Structure-activity relationship study of an inhibitor of tumor metastasis

Information

  • Research Project
  • 7480179
  • ApplicationId
    7480179
  • Core Project Number
    R43CA134102
  • Full Project Number
    1R43CA134102-01
  • Serial Number
    134102
  • FOA Number
    PA-07-80
  • Sub Project Id
  • Project Start Date
    9/12/2008 - 16 years ago
  • Project End Date
    2/28/2010 - 14 years ago
  • Program Officer Name
    COTTON, PAUL
  • Budget Start Date
    9/12/2008 - 16 years ago
  • Budget End Date
    2/28/2010 - 14 years ago
  • Fiscal Year
    2008
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/12/2008 - 16 years ago

Structure-activity relationship study of an inhibitor of tumor metastasis

[unreadable] DESCRIPTION (provided by applicant): A large number of deaths from epithelial tumors of the breast, prostate, lung, ovary, liver, and kidney are caused by metastatic spread of the primary tumor. Unfortunately, there are currently no drugs on the market that directly target cancer cells in the process of spreading (metastasis). The tumor antigen, sialyl Lewis X (sLeX) is a glycan expressed on the surface of epithelial tumors that correlates with poor prognosis, aggressive metastasis, and death. In both human and animal studies sLeX expression can drive aggressive metastatic behavior (1-5). We have rationally designed an inhibitor of sLeX biosynthesis that potently blocks metastasis in mouse models (6-11). The following aims are focused on a structure-activity relationship study of our lead compound. PUBLIC HEALTH RELEVANCE: A large number of deaths from cancer of the breast, prostate, lung, ovary, liver, and kidney are caused by metastatic spread of the primary tumor. The medical need for an effective anti-metastatic drug is great. These studies are aimed at optimizing an anti-metastatic drug candidate before human clinical trials. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    188112
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    395
  • Ed Inst. Type
  • Funding ICs
    NCI:188112\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ZACHARON PHARMACEUTICALS, INC.
  • Organization Department
  • Organization DUNS
    068188411
  • Organization City
    San Diego
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    92121
  • Organization District
    UNITED STATES