2017, Número 1
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Biotecnol Apl 2017; 34 (1)
Citotoxicidad celular dependiente de anticuerpos inducida por el nimotuzumab en líneas tumorales depende de los niveles de expresión del receptor del factor de crecimiento epidérmico humano
Chao L, Pérez D, Sánchez B
Idioma: Ingles.
Referencias bibliográficas: 32
Paginas: 1201-1205
Archivo PDF: 539.27 Kb.
RESUMEN
El receptor del factor de crecimiento epidérmico humano (EGFR) se ha convertido en uno de los blancos más atractivos para el tratamiento del cáncer, debido a su papel trascendental en el desarrollo tumorigénico. Nimotuzumab es un anticuerpo monoclonal (mAb) específico contra el dominio extracelular del EGFR, del cual inhibe su cascada de señalización y arresta el ciclo celular en células tumorales de origen epitelial. Es conocido que la citoxicidad celular dependiente de anticuerpo (ADCC) es un mecanismo que contribuye a la efectividad clínica de algunas drogas terapéuticas antitumorales. Sin embargo, no existen reportes sobre la posible ocurrencia de respuesta ADCC mediada por el nimotuzumab y su relevancia para el efecto antitumoral. Por tales razones, en este estudio se analizó la capacidad del nimotuzumab de inducir respuesta ADCC y la influencia de los niveles de expresión del EGFR en dicho mecanismo de acción. Se demostró que este mAb induce ADCC en células tumorales en cultivo, la cual se incrementa con el aumento en la concentración del anticuerpo y es dependiente de los niveles de EGFR. Estos resultados sugieren que la ADCC puede ser uno de los mecanismos potenciales a través de los cuales el nimotuzumab ejerce su efecto terapéutico en pacientes con tumores de alta expresión del EGFR.
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