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Minimal Invasive Resection of Large Retrosternal Thyroid Goiter
Published on: September 20, 2024
miR‑205 targets YAP1 and inhibits proliferation and invasion in thyroid cancer cells
Dewei Li1, Qiang Wang2, Ning Li3
1Department of Thyroid Surgery, Shanxi Provincial People's Hospital, Taiyuan, Shanxi 030012, P.R. China.
Abstract:
MicroRNA‑205 (miR‑205) has been reported to be downregulated, and serves critical roles in the pathogenesis and progression of several types of cancer, including breast, prostate and lung cancer. However, the underlying mechanism of miR‑205 in thyroid cancer remains unclear. In the present study, it was demonstrated that the expression of miR‑205 was reduced in thyroid cancer tissues compared with non‑cancer tissues. In addition, miR‑205‑knockdown models in the BHT‑101 cell line and ectopic expression models in the 8505‑C cell line were used to measure the biological functions of miR‑205. The results indicated that miR‑205 inhibited certain aspects of thyroid cancer, including cell proliferation, migration and invasion. Furthermore, Yes‑associated protein 1 (YAP1) was identified as a target gene of miR‑205 and its expression was negatively correlated with that of miR‑205 in thyroid cancer tissues. Depletion of YAP1 partially reduced the anti‑miR‑205‑induced cell growth and invasion. The results of the present study suggested that the tumor suppressive functions of miR‑205 via targeting YAP1 could be a novel target for the treatment of thyroid cancer.
Insights
MicroRNA-205 (miR-205) is reduced in thyroid cancer, inhibiting cell proliferation, migration, and invasion. Targeting Yes-associated protein 1 (YAP1) by miR-205 offers a potential new treatment strategy for thyroid cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-205 (miR-205) is implicated in various cancers but its role in thyroid cancer is not well understood.
- Previous studies show miR-205 downregulation in breast, prostate, and lung cancers, suggesting a tumor-suppressive function.
Purpose of the Study:
- To investigate the expression and functional role of miR-205 in thyroid cancer.
- To identify the molecular mechanism underlying miR-205's function in thyroid cancer, including its potential targets.
Main Methods:
- Quantitative analysis of miR-205 expression in thyroid cancer tissues versus non-cancerous tissues.
- Establishment of miR-205 knockdown (BHT-101) and overexpression (8505-C) cell models.
- Assessment of cell proliferation, migration, and invasion assays.
- Identification and validation of miR-205 target genes using molecular techniques.
Main Results:
- miR-205 expression was significantly reduced in thyroid cancer tissues compared to normal tissues.
- Reduced miR-205 levels were associated with increased thyroid cancer cell proliferation, migration, and invasion.
- Yes-associated protein 1 (YAP1) was identified as a direct target of miR-205, with inverse correlation in tumor tissues.
- YAP1 depletion partially reversed the effects of miR-205 inhibition on cell growth and invasion.
Conclusions:
- miR-205 acts as a tumor suppressor in thyroid cancer by targeting YAP1.
- The miR-205/YAP1 axis represents a potential therapeutic target for thyroid cancer treatment.
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