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
Evensen, Nikki A; Madhusoodhan, P Pallavi; Meyer, Julia et al. (2018) MSH6 haploinsufficiency at relapse contributes to the development of thiopurine resistance in pediatric B-lymphoblastic leukemia. Haematologica 103:830-839
Lee, Hyun-Wook; Park, Sung-Hyun; Weng, Mao-Wen et al. (2018) E-cigarette smoke damages DNA and reduces repair activity in mouse lung, heart, and bladder as well as in human lung and bladder cells. Proc Natl Acad Sci U S A 115:E1560-E1569
Sun, Qi; Rabbani, Piul; Takeo, Makoto et al. (2018) Dissecting Wnt Signaling for Melanocyte Regulation during Wound Healing. J Invest Dermatol 138:1591-1600
Formenti, Silvia C; Rudqvist, Nils-Petter; Golden, Encouse et al. (2018) Radiotherapy induces responses of lung cancer to CTLA-4 blockade. Nat Med 24:1845-1851
Xu, Yang; Taylor, Paul; Andrade, Joshua et al. (2018) Pathologic Oxidation of PTPN12 Underlies ABL1 Phosphorylation in Hereditary Leiomyomatosis and Renal Cell Carcinoma. Cancer Res 78:6539-6548
Gagner, Jean-Pierre; Zagzag, David (2018) Probing Glioblastoma Tissue Heterogeneity with Laser Capture Microdissection. Methods Mol Biol 1741:209-220
Tsay, Jun-Chieh J; Wu, Benjamin G; Badri, Michelle H et al. (2018) Airway Microbiota Is Associated with Upregulation of the PI3K Pathway in Lung Cancer. Am J Respir Crit Care Med 198:1188-1198
Martin, Patricia K; Marchiando, Amanda; Xu, Ruliang et al. (2018) Autophagy proteins suppress protective type I interferon signalling in response to the murine gut microbiota. Nat Microbiol 3:1131-1141
de la Parra, Columba; Ernlund, Amanda; Alard, Amandine et al. (2018) A widespread alternate form of cap-dependent mRNA translation initiation. Nat Commun 9:3068
Coux, RĂ©mi-Xavier; Teixeira, Felipe Karam; Lehmann, Ruth (2018) L(3)mbt and the LINT complex safeguard cellular identity in the Drosophila ovary. Development 145:

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