Research by members of the Cell Growth and Differentiation Control Program is focused on identifying andunderstanding the mechanisms of action of the cellular factors that control proliferation, differentiation andcell death, how the programs controlling these processes are coordinated and how they interact. The majorscientific goals are: (1) to identify, characterize and study the mechanisms of action of gene productscontrolling cell proliferation, lineage commitment and cell differentiation, and cell death; (2) to understandhow misregulation of these gene products and processes contribute to oncogenesis; (3) to use thisknowledge to develop new approaches to cancer prevention and treatment. A major scientific focus of theprogram is the control of gene expression during the cell cycle, differentiation and apoptosis and the key roleplayed by transcription factors in regulating these processes. Many members of the program are alsostudying the role of epigenetic mechanisms in cancer, including changes in the patterns of histonemodifications and DMA methylation in cancer cells. A new method for genome-wide methylation analyseshas been developed by a program member for these studies and, along with a highly versatile arrayplatform, is being used to study gene expression and epigenetic changes during normal cell growth anddifferentiation in a variety of malignancies and premalignant conditions. Within the program there areparticular strengths in studying the properties of stem cells, both adult stem cells and human embryonic stemcells, as well as in three organ systems: the hematopoietic system, the liver, and neuronal cells. Theprogram has benefited from members whose research programs utilize nonmammalian model organismsincluding yeast, Drosophila, and zebrafish. The research of the group's members is also strengthened byinvestigators with expertise in the most advanced approaches for studying control of gene expression ineukaryotic cells. There are currently 26 program members from 10 departments, of whom 25 are primarymembers, supported by 9 NCI ($1.8M Direct) and 33 other NIH grants. There have been 5 new recruits tothis program. Since the last CCSG review there have been 439 cancer-relevant research papers bymembers of this program of which 8% represent intraprogrammatic, and 20% represent interprogrammaticcollaborations.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013330-35
Application #
7506802
Study Section
Subcommittee G - Education (NCI)
Project Start
2007-09-25
Project End
2012-06-30
Budget Start
2007-09-25
Budget End
2008-06-30
Support Year
35
Fiscal Year
2007
Total Cost
$23,414
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Willis, Ian M; Moir, Robyn D; Hernandez, Nouria (2018) Metabolic programming a lean phenotype by deregulation of RNA polymerase III. Proc Natl Acad Sci U S A 115:12182-12187
Hayama, Ryo; Sparks, Samuel; Hecht, Lee M et al. (2018) Thermodynamic characterization of the multivalent interactions underlying rapid and selective translocation through the nuclear pore complex. J Biol Chem 293:4555-4563
Martynova, Elena; Bouchard, Maxime; Musil, Linda S et al. (2018) Identification of Novel Gata3 Distal Enhancers Active in Mouse Embryonic Lens. Dev Dyn 247:1186-1198
Huang, Kezhen; Mukherjee, Subhajit; DesMarais, Vera et al. (2018) Targeting the PXR-TLR4 signaling pathway to reduce intestinal inflammation in an experimental model of necrotizing enterocolitis. Pediatr Res 83:1031-1040
Bines, Jose; Tevaarwerk, Amye J (2018) Baby steps: Pregnancy outcomes after human epidermal growth factor receptor 2-targeted therapy. Cancer :
Mathew, Deepti; Wang, Yanhua; Van Arsdale, Anne et al. (2018) Expression of ?V-Tubulin in Secretory Cells of the Fallopian Tube Epithelium Marks Cellular Atypia. Int J Gynecol Cancer 28:363-370
Mao, Kai; Quipildor, Gabriela Farias; Tabrizian, Tahmineh et al. (2018) Late-life targeting of the IGF-1 receptor improves healthspan and lifespan in female mice. Nat Commun 9:2394
Entenberg, David; Voiculescu, Sonia; Guo, Peng et al. (2018) A permanent window for the murine lung enables high-resolution imaging of cancer metastasis. Nat Methods 15:73-80
Iqbal, Niloy Jafar; Lu, Zhonglei; Liu, Shun Mei et al. (2018) Cyclin-dependent kinase 4 is a preclinical target for diet-induced obesity. JCI Insight 3:
Sharma, Yogeshwar; Liu, Jinghua; Kristian, Kathleen E et al. (2018) In Atp7b-/- Mice Modeling Wilson's Disease Liver Repopulation with Bone Marrowderived Myofibroblasts or Inflammatory Cells and not Hepatocytes is Deleterious. Gene Expr :

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