The Relation of TSH Receptor Polymorphism to The Behavior of Papillary Thyroid Carcinoma in Egyptian Population

Document Type : Original Article

Authors

1 Endocrinology Unit, Department of Internal Medicine, Faculty of Medicine, Alexandria University, Alexandria, Egypt

2 Department of Clinical Pathology, Faculty of Medicine, Alexandria University, Alexandria, Egypt

3 Head, Neck and Endocrine Surgery Unit, Department of Surgery, Faculty of Medicine, Alexandria University, Alexandria, Egypt

4 Department of Pathology, Faculty of Medicine, Alexandria University, Alexandria, Egypt

Abstract

Background: Thyroid cancer is the most common endocrine cancer, in which genetic mutations play a major role. We studied thyroid stimulating hormone (TSH) receptor gene polymorphism (rs179247 and rs12101255) in papillary thyroid carcinoma (PTC).

Methods: The study was conducted on fifty patients with documented PTC. Patients with thyroid nodules were selected from Alexandria University hospital outpatient clinics after excluding hyperthyroidism, autoimmune thyroid diseases, and non-suspicious nodules. Eligible patients were subjected to total thyroidectomy in the head and neck and endocrine surgery unit. DNA, extracted from formalin fixed paraffin embedded normal and malignant thyroid tissues, was analyzed by real time polymerase chain reaction using TaqMan® Genotyping Assay.

Results: No difference was found between normal and malignant tissues regarding TSH receptor polymorphism. No relations were found in both polymorphisms with serum TSH, malignant nodule size, multiplicity of the lesions, TIRADs staging, or Bethesda classification. Rs179247 genotype AA (vs. AG and GG: P=0.044*) was associated with extrathyroidal extension.

Conclusions: In conclusion TSH receptor polymorphism rs179247, and not rs12101255, may predict extrathyroidal extension in papillary thyroid cancer.

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Zagazig University Medical Journal
Volume 31, Issue 2
February 2025
Pages 922-929

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