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Updated: Oct 26, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1
Yuxia Wang1, Zhaozhe Liu2, Xiangning Ren1
1Department of Endocrinology, The Fourth Affiliated Hospital of China Medical University, Shenyang 110032, Liaoning, China.
Background:
Thyroid carcinoma (TC) is one of the frequent endocrine malignancies, and growing evidence suggests that aberrant microRNA (miRNA) expression contributes to TC development and progression. Nevertheless, the function of miR-330-5p in the progression of TC remains unknown.
Methods:
The expression levels of miR-330-5 in patients with thyroid carcinoma and healthy controls were detected, and their potential diagnostic and prognostic values were analyzed.
Results:
In this study, we firstly found that miR-330-5p expression was markedly upregulated in TC tissue and cell lines. Functionally, the downregulation of miR-330-5p suppressed TC cell proliferation, migration, and invasion. Further studies revealed that miR-330-5p negatively regulated the expression of forkhead box E1 (FOXE1). More importantly, the results of rescue experiments suggested that FOXE1 overexpression reduced the positive effects of miR-330-5p overexpression in TPC-1 and K-1 cells.
Conclusions:
This work revealed that miR-330-5p facilitated the TC progression through targeting FOXE1, which may offer novel therapeutic options for TC.
Insights
MicroRNA miR-330-5p is upregulated in thyroid carcinoma (TC), promoting cancer progression by targeting FOXE1. Inhibiting miR-330-5p may offer new therapeutic strategies for TC patients.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Thyroid carcinoma (TC) is a common endocrine malignancy.
- Aberrant microRNA (miRNA) expression is implicated in TC development and progression.
- The specific role of miR-330-5p in TC progression was previously unknown.
Purpose of the Study:
- To investigate the expression and function of miR-330-5p in thyroid carcinoma.
- To determine the diagnostic and prognostic value of miR-330-5p in TC.
- To elucidate the molecular mechanism underlying miR-330-5p's role in TC progression.
Main Methods:
- Analysis of miR-330-5p expression levels in TC tissues and cell lines compared to controls.
- Functional assays to assess the impact of miR-330-5p downregulation on TC cell proliferation, migration, and invasion.
- Investigation of miR-330-5p's interaction with forkhead box E1 (FOXE1) and rescue experiments.
Main Results:
- miR-330-5p was significantly upregulated in TC tissues and cell lines.
- Downregulation of miR-330-5p inhibited TC cell proliferation, migration, and invasion.
- miR-330-5p was found to negatively regulate FOXE1 expression, and FOXE1 overexpression counteracted miR-330-5p's pro-tumor effects.
Conclusions:
- miR-330-5p promotes thyroid carcinoma progression by targeting FOXE1.
- This finding suggests that miR-330-5p could be a potential therapeutic target for TC.
- Targeting the miR-330-5p/FOXE1 axis may offer novel treatment strategies for thyroid carcinoma.
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