| Literature DB >> 30380421 |
Christina Karamboulas1, Jeffrey P Bruce1, Andrew J Hope2, Jalna Meens1, Shao Hui Huang2, Natalie Erdmann1, Elzbieta Hyatt3, Keira Pereira1, David P Goldstein4, Ilan Weinreb5, Jie Su6, Brian O'Sullivan2, Rodger Tiedemann1, Fei-Fei Liu7, Trevor J Pugh8, Scott V Bratman7, Wei Xu9, Laurie Ailles10.
Abstract
Overall survival remains very poor for patients diagnosed as having head and neck squamous cell carcinoma (HNSCC). Identification of additional biomarkers and novel therapeutic strategies are important for improving patient outcomes. Patient-derived xenografts (PDXs), generated by implanting fresh tumor tissue directly from patients into immunodeficient mice, recapitulate many of the features of their corresponding clinical cancers, including histopathological and molecular profiles. Using a large collection of PDX models of HNSCC, we demonstrate that rapid engraftment into immunocompromised mice is highly prognostic and show that genomic deregulation of the G1/S checkpoint pathway correlates with engraftment. Furthermore, CCND1 and CDKN2A genomic alterations are predictive of response to the CDK4and CDK6 inhibitor abemaciclib. Overall, our study supports the pursuit of CDK4 and CDK6 inhibitors as a therapeutic strategy for a substantial proportion of HNSCC patients and demonstrates the potential of using PDX models to identify targeted therapies that will benefit patients who have the poorest outcomes.Entities:
Keywords: abemaciclib; cyclin D1; engraftment; head and neck squamous cell carcinoma; patient-derived xenografts; preclinical drug testing
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Year: 2018 PMID: 30380421 DOI: 10.1016/j.celrep.2018.10.004
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423