Searchable abstracts of presentations at key conferences in endocrinology

ea0092ps1-01-01 | Cancer | ETA2023

Impact of the 3rd edition of bethesda system for reporting thyroid cytopathology on grey zone categories

Guerreiro Sofia , Baran Yunus , Tavares Paula , Pinto Marques Hugo , Bongiovanni Massimo , Canberk Sule

First TBSRTC editions have made advances in problems of thyroid management. However, the real grey zone ‘AUS/FLUS’ and ‘FN/SFN’categories have been remained to be problematic with the wide range of ROMs documented in the literature alongside two editions. The ROMs of ‘AUS/FLUS’ and ‘FN/SFN’ categories were defined as 5-15% and 15-30% and the management was ‘repeat FNA’ and ‘lobectomy’ -respectively- in the first editi...

ea0092ps3-28-08 | Translational 2 | ETA2023

Understanding the putative role OF ACE2, TMPRSS2 and furin proteins on thyroid neoplastic transformation

Teresa Azevedo Maria , Macedo Sofia , Canberk Sule , Batista Rui , Soares Paula

Angiotensin-converting enzyme 2 (ACE2), Transmembrane serine protease 2 (TMPRSS2) and Furin were known to be key players for the SARS-CoV-2 infection. Thyroid gland was shown to be one of the relevant targets for SARS-CoV-2 infection allegedly due to the higher expression levels of these molecules in follicular cells. However, it remains to be fully determined the expression of ACE2, TMPRSS2 and Furin in normal follicular cell. In addition, the putative role of these molecules...

ea0084op-07-33 | Oral Session 7: Thyroid Cancer Basic | ETA2022

HüRthle cell tumors vs oncocytic variants of the follicular cell derived thyroid tumours: a comprehensive analysis based in transcriptome, proteome and cnv profiling

Canberk Sule , ferreira marta , Oliveira Carla , reis joana , barros rita , pereira luisa , osorio hugo , Rios Elisabete , Soares Paula , Maximo Valdemar

Objectives: Hürthle cell (oncocytic) lesions can be metaplastic or neoplastic events. The neoplastic entities -formerly, oncocytic variant of follicular tumours; Hürthle cell neoplasm (HCN) - include HC adenomas and HC carcinomas and have been recognized as a separate class of tumours by the WHO. The remaining of the thyroid tumours demonstrating “mitochondrion-rich cells” and oncocytic morphology are referred under the umbrella term of “oncocytic vari...

ea0092ps1-08-06 | Translational 1 | ETA2023

Comparative cyto-histological genetic profile in a series of differentiated thyroid carcinomas

De Lurdes Godinho De Matos Maria , Pinto Mafalda , Alves Marta , Canberk Sule , Luisa Papoila Ana , Joao Bugalho Maria , Soares Paula

Introduction: Ultrasound-guided fine-needle aspiration cytology (US-FNAC), the gold standard method to distinguish benign from malignant thyroid nodules, is the most accurate, cost-effective and minimal invasive preoperative test, aiming to resolve patient management. However, up to 30% of US-FNACs are classified as indeterminate nodules, making difficult to avoid unnecessary surgeries. Molecular tests may contribute to refine the preoperative diagnosis of thyroid nodules....

ea0092ps1-08-08 | Translational 1 | ETA2023

The role of micrornas to the diagnosis of differentiated thyroid carcinomas

De Lurdes Godinho De Matos Maria , Pinto Mafalda , Alves Marta , Canberk Sule , Joao Bugalho Maria , Luisa Papoila Ana , Soares Paula

Introduction: Several studies recommend the use of molecular tests for a complete diagnosis of malignancy in thyroid carcinomas (TC). The study and identification of molecular markers in thyroid will contribute to a personalized and effective treatment of the patients. The development of TC has been associated with the activation of oncogenes that are implicated in the cell signaling pathway, interfering in cancer promotion and outcome. Moreover, the repertoire of microRNAs (m...

ea0084ps2-10-95 | Nodules & Cancer | ETA2022

Contribution of cyto-histological genetic profile to a precocious diagnosis in thyroid neoplasm

De Lurdes Godinho De Matos Maria , pinto mafalda , Alves Marta , Canberk Sule , Boaventura Paula , Goncalves Ana , Luisa Papoila Ana , Joao Bugalho Maria , Soares Paula

Introduction: The diagnostic gold standard for thyroid nodular disease is ultrasound-guided fine-needle aspiration cytology (US-FNAC), being the most accurate, cost-effective and minimal invasive preoperative test to distinguish benign from malignant nodules, aiming to resolve patient management. However, up to 30% of FNACs are classified as indeterminate nodules, turning difficult the decision on patient management to avoid unnecessary surgeries. The development of thyroid ca...

ea0092op-12-02 | Oral Session 12: Emerging Insights into Thyroid Cancer Genetics | ETA2023

Comparative analysis of somatic copy number alterations (SCNA) between hürthle cell tumors (HCT) and oncocytic variant of follicular cell derived thyroid tumors (OV-FCDTT)

Canberk Sule , Ferreira Marta , Oliveira Carla , Reis Joana , Barros Rita , Pereira Luisa , Osorio Hugo , Rios Elisabete , Paula Arnaud , Soares Paula , Maximo Valdemar

Objectives: Somatic copy number alterations (SCNAs) have been the most common genetic alterations identified in cancer, that frequently related with extensive genomic instability and to an aggressive behavior. Hürthle cell carcinoma is known to be aggressive, having the highest incidence of recurrences, distant metastasis and RAI therapy resistance among all differentiated follicular cell derived thyroid carcinomas. Due to these differences and recent molecular discoverie...

ea0092op-12-04 | Oral Session 12: Emerging Insights into Thyroid Cancer Genetics | ETA2023

Genetics of familial non-medullary thyroid carcinoma - investigation of two families’

Teixeira Elisabete , Fernandes Claudia , Gaspar Tiago , Ferreira Marta , Lima Raquel , Canberk Sule , Prazeres Hugo , Soares Paula , Rodrigues Fernando , Martins Teresa , Fernandes Andreia

Introduction: By Next Generation Sequencing (NGS) our team identified in two families presenting a phenotype compatible with familial non-medullary thyroid carcinoma (Family C and Family R), two new potentially pathogenic germline mutations. Family C presented p.Gly106Arg mutation in the KCNB2 gene, that codifies a voltage-gated potassium channel (vgKCN). Since potassium efflux by the cell is a necessary condition for cellular homeostasis, vgKCN disruption can impact the funct...