| Literature DB >> 23233526 |
Barbara Burtness1, Shanthi Marur, Julie E Bauman, Erica A Golemis, Ranee Mehra, Steven J Cohen.
Abstract
Epidermal growth factor receptor (EGFR) and mammalian target of rapamycin (mTOR) play important roles in tumor growth, which has stimulated efforts toward the design of targeted cancer therapeutics that inhibit their function. A growing body of literature indicates that EGFR and mTOR are also essential to support a functional innate immune response. Hence, although combination therapies that block both EGFR and mTOR may have improved activity against tumors, they may also place patients at risk of fulminant infections. We discuss data supporting this hypothesis.Entities:
Mesh:
Substances:
Year: 2012 PMID: 23233526 DOI: 10.1126/scisignal.2003734
Source DB: PubMed Journal: Sci Signal ISSN: 1945-0877 Impact factor: 8.192