Systems Modeling Identifies Divergent Receptor Tyrosine Kinase Reprogramming to MAPK Pathway Inhibition
Abstract
Introduction: Targeted cancer therapeutics have demonstrated more limited clinical efficacy than anticipated, due to both intrinsic and acquired drug resistance. Underlying mechanisms have been largely attributed to genetic changes, but a substantial proportion of resistance observations remain unexplained by genomic properties. Emerging evidence shows that receptor tyrosine kinase (RTK) reprogramming is a major alternative process causing targeted drug resistance, separate from genetic alterations. Hence, the contributions of mechanisms leading to this process need to be more rigorously assessed.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jul 26, 2018
- Accession Number
- AD1083385
Entities
People
- Aaron S. Meyer
- Allison M. Claas
- Douglas A. Lauffenburger
- Lyla Atta
- Simon Gordonov
Organizations
- Massachusetts Institute of Technology