Oclatinib: alternativa terapéutica para el hemangioma cutáneo canino

Authors

  • María José Tintel Astigarraga
  • Romina Marini Benítez
  • Carlos Alberto Conversso

DOI:

https://doi.org/10.34117/bjdv10n7-042

Keywords:

oclacitinib, canino, hemangioma, neoplasia

Abstract

Los hemangiomas cutáneos son tumores que se originan en las células endoteliales de la pared de los vasos sanguíneos, muy frecuente en caninos. Son predisponentes los animales con pelo corto y claro. Debido a la naturaleza de la neoplasia, la hemorragia local es el problema más frecuente e intolerable para los tutores y pacientes, por eso la resolución quirúrgica es el tratamiento de elección, con alta tasa de reincidencia. La patogenia del HC no se conoce bien; sin embargo, tanto la vasculogénesis como la angiogénesis se asocian con la génesis del hemangioma. La presente revisión proporciona una visión general integrada sobre la naturaleza del hemangioma, factores de señalización de la génesis neoplásica vascular y los factores de crecimiento endotelial vascular asociados con la neovascularización y la génesis del hemangioma. Lo cual, permite comprender la respuesta terapéutica de un canino con múltiples hemangiomas cutáneos tratado con oclacitinib; fármaco que inhibe preferentemente JAK1/ JAK2, y otras quinasas no JAK entre los cuales se menciona 41% de inhibición del receptor 2 del factor de crecimiento endotelial vascular (VEGFR-2/FLK1), el cual es una de las vías desregularizadas en el hemangioma. Enfatizando el conocimiento de las vías de señalización tumoral, se planean alternativas terapéuticas conservadoras con el Oclacitinib como potencial "interruptor angiogénico". Éste es el primer estudio que señala el beneficio clínico y la eficacia de oclacitinib en perros con neoformación vascular cutánea.

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Published

2024-07-23

How to Cite

Astigarraga, M. J. T., Benítez, R. M., & Conversso, C. A. (2024). Oclatinib: alternativa terapéutica para el hemangioma cutáneo canino. Brazilian Journal of Development, 10(7), e71425. https://doi.org/10.34117/bjdv10n7-042

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Section

Original Papers