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Accession Number:
ADA624300
Title:
Understanding and Targeting Epigenetic Alterations in Acquired Bone Marrow Failure
Descriptive Note:
Annual rept. 1 May 2014-30 Apr 2015
Corporate Author:
MEMORIAL SLOAN-KETTERING CANCER CENTER NEW YORK
Report Date:
2015-05-01
Pagination or Media Count:
40.0
Abstract:
Systematic genomic discovery efforts in patients with bone marrow failure due to myelodysplastic syndrome MDS has led to the rapid discovery of recurrent somatic genetic alterations underlying these disorders. Remarkably, a large number of these mutations occur in genes whose function is known, or suspected, to be involved in epigenetic regulation of gene transcription. This includes mutations in ASXL1, TET2, and EZH2. The goals of our proposal were to 1 perform functional genetic characterization of these alterations, 2 determine if these alterations are therapeutically targetable, and 3 perform detailed genomic analysis of specific subsets of MDS patients with no known genetic alterations and with severe bone marrow failure to discover additional genetic alterations contributing to MDS pathogenesis. Since funding of this award we have made major progress in 1 understanding the impact of ASXL1 mutations and loss on chromatin Abdel Wahab, et al. Cancer Cell 2012, 2 identifying the in vivo biological effects of deletion of Asxl1 and Tet2 alone and in combination with one another Abdel- Wahab, et al. J Exp Med 2013, and 3 identified the genome- wide effects of Asxl1 on transcription Abdel- Wahab, et al. J Exp Med 2013 and Abdel- Wahab, O, et al. Leukemia 2013. More recently we have identified that recently common mutations in the splicing machinery in MDS also may impact the function of these epigenetic modifiers Kim, E, et al. Cancer Cell 2015.
Distribution Statement:
APPROVED FOR PUBLIC RELEASE
