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Updated: Apr 27, 2026

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
BTG1 expression in thyroid carcinoma: diagnostic indicator and prognostic marker
1Department of Endocrinology, Tangshan Workers Hospital, Tangshan 063000, P.R. China.
B cell translocation gene 1 (BTG1) is significantly lower in thyroid cancer, correlating with advanced disease and poor survival. Overexpressing BTG1 in thyroid cancer cells reduced proliferation, increased apoptosis, and inhibited migration, indicating BTG1 acts as a tumor suppressor.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Thyroid carcinoma is a significant global health concern.
- Understanding the molecular mechanisms underlying thyroid cancer progression is crucial for developing effective therapeutic strategies.
- B cell translocation gene 1 (BTG1) is a potential tumor suppressor gene, but its role in thyroid carcinoma remains unclear.
Purpose of the Study:
- To investigate the expression and functional role of BTG1 in thyroid carcinoma.
- To determine the correlation between BTG1 expression levels and clinicopathological features and prognosis of thyroid cancer patients.
- To elucidate the in vitro effects of BTG1 overexpression on thyroid cancer cell behavior.
Main Methods:
- Immunohistochemistry and western blotting were used to assess BTG1 expression in thyroid cancer tissues and adjacent normal tissues.
- A human thyroid cancer cell line (FTC-133) was stably transfected with a lentivirus to overexpress BTG1 (LeBTG1 cells).
- In vitro assays including MTT, flow cytometry, and Matrigel invasion assays were performed to evaluate cell viability, proliferation, apoptosis, cell cycle distribution, migration, and invasion.
Main Results:
- BTG1 protein expression was significantly lower in thyroid cancer tissues compared to normal tissues (36.1% vs. 80.0% for IHC, P<0.05).
- Reduced BTG1 expression correlated with lymph node metastasis, advanced clinical stage, poor pathological differentiation, and decreased 10-year survival rates (30.2% vs. 66.7%, P<0.05).
- In vitro, BTG1 overexpression in FTC-133 cells led to reduced cell survival, increased apoptosis, G0/G1 cell cycle arrest, and impaired migration and invasion, accompanied by decreased expression of cyclin D1, Bcl-2, and MMP-9.
Conclusions:
- BTG1 expression is significantly downregulated in thyroid carcinoma.
- BTG1 acts as a negative regulator of thyroid cancer progression by inhibiting cell proliferation, survival, and metastasis.
- BTG1 serves as a potential prognostic biomarker for thyroid cancer.
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