The program in Environmental and Molecular Carcinogenesis integrates investigators from several different departments on 4 distinct NYU campuses: Sterling Forest (14), the School of Medicine (24), Dental School (3) and Washington Square (2) sharing a common interest in understanding the Environmental causes of cancer. The overall goal of the program is to understand the environmental etiology of cancer and to use this information for cancer prevention and early detection. This research program focuses on: (1)The mechanisms of action by environmental carcinogens by investigating their effects on the structure and function of cellular macromolecules. Macromolecules of interest include DNA and proteins, particularly those involved with signaling, transcription control, and susceptibility to environmental agents. These studies are carried out in humans, as well as in vivo and in vitro models. (2) Inorganic compounds, such as arsenic, nickel, chromium, and iron. The molecular toxicological effects of metals and other agents are studied by examining their interactions with DNA and with proteins, which have structural, regulatory or enzymatic activities. (3) The formation of reactive oxygen species, their biochemistry, and the biological effects that might result from their actions. (4) The mutational specificity of carcinogens and site-specific mutagenesis of particular DNA lesions, the molecular basis for genetic susceptibility to environmental agents, the effects of hormones on gene expression and carcinogenesis, and chemoprevention. (5) Epigenetic mechanisms of carcinogenesis. (6) Antioxidants and the prevention of tumor formation as well as developing biomarkers for early detection of cancer. (7) Epidemiology and molecular epidemiology approaches to cancer etiology. Research in this program is divided thematically into five groups: 1) DNA adducts, DNA Damage and Repair; 2) Carcinogenesis and Animal Models;3) Chemoprevention;4) Cell Signaling and Epigenetic Mechanisms of Carcinogenesis;and 5) Early Detection and Cancer Epidemiology.Dr Costa is the Director of the Program. ? Total funding increased from $7,668,974 to $22,551,198. Membership has increased from 21 to 47. Total publications include 627 of which 12% are intra-programmatic and 8% are inter-programmatie.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016087-32
Application #
8376772
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
2013-02-28
Budget Start
2012-03-01
Budget End
2013-02-28
Support Year
32
Fiscal Year
2012
Total Cost
$27,944
Indirect Cost
$13,399
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Chiou, Kenneth L; Bergey, Christina M (2018) Methylation-based enrichment facilitates low-cost, noninvasive genomic scale sequencing of populations from feces. Sci Rep 8:1975
Pelzek, Adam J; Shopsin, Bo; Radke, Emily E et al. (2018) Human Memory B Cells Targeting Staphylococcus aureus Exotoxins Are Prevalent with Skin and Soft Tissue Infection. MBio 9:
Kourtis, Nikos; Lazaris, Charalampos; Hockemeyer, Kathryn et al. (2018) Oncogenic hijacking of the stress response machinery in T cell acute lymphoblastic leukemia. Nat Med 24:1157-1166
Jose, Cynthia C; Jagannathan, Lakshmanan; Tanwar, Vinay S et al. (2018) Nickel exposure induces persistent mesenchymal phenotype in human lung epithelial cells through epigenetic activation of ZEB1. Mol Carcinog 57:794-806
Snuderl, Matija; Kannan, Kasthuri; Pfaff, Elke et al. (2018) Recurrent homozygous deletion of DROSHA and microduplication of PDE4DIP in pineoblastoma. Nat Commun 9:2868
Formenti, Silvia C; Lee, Percy; Adams, Sylvia et al. (2018) Focal Irradiation and Systemic TGF? Blockade in Metastatic Breast Cancer. Clin Cancer Res 24:2493-2504
Lee, Chul-Hwan; Yu, Jia-Ray; Kumar, Sunil et al. (2018) Allosteric Activation Dictates PRC2 Activity Independent of Its Recruitment to Chromatin. Mol Cell 70:422-434.e6
Stafford, James M; Lee, Chul-Hwan; Voigt, Philipp et al. (2018) Multiple modes of PRC2 inhibition elicit global chromatin alterations in H3K27M pediatric glioma. Sci Adv 4:eaau5935
Jung, Heekyung; Baek, Myungin; D'Elia, Kristen P et al. (2018) The Ancient Origins of Neural Substrates for Land Walking. Cell 172:667-682.e15
Aiello, Nicole M; Maddipati, Ravikanth; Norgard, Robert J et al. (2018) EMT Subtype Influences Epithelial Plasticity and Mode of Cell Migration. Dev Cell 45:681-695.e4

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