR-132 expression in thyroid cancer tissues and cell lines.
- In vitro functional assays (proliferation, migration, invasion) following miR-132 overexpression in TPC1 cells.
- Western blotting and luciferase reporter assays to identify and validate Forkhead box protein A1 (FOXA1) as a direct miR-132 target.
- Gene knockdown and restoration experiments to confirm the role of FOXA1 in miR-132-mediated effects.
Main Results:
- miR-132 expression was significantly downregulated in thyroid cancer tissues and cell lines compared to normal controls.
- Overexpression of miR-132 suppressed proliferation, migration, and invasion of TPC1 thyroid cancer cells.
- Forkhead box protein A1 (FOXA1) was identified as a direct downstream target of miR-132.
- Knockdown of FOXA1 mimicked the inhibitory effects of miR-132, while FOXA1 restoration partially reversed these effects.
Conclusions:
- miR-132 acts as a tumor suppressor in human thyroid cancer.
- The tumor-suppressive function of miR-132 is mediated, at least in part, by its direct targeting of FOXA1.
- These findings highlight miR-132 as a potential therapeutic target for thyroid cancer.
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