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Updated: Jul 13, 2025

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
Agrin is a novel oncogenic protein in thyroid cancer
Anna Adamiok-Ostrowska1, Małgorzata Grzanka1, Barbara Czarnocka1
1Department of Biochemistry and Molecular Biology, Centre of Postgraduate Medical Education, 01-813 Warsaw, Poland.
Abstract:
Agrin (AGRN) is a matricellular glycoprotein involved in extracellular signal transduction. AGRN is involved in tumorigenesis and cancer progression; however, the role of AGRN in thyroid cancer (TC) remains unclear. In the present study, using cell lines derived from various subtypes of TC including CGTH, FTC-133 and BcPAP and transcriptomic data from patients with TC, the role of AGRN in TC was analyzed by migration, invasion, viability and proliferation assays as well as Western blot with EMT markers. AGRN expression was significantly increased in thyroid tumors and cell lines derived from various TC subtypes. The highest AGRN expression was found in follicular and papillary thyroid carcinoma subtypes. Immunocytochemistry revealed nuclear AGRN localization in normal (NTHY) and TC cells. Silencing of AGRN decreased viability, proliferation, migration and invasion of TC cell lines by upregulating vimentin and downregulating N-cadherin and E-cadherin. Furthermore, the expression of AGRN was associated with neutrophil infiltration in thyroid tumors. In conclusion, the present results indicated that increased AGRN expression promoted tumorigenic phenotypes of TC cells, while AGRN expression was associated with immune infiltration in thyroid tumors. AGRN may represent a target for future cancer therapy and requires further evaluation.
Insights
Increased agrin (AGRN) expression promotes thyroid cancer progression and immune infiltration. Silencing AGRN reduced cancer cell viability, migration, and invasion, suggesting AGRN as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Agrin (AGRN), a matricellular glycoprotein, is implicated in tumorigenesis and cancer progression.
- The specific role of AGRN in thyroid cancer (TC) pathogenesis is not well understood.
Purpose of the Study:
- To investigate the role of AGRN in thyroid cancer (TC) development and progression.
- To analyze AGRN expression levels in various TC subtypes and cell lines.
- To evaluate the impact of AGRN on TC cell behavior and its association with immune infiltration.
Main Methods:
- Analysis of AGRN expression in TC cell lines (CGTH, FTC-133, BcPAP) and patient transcriptomic data.
- In vitro assays including migration, invasion, viability, and proliferation assays.
- Western blot analysis for epithelial-mesenchymal transition (EMT) markers and immunocytochemistry for AGRN localization.
Main Results:
- AGRN expression was significantly elevated in thyroid tumors and TC cell lines, particularly in follicular and papillary subtypes.
- Nuclear localization of AGRN was observed in both normal and TC cells.
- Silencing AGRN diminished TC cell viability, proliferation, migration, and invasion, accompanied by altered expression of EMT markers (vimentin, N-cadherin, E-cadherin).
- Elevated AGRN expression correlated with increased neutrophil infiltration in thyroid tumors.
Conclusions:
- Increased AGRN expression promotes tumorigenic phenotypes in thyroid cancer cells.
- AGRN expression is associated with immune infiltration in thyroid tumors.
- AGRN represents a potential therapeutic target for thyroid cancer, warranting further investigation.
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