The broad, long-term objective of the project is to provide a solid foundation of knowledge about the cellular biology of cancer and aging. The first part of the project involves a critical analysis of the relationship between the limited lifespan of cells in culture and the long term replication of cells in the organism, particularly of the stem cells. This analysis will encompass the role of telomerase and telomeres in limiting the lifespan of human cells in culture and the relevance of these components to cell survival, differentiation and cancer in the organism. It will include consideration of the safety of the proposed use of artificially immortalized cells for therapy in humans. The second part of the project will compare the genetic stability of cells in culture, in the organism and in cancer. The role of tissue architecture in maintaining homeostasis in the organism will be extensively reviewed. The weakening of this top-down control with age will be considered in the origin of various chronic diseases associated with the aging process. The method is to use close, intensive reading of both the primary historical and the contemporary scientific literature relevant to the subjects. Emphasis will be placed on integrating the biological foundation of each field, often assumed but only superficially understood, with recent molecular findings to develop a more comprehensive, theoretical foundation of cellular change in cancer and aging. Several extensive reviews will be published m leading scientific journals to be followed eventually by unification into a monograph. Amalgamation of these and related subjects in a comprehensive volume is contemplated.

Agency
National Institute of Health (NIH)
Institute
National Library of Medicine (NLM)
Type
Health Sciences Publication Support Awards (NLM) (G13)
Project #
5G13LM007483-02
Application #
6624381
Study Section
Special Emphasis Panel (ZLM1-MMR-M (M3))
Program Officer
Sim, Hua-Chuan
Project Start
2002-05-15
Project End
2005-05-14
Budget Start
2003-05-15
Budget End
2004-05-14
Support Year
2
Fiscal Year
2003
Total Cost
$56,164
Indirect Cost
Name
University of California Berkeley
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Rubin, Harry (2007) Ordered heterogeneity and its decline in cancer and aging. Adv Cancer Res 98:117-47
Rubin, Harry (2007) The logic of the Membrane, Magnesium, Mitosis (MMM) model for the regulation of animal cell proliferation. Arch Biochem Biophys 458:16-23
Rubin, Harry (2006) What keeps cells in tissues behaving normally in the face of myriad mutations? Bioessays 28:515-24
Rubin, Harry (2005) Degrees and kinds of selection in spontaneous neoplastic transformation: an operational analysis. Proc Natl Acad Sci U S A 102:9276-81
Rubin, Harry (2005) Membrane stabilization by intimate contact between cells reduces their Mg2+ activity and suppresses the neoplastic phenotype. Semin Cancer Biol 15:121-31
Rubin, Harry (2005) Magnesium: The missing element in molecular views of cell proliferation control. Bioessays 27:311-20
Rubin, H (2005) Walter Elsasser, prophet of biological complexity, seeker of simplifying rules. Cell Mol Biol (Noisy-le-grand) 51:599-606
Vidair, Charles; Rubin, Harry (2005) Mg2+ as activator of uridine phosphorylation in coordination with other cellular responses to growth factors. Proc Natl Acad Sci U S A 102:662-6
Rubin, Harry (2005) Central roles of Mg2+ and MgATP2- in the regulation of protein synthesis and cell proliferation: significance for neoplastic transformation. Adv Cancer Res 93:1-58
Rubin, Harry (2005) Systemic effects of cancer: role of multiple proteases and their toxic peptide products. Med Sci Monit 11:RA221-8

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