Effect and Molecular Mechanism of MiR-181a-5p on the Proliferation and Invasion of Papillary Thyroid Cancer Cells

Authors

  • Junwen Hao Department of Breast and Thyroid Surgery, Panyu Central Hospital Affiliated to Guangzhou Medical University, 511400 Guangzhou, Guangdong, China Author
  • Weijun Huang Department of Breast and Thyroid Surgery, Panyu Central Hospital Affiliated to Guangzhou Medical University, 511400 Guangzhou, Guangdong, China Author
  • Songming Li Department of Breast and Thyroid Surgery, Panyu Central Hospital Affiliated to Guangzhou Medical University, 511400 Guangzhou, Guangdong, China Author

Keywords:

Papillary thyroid cancer, MiR-181a-5p, Thyrotropin receptor, proliferation, invasion

Abstract

Objective: To investigate the effect and regulation mechanism of miR-181a-5p on papillary thyroid carcinoma (PTC) cells. Methods: The expressions of miR-181a-5p and thyrotropin receptor (TSHR) in PTC tissues, and the targeting relationship between these two genes were analyzed using bioinformatics tools, and their targeting relationship was verified by dual-luciferase reporter assay. After TPC-1 cells were transfected with miR-181a-5p inhibitor and shTSHR, the expression levels of miR-181a-5p, TSHR, E-cadherin, N-cadherin and Vimentin were detected by quantitative reverse transcription polymerase chain reaction or Western blot assay. The effects of miR-181a-5p and TSHR on the viability and invasion of TPC-1 cells were detected by MTT and Transwell assay. Results: The expression of miR-181a-5p was upregulated in PTC tissues and cells (p < 0.001), and the expression of TSHR was lowered in PC tissues. MiR-181a-5p could directly target TSHR. Downregulation of miR-181a-5p inhibited viability and invasion, and the expressions of N-cadherin and Vimentin (p < 0.01), but promoted the expression of E-cadherin in TPC-1 cells (p < 0.001). TSHR knockdown produced the opposite results (p < 0.01), and partially reversed the effect of miR-181a-5p downregulation on TPC-1 cells (p < 0.01). Conversely, down-regulation of miR-181a-5p could offset the effect of TSHR knockdown (p < 0.05). Conclusion: Downregulation of miR-181a-5p suppressed the malignant progression of PTC cells by promoting TSHR expression.

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Published

2025-05-30

Data Availability Statement

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding authors.

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Original Research