Artículo
Current concepts in ameloblastoma-targeted therapies in B-raf proto-oncogene serine/threonine kinase V600E mutation: Systematic review
Fecha
2020Registro en:
González-González, R, López-Verdín, S, Lavalle-Carrasco, J, y otros. "Current concepts in ameloblastoma-targeted therapies in B-raf proto-oncogene serine/threonine kinase V600E mutation: Systematic review". World Journal Clinical Oncology. [en línea] January 24; 11(1): 31-42, 2020. DOI: 10.5306/wjco.v11.i1.31
2218-4333 (online)
DOI: 10.5306/wjco.v11.i1.31
Autor
González-González, Rogelio
López-Verdín, Sandra
Lavalle-Carrasco, Jesús
Molina-Frechero, Nelly
Isiordia-Espinoza, Mario
Carreón Burciaga, Ramón Gil
Bologna-Molina, Ronell
Institución
Resumen
Ameloblastomas are common benign epithelial odontogenic neoplasms that
present an aggressive and unpredictable behavior that may modify treatment
strategies. Different signaling pathways that participate in the progression of
these tumors have been identified. B-raf proto-oncogene serine/threonine kinase
(BRAF) is a protein involved in the behavior of ameloblastomas, and it is related
to many cell mechanisms. BRAF gene mutations have been identified in
ameloblastomas, of which the BRAF V600E (valine substituted by glutamic acid
at amino acid 600) mutation has been the most common and can be present
concomitantly with other mutations that may be involved in its behavior.
Targeted therapies have been used as an alternative in the case of resistance or
contraindications to conventional treatments.