Gregory David

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Gregory David

Associate Professor, Department of Biochemistry and Molecular Pharmacology
Biochemistry and Molecular Pharmacology

Contact Info

Address
550 First Avenue
New York, NY 10016

212/263-2926
Gregory.David@nyumc.org

Research Summary

The research interests of our laboratory center on chromatin modifications and its impact on regulation of gene expression and nuclear structure, particularly as it relates changes associated with malignant transformation. Clearly, the interplay between activation and repression of transcription that imposes normal transcriptional control becomes disrupted in cancer. Besides their roles in promoter-specific transcriptional regulation, histone modifiers also play a role in the establishment of large chromosomal domains, and therefore function in maintenance of chromosomal integrity. We and others have shown that deregulation of histone modifying complexes, including Histone Deacetylases (HDACs)-containing complexes, participate to the oncogenic transformation in numerous human cancers. Several studies suggested that blocking the enzymatic activity of HDAC complexes (e.g., using histone deacetylase inhibitors) could prevent tumorigenesis and selectively induce cell death in transformed cells. While HDACs are integral components of several gene regulatory complexes, HDAC inhibitors developed to date exhibit little or no specificity towards individual HDAC-containing complex. Thus, the identification of pathways involved in the modulation of the activities of specific HDAC complexes is a priority in cancer therapy. Knowledge of these control mechanisms in both normal physiology and malignancy is essential for the better understanding of the malignant process that will allow development of novel therapeutic and diagnostic approaches to human disease.
We have recently developed valuable biological tools to study the prominent HDAC-containing complex in mammalian cells, the mSin3-HDAC complex. The mSin3 complex was the first chromatin modifying complex shown to be deregulated in human cancers. However, the molecular basis for the malignant phenotype in those tumors remain unclear, impairing the development of efficient targeted therapies. Using genetic recombination, we generated mouse strains that can be spatially and temporally genetically inactivated for different components of the mSin3-HDAC complex. Those unique reagents will enable the precise delineation of the in vivo consequences of deregulation or inactivation of the complex on mammalian development and oncogenesis, and enable the development of rational targeted therapies.

Research Interests

Chromatin modifications in development and oncogenesis

Structural insights into the assembly of the histone deacetylase-associated Sin3L/Rpd3L corepressor complex
Clark, Michael D; Marcum, Ryan; Graveline, Richard; Chan, Clarence W; Xie, Tao; Chen, Zhonglei; Ding, Yujia; Zhang, Yongbo; Mondragon, Alfonso; David, Gregory; Radhakrishnan, Ishwar
2015-07-05; 1091-6490,Proceedings of the National Academy of Sciences of the United States of America (PNAS) - id: 1649842, year: 2015 JOURNAL ARTICLE

Transcriptional repression of Sin3B by Bmi-1 prevents cellular senescence and is relieved by oncogene activation
DiMauro, T; Cantor, D J; Bainor, A J; David, G
2015-07-26; 1476-5594,Oncogene - id: 1684282, year: 2015 Journal Article

Senescence-associated SIN3B promotes inflammation and pancreatic cancer progression
Rielland, Maite; Cantor, David J; Graveline, Richard; Hajdu, Cristina; Mara, Lisa; Diaz, Beatriz de Diego; Miller, George; David, Gregory
2014-07-07; 0021-9738,Journal of clinical investigation - id: 1061672, year: 2014 Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

The senescence-associated Sin3B protein promotes inflammation and pancreatic cancer progression
Rielland, Maite; Cantor, David; Graveline, Richard; Hadju, Cristina; Mara, Lisa; Miller, George; David, Gregory
2015-05-28; 1538-7445,Cancer research - id: 1599342, year: 2014

Inhibition of androgen receptor and ?-catenin activity in prostate cancer
Lee, E; Madar, A; David, G; Garabedian, MJ; Gupta, RD; Logan, SK
2014-02-04; 0027-8424,Proceedings of the National Academy of Sciences of the United States of America (PNAS) - id: 785132, year: 2013