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Cell and Molecular Biology Graduate Group


Brian Keith
Associate Investigator and Director of Education, Abramson Family Cancer Research Institute
Adjunct Associate Professor, Department of Cancer Biology
Chair, Cancer Biology Program, CAMB

Cancer Biology Program


Address

453 Biomedical Rsch Bldg (BRB) II/III
421 Curie Boulevard
Philadelphia, PA 19104-6140

Office tel.: 215 746-5533
Lab tel.: 215 746-5526
Fax: 215 746-5511

E-mail: bkeith@mail.med.upenn.edu


Link(s)

Dr. Celeste Simon's Lab Page

EDUCATION

Brown University: BS (Biology), 1980.

Rockefeller University: PhD (Plant Molecular Biology), 1987.

RESEARCH INTERESTS

  • How cells and tissues adapt to oxygen deprivation (hypoxia) by modifying gene expression..
  • Key words:

  • mouse, development, transcription, hypoxia, cancer.
  • PubMed Search
    Search PubMed for articles

    DESCRIPTION OF RESEARCH

    As part of a long-standing collaboration with Dr. Celeste Simon, I generate mouse models in which genes encoding critical components of the hypoxic response pathway are mutated. These tools offer insights into physiological responses to hypoxia during normal development, as well as in pathological contexts (ischemia, cancer).

    RECENT PUBLICATIONS

    Keith, B., and Simon, M. C. (2007) Hypoxia Inducible Factors, stem cells, and cancer. Cell. 129: 465-472.

    Gruber, M., Hu, C.-J., Johnson, R. D., Brown, E. J., Keith, B., and Simon, M. C. (2007) Acute postnatal ablation of Hif-2α results in anemia. Proc. Natl. Acad. Sci. 104: 2301-2306.

    Covello, K.L., Kehler, J., Yu, H., Gordan, J.G., Arsham, A.M., Hu, C.-J., Labosky, P.A., Simon, M.C., and Keith, B. (2006) HIF-2± regulates Oct-4: effects of hypoxia on stem cell function, embryonic development, and tumor growth. Genes & Dev. 20: 557-570.

    Liu, L., Cash, T.P., Jones, R.G., Keith, B., Thompson, C.B., and Simon, M.C. (2006) Hypoxia induced energy stress regulates mRNA translation and cell growth. Molecular Cell 21: 521-531.

    Covello, K.L., Simon, M.C., and Keith, B. (2005) Targeted replacement of HIF-1α by a HIF-2α knock-in allele promotes tumor growth. Cancer Research 65: 2277-2286.

    Mansfield, K.D., M.C. Simon, and B. Keith. (2004). Hypoxic reduction of intracellular gluathione requires mitochondrial reactive oxygen species (mtROS). J. Applied Physiol. 97(4):1358-66.

    Brunelle, J.K., M.T. Santore, G. R. Budinger, Y. Tang, T.A. Barrett, W.X. Zong, E. Kandel, B. Keith, M.C. Simon, C.B. Thompson, N. Hay, and N.S. Chandel. (2003). c-Myc sensitization to oxygen deprivation induced cell death is dependent on Bax/Bak but independent of p53 and HIF-1. J. Biol. Chem. 279:4305-12.

    Mack, F., W. K. Rathmell, A. Arsham, J. Gnarra, B. Keith, and M. C. Simon. (2003) Loss of pVHL is sufficient to cause HIF dysregulation in primary cells but does not promote tumor growth. Cancer Cell 3: 75-88.

    Hu, C.-J., L.Y. Wang,, L. A. Chodosh, B. Keith, and M.C. Simon. (2003). Differential Roles of HIF-1α and HIF-2α in hypoxic gene regulation. Mol. Cell. Biol. 23:9361-74.

    Lab

    Rotation Projects

    Students intersted in rotation projects should refer to Dr. Celeste Simon's lab page.

    Lab personnel:
    Please refer to Dr. Celeste Simon's lab.
     
    last updated 10/2007
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