TELOMERASE AND TELOMERE DYNAMICS IN CANCER AND AGING

Information

  • Research Project
  • 6189398
  • ApplicationId
    6189398
  • Core Project Number
    R13AG019083
  • Full Project Number
    1R13AG019083-01
  • Serial Number
    19083
  • FOA Number
  • Sub Project Id
  • Project Start Date
    7/1/2000 - 24 years ago
  • Project End Date
    6/30/2001 - 23 years ago
  • Program Officer Name
    MCCORMICK, ANNA M.
  • Budget Start Date
    7/1/2000 - 24 years ago
  • Budget End Date
    6/30/2001 - 23 years ago
  • Fiscal Year
    2000
  • Support Year
    1
  • Suffix
  • Award Notice Date
    6/26/2000 - 24 years ago
Organizations

TELOMERASE AND TELOMERE DYNAMICS IN CANCER AND AGING

The telomere-telomerase hypothesis of aging and cancer implicates telomere length and telomerase as regulators of replicative senescence and cellular immortality. In support of this hypothesis, telomeres have been shown to shorten with cellular senescence in vitro and with aging in vivo, telomerase expression is detected in tumor cells but not in most normal cells, and telomerase inhibition leads to telomere shortening and eventually cell crisis and apoptosis in tumor cells. Significant advances have made it possible to experimentally test many aspects of this hypothesis. These include the cloning of the telomerase RNA and protein components, telomerase associated proteins, telomere binding proteins, telomerase and telomere assays, and the discovery of both positive and negative regulators of telomere dynamics. Further understanding of the pathways connecting telomere shortening, cellular senescence, telomerase and cancer will have significant impact on the development of novel therapeutic approaches for cancer and age-related diseases. The proposed symposium will focus in depth on the most rapidly emerging areas in the field of telomere and telomerase biology. The advent of research on telomerase and telomere dynamics in pluripotent stem cell biology and mammalian cloning through nuclear transfer experiments adds a new dimension to this meeting. Special emphasis would be placed on studies relevant to the aging disciplines as well as those which explore the relationships between cancer and aging. The symposium will consist of formal sessions that will include both invited and contributed presentations. In addition to having highly regarded scientists who have already accepted to participate, additional invited speakers and time slots will be available for speakers selected from submitted abstracts and for those with late-breaking results. There will be formal sessions each morning and evening and informal time each afternoon for posters and to facilitate interactions. This meeting will, therefore, bring together both basic scientists investigating telomere/telomerase biology and clinicians interested in fundamental aging and cancer mechanisms, to present new discoveries and to discuss the most late-breaking findings.

IC Name
NATIONAL INSTITUTE ON AGING
  • Activity
    R13
  • Administering IC
    AG
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    15000
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    866
  • Ed Inst. Type
  • Funding ICs
    NCI:5000\NIA:10000\
  • Funding Mechanism
  • Study Section
    ZCA1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    GERON CORPORATION
  • Organization Department
  • Organization DUNS
  • Organization City
    MENLO PARK
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    940251109
  • Organization District
    UNITED STATES