The lab utilizes a multitude of strategies to identify critical pathways required to promote tumorigenesis. These include high-throughput bioinformatics and structural modelling, siRNA screening, and precision genome editing to establish various functional genomic approaches to identify novel drivers. Utilizing bioinformatics we identify novel kinases enriched for functional mutations to hone in on activated enzymes that can serve as drug targets. We then assess the structural consequences of a subset of mutations in the respective kinases, where crystal structures are available, to determine if the mutations likely increase or decrease catalytic activity. These approaches have been successful in identifying kinases with activating mutations in lung cancer (ABL1 - Testoni et al EMBO Mol. Med.). Going forward we are focused on novel drivers of the 3q amplicon that play a critical role in promoting tumorigenesis in lung squamous cell carcinoma, head and neck cancer, and ovarian cancer (Edwards et al Cancer Research). These novel drivers can serve as targets of therapeutic intervention and an intense effort will focused on the mechanisms by which these amplified kinases or kinases that harbor GOF mutations promote tumorigenesis. In addition, we are studying a novel kinase target that represents a genetic dependency in KRAS mutant lung adenocarcinomas and promotes resistance to ERK inhibitor therapies in melanoma.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIABC011691-03
Application #
9780005
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Basic Sciences
Department
Type
DUNS #
City
State
Country
Zip Code
Torres-Ayuso, Pedro; Sahoo, Sudhakar; Ashton, Garry et al. (2018) Signaling pathway screening platforms are an efficient approach to identify therapeutic targets in cancers that lack known driver mutations: a case report for a cancer of unknown primary origin. NPJ Genom Med 3:15
Edwards, Zoe C; Trotter, Eleanor W; Torres-Ayuso, Pedro et al. (2017) Survival of Head and Neck Cancer Cells Relies upon LZK Kinase-Mediated Stabilization of Mutant p53. Cancer Res 77:4961-4972
Testoni, Ewelina; Stephenson, Natalie L; Torres-Ayuso, Pedro et al. (2016) Somatically mutated ABL1 is an actionable and essential NSCLC survival gene. EMBO Mol Med 8:105-16
Antal, Corina E; Hudson, Andrew M; Kang, Emily et al. (2015) Cancer-associated protein kinase C mutations reveal kinase's role as tumor suppressor. Cell 160:489-502