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Updated: Feb 13, 2026

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
Expression of serine peptidase inhibitor Kunitz type 1 in differentiated thyroid cancer
Chien-Liang Liu1,2, Po-Sheng Yang1, Ming-Nan Chien3
1Department of Surgery, MacKay Memorial Hospital and Mackay Medical College, 92, Section 2, Chung-Shan North Road, Taipei, 10449, Taiwan.
Abstract:
SPINT1, also known as HAI-1, is a Kunitz-type serine protease inhibitor that inhibits multiple proteases including hepatocyte growth factor (HGF) activator and matriptase. SPINT1 has been shown to modulate HGF/MET activation in certain cancer types. In the present study, we analyzed microarray datasets and found that SPINT1 was consistently upregulated in differentiated thyroid cancer. SPINT1 protein expression was investigated using tissue microarrays and independent samples of our 143 patients. Strong SPINT1 expression was observed in 61-68% of papillary thyroid cancer and 41-50% of follicular thyroid cancer. The overexpression diminished in anaplastic thyroid cancer. The SPINT1 expression in normal thyroid tissues and benign thyroid lesions was low. Furthermore, we noted that the SPINT1 expression was associated with extrathyroidal invasion, lymphovascular invasion, lymph node metastasis, advanced TNM stage, and a higher risk of recurrence in differentiated thyroid cancer. The results were in accordance with our analysis of The Cancer Genome Atlas data. In conclusion, an overexpression of SPINT1 appears to be associated with an invasive phenotype in differentiated thyroid cancer.
Insights
SPINT1 (serine protease inhibitor) is overexpressed in differentiated thyroid cancer, correlating with invasive features and recurrence risk. This suggests SPINT1 may drive thyroid cancer progression.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- SPINT1 (serine protease inhibitor) is a Kunitz-type inhibitor of proteases like HGF activator and matriptase.
- SPINT1 modulates HGF/MET signaling, implicated in cancer development.
- Upregulation of SPINT1 has been observed in various cancer types.
Purpose of the Study:
- To investigate SPINT1 expression patterns in differentiated thyroid cancer.
- To determine the correlation between SPINT1 expression and clinicopathological features of thyroid cancer.
- To assess the prognostic significance of SPINT1 in differentiated thyroid cancer.
Main Methods:
- Analysis of microarray datasets for SPINT1 gene expression.
- Quantitative assessment of SPINT1 protein expression using tissue microarrays in 143 patients.
- Correlation analysis between SPINT1 expression and clinicopathological parameters (invasion, metastasis, TNM stage, recurrence).
- Validation using The Cancer Genome Atlas (TCGA) data.
Main Results:
- SPINT1 was consistently upregulated in differentiated thyroid cancer (papillary and follicular) compared to normal thyroid tissues and benign lesions.
- Overexpression was less pronounced in anaplastic thyroid cancer.
- SPINT1 expression correlated significantly with extrathyroidal invasion, lymphovascular invasion, lymph node metastasis, advanced TNM stage, and increased recurrence risk.
- TCGA data analysis supported these findings.
Conclusions:
- SPINT1 is frequently overexpressed in differentiated thyroid cancer.
- SPINT1 overexpression is associated with aggressive clinicopathological features and a higher risk of recurrence.
- SPINT1 may play a role in promoting an invasive phenotype in differentiated thyroid cancer.
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