Epigenetic EGFR Gene Repression Confers Sensitivity to Therapeutic BRAFV600E Blockade in Colon Neuroendocrine Carcinomas.
Jaume CapdevilaOriol ArquésJose Ramón Hernández MoraJudit MatitoGinevra CaratùFrancesco M MancusoStefania LandolfiJorge BarriusoPaula Jiménez-FonsecaCarlos López LópezRocio Garcia-CarboneroJorge HernandoIgnacio MatosNuciforo PaoloJavier Hernández-LosaManel EstellerAnna Martínez-CardúsJosep TaberneroAna VivancosHéctor G PalmerPublished in: Clinical cancer research : an official journal of the American Association for Cancer Research (2019)
The identification of V600E BRAF mutations in high-grade co-NECs has allowed the description of radiological responses to combination therapy of BRAF and MEK inhibitors in basket clinical trials. However, the molecular rationale for this treatment combination was based on the presence of the BRAF mutation and the efficacy observed in other cancer types such as melanoma. Future drug development in this setting should test BRAF inhibitors upfront and the addition of anti-EGFR antibodies instead of MEK inhibitors for an efficient blockade of acquired resistance.
Keyphrases
- combination therapy
- high grade
- metastatic colorectal cancer
- clinical trial
- small cell lung cancer
- wild type
- epidermal growth factor receptor
- tyrosine kinase
- low grade
- dna methylation
- pi k akt
- papillary thyroid
- gene expression
- genome wide
- squamous cell carcinoma
- squamous cell
- current status
- cell proliferation
- study protocol
- smoking cessation
- genome wide identification
- transcription factor