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DCB - Office of the Director (OD)


Welcome to the World Wide Web Home Page of the Office of the Director of the Division of Cancer Biology (DCB), National Cancer Institute (NCI). This Office integrates the activities of the component Branches by establishing program priorities, allocating resources, and evaluating program effectiveness with the advice of the NCI Board of Scientific Advisors, the National Cancer Advisory Board, and other advisory committees. The NCI Mouse Models of Human Cancers Consortium is also administratively located in the Office of the Director, DCB. DCB is responsible for the federal program of extramural research in cancer biology and associated areas of science and the DCB Director represents these areas and associated issues in management and scientific decision-making meetings within and outside NCI.

DCB supports research primarily through investigator-initiated research grants and it is a priority of DCB to work with and assist individual investigators in presenting their ideas for research in the most effective way. The implementation of the new NCI process of Accelerated Executive Review (AER) for high-quality but unfunded original applications, combined with the new NIH policy limiting the number of amended applications that will be considered for funding, makes it increasingly important to prepare an outstanding application the first time. Please contact our staff for information or to answer questions, and the next time you see our extramural staff at a scientific meeting, please introduce yourself and feel free to ask questions, or just say "hello".



Program Announcements and Request for Application
 PA-03-147 -AGE-RELATED CHANGES IN TISSUE FUNCTION: UNDERLYING BIOLOGICAL MECHANISMS
 
STAFF
NameTitle
 Singer, Dinah, Ph.D. Director
 Sogn, John, Ph.D. Deputy Director
 Marks, Cheryl, Ph.D. Associate Director
 Tarnowski, Betty, Ph.D. Exec. Director, MMHCC
 Brown, Robin Program Specialist
 Hickle, Dan IT Specialist
 Lindsay, Johnny IT Specialist
 Slater, Brian IT Manager
 Wachholz, Bruce, Ph.D. Sr. Coordinator for Int.'l Relations
 White, Stephen Special Assistant/Program Coord.
 Whitehead, Matthew Office Automation Assistant
 Woods, Debra Secretary to the Director




NCI/NIGMS Synchrotron Beamline

A synchrotron beamline for determining structures of proteins and other macromolecules, under joint administration of the National Cancer Institute and the National Institute of General Medical Sciences, will produce its first usable X-rays for crystallography in 2004 and will be fully operational a year later. The Division of Cancer Biology is the lead organization for the National Cancer Institute.

NCI teamed with NIGMS in initiating construction of a synchrotron beamline at the Advanced Photon Source (APS), located at the Department of Energy's Argonne National Laboratory near Chicago. In March 2002, NCI and NIGMS leadership signed a memorandum of understanding with the APS to build beamline facilities. Preliminary design review was approved at the time, clearing the way for construction later this year. The German company ACCEL Instruments is under contract to build the beamline. The construction budget of approximately $18 million will be shared equally between NCI and NIGMS. Once construction is complete, operation costs for the beamline are estimated to be $4 million a year, of which NCI has committed $1 million annually.

NCI and NIGMS grantees will have access to the beam through a peer review process for research projects. Half of the beam time will be allocated to peer-reviewed research, while 25% will be reserved for maintenance and staff use. The remaining 25% would be divided between the two collaborating institutes for "special uses.

A special design feature of the beamline will double the number of usable experiments possible from the beam. Two undulators, which produce the synchrotron radiation in the accelerator loop, will be offset slightly (0.06°) to produce two beams of radiation within the team's research area.

Mouse Models of Human Cancers Consortium

The Mouse Models of Human Cancers Consortium (MMHCC), assembled from multidisciplinary teams of scientists, was established to apply the collective scientific expertise of its members in model design and research on human cancer to derive or refine mouse models of human cancers. The consortium is dedicated to the collaborative development, characterization, and validation of mouse models that are analogs of human cancers. The consortium enables each individual team to pursue its most innovative ideas and experimental approaches and to interact with the other teams within the consortium to foster the rapid exchange of ideas, information, and technology. These activities are further stimulated and facilitated by interactions with the NCI, and enhanced by linkages to key research communities when augmentation of the scientific and technical expertise of the consortium is warranted. The consortium and the NCI work together to implement workshops and symposia, to provide information about the models and related technology, and to plan for distribution of the validated mouse models to the cancer research community.

The models that the MMHCC derives and validates will be made available to the entire research community and should serve to accelerate the pace of discovery of the genetic and epigenetic factors that underlie the initiation of cancer and define the functions of cancer-related genes that promote tumor progression and metastasis. It is expected that these models will be valuable as the means to test new therapeutic, preventive, early detection, and diagnostic imaging strategies. As the MMHCC progresses, NCI will ensure inclusion of additional partners from the academic and private sector research communities through the formation of specialized MMHCC forums. As forums are added to the MMHCC, the Consortium will be able to capitalize rapidly on discoveries in all facets of cancer research, mouse model research, and relevant technologies. The program is also open to NCI-funded investigators whose research involves investigations of mouse models and who require supplemental support to take advantage of new opportunities afforded by these cancer models.



 

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