Structural biology and drug discovery targeting oncogenic EGFR and BRAF kinases

Information

  • Research Project
  • 10219986
  • ApplicationId
    10219986
  • Core Project Number
    R50CA221830
  • Full Project Number
    5R50CA221830-05
  • Serial Number
    221830
  • FOA Number
    PAR-17-049
  • Sub Project Id
  • Project Start Date
    9/19/2017 - 6 years ago
  • Project End Date
    8/31/2022 - a year ago
  • Program Officer Name
    AMIN, ANOWARUL
  • Budget Start Date
    9/1/2021 - 2 years ago
  • Budget End Date
    8/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    05
  • Suffix
  • Award Notice Date
    8/31/2021 - 2 years ago

Structural biology and drug discovery targeting oncogenic EGFR and BRAF kinases

Project Summary The Eck laboratory at the Dana-Farber Cancer Institute studies the structure and regulation of oncogenic protein kinases. We apply our unique structural and mechanistic insights in collaborative drug discovery efforts to develop inhibitors with novel mechanisms of action and with selectivity for mutant kinases. The Research Specialist is an expert in structural biology (primarily X-ray crystallography), protein biochemistry and ligand- binding studies, enzyme kinetics, and computational approaches (including virtual ligand screening) and has extensive experience applying these approaches in studies of protein kinases. She is driving our research program in two major areas of interest: 1) development of mutant-selective inhibitors of epidermal growth factor receptor (EGFR) mutants in lung adenocarcinoma, and 2) the structure, regulation, and mechanism of oncogenic activation of BRAF, which is relevant to many cancers. In our studies of these kinases, we seek to understand at a structural level how the activity of the kinase is normally regulated and how this regulation is subverted by oncogenic mutations. With our collaborators in medicinal chemistry and cellular pharmacology, the Research Specialist is developing inhibitors that are effective against EGFR mutants that are resistant to all current targeted therapies, including exon 20 insertion variants of EGFR and EGFR bearing both the T790M and C797S secondary resistance mutations. In addition, the Research Specialist is working to determine the three-dimensional structure of intact BRAF in an autoinhibited state. This work will show how diverse oncogenic mutations lead to BRAF activation and elucidate the mechanism by which many BRAF-targeted drugs induce paradoxical activation of the wild type kinase. In addition, it can be expected to open new avenues for development of BRAF inhibitors that do not exhibit paradoxical activation, and may therefore be effective in the KIAA1549:BRAF truncation fusion found in pediatric brain cancers.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R50
  • Administering IC
    CA
  • Application Type
    5
  • Direct Cost Amount
    105850
  • Indirect Cost Amount
    82563
  • Total Cost
    188413
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    396
  • Ed Inst. Type
  • Funding ICs
    NCI:188413\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZCA1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    DANA-FARBER CANCER INST
  • Organization Department
  • Organization DUNS
    076580745
  • Organization City
    BOSTON
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    022155450
  • Organization District
    UNITED STATES