Exome Sequencing of Head and Neck Squamous Cell Carcinoma Reveals Inactivating Mutations in NOTCH1
Howard Hughes Medical Institute · Johns Hopkins University · +5 more institutions
Abstract
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide. To explore the genetic origins of this cancer, we used whole-exome sequencing and gene copy number analyses to study 32 primary tumors. Tumors from patients with a history of tobacco use had more mutations than did tumors from patients who did not use tobacco, and tumors that were negative for human papillomavirus (HPV) had more mutations than did HPV-positive tumors. Six of the genes that were mutated in multiple tumors were assessed in up to 88 additional HNSCCs. In addition to previously described mutations in TP53, CDKN2A, PIK3CA, and HRAS, we identified mutations in FBXW7 and NOTCH1. Nearly 40% of the 28 mutations…
Citation impact
- FWCI
- 64.38
- Percentile
- 100%
- References
- 24
Authors
31- NANishant AgrawalCorresponding
Howard Hughes Medical Institute, Johns Hopkins University, Johns Hopkins Medicine, Sidney Kimmel Cancer Center
- MJMitchell J. FrederickCorresponding
The University of Texas MD Anderson Cancer Center
- CRCurtis R. PickeringCorresponding
The University of Texas MD Anderson Cancer Center
- CBChetan BettegowdaCorresponding
Howard Hughes Medical Institute, Johns Hopkins University, Johns Hopkins Medicine, Sidney Kimmel Cancer Center
- KCKyle Chang
Baylor College of Medicine
Topics & keywords
- Exome sequencing
- Head and neck
- Exome
- Head and neck squamous-cell carcinoma
- Head and neck cancer
- Basal cell
- Mutation
- Medicine
- Good health and well-being