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A mutation panel comprising BRAFV600E, NRASQ61R, and NRASQ61H replicated retrospective histopathological examination findings in differentiating benign goitre from malignant papillary thyroid cancer in a cohort of Malaysian patients.
Eng, Z H; Ahmad Jefry, M M; Ng, K L; Abdul Aziz, A; Mat Junit, S.
Afiliação
  • Eng ZH; Universiti Malaya, Faculty of Medicine, Department of Molecular Medicine, 50603 Kuala Lumpur, Malaysia.
  • Ahmad Jefry MM; Universiti Malaya, Faculty of Medicine, Department of Molecular Medicine, 50603 Kuala Lumpur, Malaysia.
  • Ng KL; Universiti Malaya, Faculty of Medicine, Department of Surgery, 50603 Kuala Lumpur, Malaysia.
  • Abdul Aziz A; Universiti Malaya, Faculty of Medicine, Department of Molecular Medicine, 50603 Kuala Lumpur, Malaysia.
  • Mat Junit S; Universiti Malaya, Faculty of Medicine, Department of Molecular Medicine, 50603 Kuala Lumpur, Malaysia. sarni@um.edu.my.
Malays J Pathol ; 45(3): 375-390, 2023 Dec.
Article em En | MEDLINE | ID: mdl-38155379
ABSTRACT
Thyroid malignancy status is usually confirmed through histopathological examination (HPE) following thyroidectomy. In Malaysia, the application of molecular markers in pre-operative diagnosis of thyroid cancer remains unexplored. In this study, BRAF and NRAS gene mutation panel was assessed, and the results were compared with retrospective HPE findings. Malaysian patients with benign goitre (BTG n=33) and papillary thyroid cancer (PTC n=25; PTCa n=20, PTCb n=5) were recruited at Universiti Malaya Medical Centre from September 2019 to December 2022. PCR-direct DNA sequencing of BRAFV600, NRASG12, NRASG13, and NRASQ61 was conducted on DNA extracted from the patients' thyroid tissue specimens following thyroidectomy and HPE. BRAFV600E and NRASQ61R mutations showed absolute PTC-specificity with PTC-sensitivity of 32% and 28%, respectively. NRASQ61H demonstrated lower PTC-specificity (94%) but higher PTC-sensitivity (72%) compared to the BRAFV600E and NRASQ61R mutations. Although the NRASG12 and NRASG13 variants were absent in this study, a novel NRASV14D mutation was detected in a PTCa patient. Unlike PTCb, coexistence of BRAFV600E and NRASQ61 variants was commonly observed among the PTCa patients. Notably, all PTCb patients had NRASQ61H mutation with one patient carried both the NRASQ61H and BRAFV600E mutations. Association analysis revealed potential link between gender, BRAFV600E mutation and lymph node metastasis. In conclusion, mutation panel comprising BRAFV600E, NRASQ61R, and NRASQ61H did not discriminate the two PTC subtypes but replicated the retrospective HPE findings in differentiating BTG from PTC. The application of this mutation panel in pre-operative diagnosis of thyroid nodules requires further validation in a larger sample size, preferably incorporating fineneedle aspirate biopsies.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide / Carcinoma Papilar / Bócio Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide / Carcinoma Papilar / Bócio Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article