| Literature DB >> 25855404 |
Frank B Furnari1, Timothy F Cloughesy2, Webster K Cavenee3, Paul S Mischel1.
Abstract
As tumours evolve, the daughter cells of the initiating cell often become molecularly heterogeneous and develop different functional properties and therapeutic vulnerabilities. In glioblastoma (GBM), a lethal form of brain cancer, the heterogeneous expression of the epidermal growth factor receptor (EGFR) poses a substantial challenge for the effective use of EGFR-targeted therapies. Understanding the mechanisms that cause EGFR heterogeneity in GBM should provide better insights into how they, and possibly other amplified receptor tyrosine kinases, affect cellular signalling, metabolism and drug resistance.Entities:
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Year: 2015 PMID: 25855404 PMCID: PMC4875778 DOI: 10.1038/nrc3918
Source DB: PubMed Journal: Nat Rev Cancer ISSN: 1474-175X Impact factor: 60.716