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Un interruptor de identidad celular permite que el BCC residual sobreviva a la inhibición de la vía de Hedgehog
Brian Biehs1, Gerrit J P Dijkgraaf1, Robert Piskol2
1Department of Molecular Oncology, Genentech, San Francisco, CA, USA.
Nature
|October 10, 2018
Resumen
Los inhibidores de la vía del erizo como el vismodegib pueden dejar tumores residuales de carcinoma basocelular (BCC) que vuelven a crecer. Estos BCC residuales cambian a una identidad similar a la de las células madre, evitando el tratamiento.
Área de la Ciencia:
- En el campo de la oncología
- Dermatología
- Biología molecular
Sus antecedentes:
- El carcinoma basocelular (BCC) a menudo se trata con inhibidores de la vía del erizo.
- La enfermedad residual y la recaída pueden ocurrir después de la interrupción del tratamiento.
- La comprensión de los mecanismos de resistencia es crucial para el tratamiento eficaz del CBC.
Objetivo del estudio:
- Para investigar el comportamiento de los tumores de carcinoma basocelular residual (BCC) después del tratamiento con el inhibidor Smoothened vismodegib.
- Elucidar los mecanismos celulares y moleculares subyacentes a la resistencia al tratamiento en el CBC.
- Identificar las posibles estrategias terapéuticas para superar la resistencia.
Principales métodos:
- Se utilizó un modelo de ratón Ptch1-Trp53 de carcinoma basocelular (BCC).
- Vismodegib administrado para tratar tumores y enfermedades residuales observadas.
- Se realizó un perfil de transcripción para comparar los BCC residuales y los no tratados.
- Investigamos el estado de la cromatina, la activación de la vía Wnt y la reprogramación del super potenciador.
Principales resultados:
- El tratamiento con vismodegib dio lugar a BCC residuales en reposo que volvieron a crecer al dejar de tomar el medicamento.
- Los BCC residuales adoptaron un programa de transcripción similar al de la epidermis interfolílica y las células madre del istmo.
- Este cambio de identidad involucró la cromatina permisiva, la activación de la vía Wnt y la reprogramación del super potenciador.
- El tratamiento combinado con vismodegib y un inhibidor de la vía Wnt redujo la carga tumoral residual y promovió la diferenciación.
Conclusiones:
- Las células tumorales pueden evadir el tratamiento con vismodegib adoptando una identidad alternativa similar a la de las células madre.
- Este mecanismo de resistencia evita la dependencia del factor oncogénico original.
- Dirigirse tanto a las vías de Hedgehog como a las de Wnt puede ofrecer una estrategia para mejorar la eficacia del tratamiento del CBC y prevenir la recaída.
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