The Biology of Colon Cancer is program remains focused on fundamental cellular and molecular mechanisms of intestinal cell maturation and lineage specific differentiation, and how this establishes and maintains homeostasis of the intestinal mucosa;genetic and environmental factors, and their interactions, that perturb these processes and alter probability of tumor formation and progression;and approaches to prevent tumorigenesis and treat intestinal cancer. Members utilize novel cell systems in culture, mouse genetic models, and human tissues and subjects in their investigations. All of the members are independently funded by grants that are highly cancer focused, and most participate in large multidisciplinary programs that are jointly funded. During the last funding period, this included an NCI U01 Director's Challenge grant on molecular markers of relative drug sensitivity in colon cancer, and subsequently an NCI U54 Center grant on nutritional-genetic interactions in intestinal cancer. This joint funding, and a large number of joint publications, reflects the extensive interactions and collaborations among members of the Program. Moreover, members of the Program collaborate widely across the AECC and have made unique resources available to other Center members. The Program has continued to grow during the last 5 years, both by promotion from within and recruitment, made possible by support from the AECC and a pilot project program funded by the U54 Center grant. Leonard Augenlicht remains the Leader of this Program. There are currently 12 program members from 8 departments, of whom 11 are primary members, supported by 15 NCI ($3.7M Direct) and 2 other NIH grants. Five members are new to the program. Since the last CCSG review there have been 105 cancer-relevant research papers by members of this program of which 34% represent intraprogrammatic, and 33% represent interprogrammatic publications.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013330-37
Application #
7886699
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
37
Fiscal Year
2009
Total Cost
$18,671
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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