Association of BRAF V600E Mutant Allele Proportion with the Dissemination Stage of Papillary Thyroid Cancer

Author:

Blazekovic Ivan12,Samija Ivan13ORCID,Perisa Josipa1ORCID,Gall Troselj Koraljka4ORCID,Regovic Dzombeta Tihana56ORCID,Radulovic Petra5,Romic Matija1,Granic Roko1,Sisko Markos Ines12ORCID,Frobe Ana13,Kusic Zvonko7,Jukic Tomislav168

Affiliation:

1. Department of Oncology and Nuclear Medicine, University Hospital Center Sestre Milosrdnice, 10 000 Zagreb, Croatia

2. School of Medicine, Catholic University of Croatia, 10 000 Zagreb, Croatia

3. School of Dental Medicine, University of Zagreb, 10 000 Zagreb, Croatia

4. Laboratory for Epigenomics, Division of Molecular Medicine, Ruđer Bošković Institute, 10 000 Zagreb, Croatia

5. Department of Pathology Ljudevit Jurak, University Hospital Center Sestre Milosrdnice, 10 000 Zagreb, Croatia

6. School of Medicine, University of Zagreb, 10000 Zagreb, Croatia

7. Croatian Academy of Science and Arts, 10000 Zagreb, Croatia

8. Faculty of Medicine Osijek, Josip Juraj Strossmayer University of Osijek, 31 000 Osijek, Croatia

Abstract

The early identification of aggressive forms of cancer is of high importance in treating papillary thyroid cancer (PTC). Disease dissemination is a major factor influencing patient survival. Mutation status of BRAF oncogene, BRAF V600E, is proposed to be an indicator of disease recurrence; however, its influence on PTC dissemination has not been deciphered. This study aimed to explore the association of the frequency of BRAF V600E alleles in PTC with disease dissemination. In this study, 173 PTC samples were analyzed, measuring the proportion of BRAF V600E alleles by qPCR, which was then normalized against the proportion of tumor cells. Semiquantitative analysis of BRAF V600E mutant protein was performed by immunohistochemistry. The BRAF V600E mutation was present in 60% of samples, while the normalized frequency of mutated BRAF alleles ranged from 1.55% to 92.06%. There was no significant association between the presence and/or proportion of the BRAF V600E mutation with the degree of PTC dissemination. However, the presence of the BRAF mutation was significantly linked with angioinvasion. This study’s results suggest that there is a heterogeneous distribution of the BRAF mutation and the presence of oligoclonal forms of PTC. It is likely that the BRAF mutation alone does not significantly contribute to PTC aggressiveness.

Funder

Croatian Science Foundation

Publisher

MDPI AG

Reference50 articles.

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