The overall objective of the Environmental Epigenetics and Molecular Analyses Facility Core (EEMAFC) is to provide Center members with access to, and education on using, state-of-the-art tools for assessing the effects of environment exposures on the epigenomes and genomes of cells, tissues and organs of humans and other species. It has become increasingly evident that the epigenome plays an enormous role in modulating the responses of organisms to myriad environmental exposures. Thus, new initiatives that have been implemented since the last renewal include the now routinely used RNA-Seq and ChIP-Seq for transcriptome and chromatin status discovery for investigating mechanisms underlying toxic and disease responses to environmental agents. In addition to the expanded epigenetics services, the Core also continues to provide basic molecular, microscopy and analytical services in support of ongoing epigenetics, genomics, gene expression, and signaling pathway research in the Center. These include basic molecular and analytical services, including new equipment for high throughput qPCR, for example, and new equipment for metals analysis in cells and tissues of exposed organisms, since metal effects on the epigenome, genome and cell functions are specialized research strengths of the NYU NIEHS Center. The rationale for the continuing evolution of this Core reflects current trends in environmental health research, in particular the rapidly changing field investigating environment interactions on epigenomes/genomes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES000260-54
Application #
9491808
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
54
Fiscal Year
2018
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Wang, Sophia S; Carrington, Mary; Berndt, Sonja I et al. (2018) HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes. Cancer Res 78:4086-4096
Church, Jamie S; Tijerina, Pamella B; Emerson, Felicity J et al. (2018) Perinatal exposure to concentrated ambient particulates results in autism-like behavioral deficits in adult mice. Neurotoxicology 65:231-240
Jin, Honglei; Sun, Wenrui; Zhang, Yuanmei et al. (2018) MicroRNA-411 Downregulation Enhances Tumor Growth by Upregulating MLLT11 Expression in Human Bladder Cancer. Mol Ther Nucleic Acids 11:312-322
Chen, Danqi; Fang, Lei; Li, Hongjie et al. (2018) The effects of acetaldehyde exposure on histone modifications and chromatin structure in human lung bronchial epithelial cells. Environ Mol Mutagen 59:375-385
Hua, Xiaohui; Xu, Jiheng; Deng, Xu et al. (2018) New compound ChlA-F induces autophagy-dependent anti-cancer effect via upregulating Sestrin-2 in human bladder cancer. Cancer Lett 436:38-51
Choi, Byeong Hyeok; Philips, Mark R; Chen, Yuan et al. (2018) K-Ras Lys-42 is crucial for its signaling, cell migration, and invasion. J Biol Chem 293:17574-17581
Peng, Minggang; Wang, Jingjing; Zhang, Dongyun et al. (2018) PHLPP2 stabilization by p27 mediates its inhibition of bladder cancer invasion by promoting autophagic degradation of MMP2 protein. Oncogene :
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
Choi, Byeong Hyeok; Chen, Changyan; Philips, Mark et al. (2018) RAS GTPases are modified by SUMOylation. Oncotarget 9:4440-4450
Li, Xin; Tian, Zhongxian; Jin, Honglei et al. (2018) Decreased c-Myc mRNA Stability via the MicroRNA 141-3p/AUF1 Axis Is Crucial for p63? Inhibition of Cyclin D1 Gene Transcription and Bladder Cancer Cell Tumorigenicity. Mol Cell Biol 38:

Showing the most recent 10 out of 407 publications