ETA2022 Poster Presentations Thyroid Cancer BASIC (10 abstracts)
1Institute for the Application of Nuclear Energy Inep, Department for Endocrinology and Radioimmunology, University of Belgrade, Institute for the Application of Nuclear Energy Inep, University of Belgrade, Belgrade, Serbia, Institute for the Application of Nuclear Energy Inep, University of Belgrade, Belgrade, Serbia, Belgrade, Serbia; 2Institute for the Application of Nuclear Energy Inep, University of Belgrade, Belgrade, Serbia, Serbia; 3Institute for the Application of Nuclear Energy Inep, University of Belgrade, Department for Endocrinology and Radioimmunology, Belgrade, Serbia; 4Center for Endocrine Surgery, Institute of Endocrinology, Diabetes and Diseases of Metabolism, Clinical Center of Serbia, Belgrade, Serbia, 3center for Endocrine Surgery, Institute of Endocrinology, Diabetes and Diseases of Metabolism, Clinical Center of Serbia, Belgrade, Serbia; 5Institute of Pathology, Faculty of Medicine, University of Belgrade, Serbia, Serbia
Objectives: Finding novel tumor markers capable to recognize aggressive papillary thyroid carcinoma (PTC) forms are of great importance. We evaluated hsa-microRNA-204-3p (miR-204-3p) for differential diagnosis of thyroid tumors and assessed its prognostic usefulness.
Methods: MiR-204-3p levels were determined in 77 PTC cases of diverse histological variants, 12 cases of follicular thyroid adenoma (FTA), and 89 matched nonmalignant thyroid epithelial tissues (NMT) using RT-qPCR. The results were evaluated in comparison with the clinicopathological features of the patients.
Results: The relative expression of miR-204-3p is lower in PTC compared to the levels in paired NMT, with the median down-regulation of 65% (P < 0.05). The level of miR-204-3p down-regulation depends on PTC subtype PTC cases with classical variant architecture had significantly more down-regulated values of miR-204-3p (median down-regulation was 85%) than all other PTC subtypes (median down-regulation in follicular variant was 41%, in cases with mixed architecture 60%, in rare variants, that included Warthin-like, tall cell, solid, clear cell, and oxyphilic cases, was 45%) (P < 0.05). Lower levels of relative miR-204-3p expression in PTC associate with the presence of metastasis to regional lymph nodes, intraglandular tumor dissemination and a degree of tumor infiltration through the gland (P < 0.05). On the other hand, miR-204-3p is up-regulated in FTA (median up-regulation 178%). Up-regulated expression of miR-204-3p is a sensitive (83.3%) and specific (74.7%) marker for distinction of FTA from PTC (cut off=1.08, P < 0.001, AUC=0.821).
Conclusions: MiR-204-3p is a useful marker for PTC detection, particularly its classical variant, and can help in risk stratification of PTC patients.