The overall responsibility for administration of the scientific and technical activities of the Program will be carried out by Dr. Steven R. Tannenbaum. It is planned to conduct periodic reviews of the overall program activities through seminars for the technical staff and meetings of the principal investigators. Reports and scientific papers will be collected in a central office under his direction assisted by Ms. Amy Francis. Since all of the co-project leaders are at MIT, informal meetings are frequent and lead to a natural process of exchange of information and ideas. The Administrative Unit will consist of Professor Tannenbaum, Program Director and Ms. Amy Francis, Administrative Assistant. It will be the responsibility of this Unit to oversee and coordinate progress reports and publications relevant to this grant. Each Project and Core will report on a monthly basis, financial information, publications and progress reports. Monthly financial reports are monitored and maintained by Ms. Francis. She will also communicate with the Administrative Assistant and the Project Leader of each Project or Core to verify financial management information provided by the MIT accounting system. Each Project and Core are responsible for reconciling statements to compare estimated costs with actual expenditures and to ensure proper documentation is maintained. A repository of technical reports, manuscripts and reprints of publications has been established and will be maintained in the office of the Program Director by Ms. Francis. An important function for Core 3 is the coordination of activities with scientific collaborators. These include Elizabeth Grimm at M.D.Anderson Hospital, Curtis Harris of the National Cancer Institute, Stephen Lloyd of the Oregon Health Sciences Center, Kent Sugden of the University of Montana, and Melanie Ihrig of the Methodist Hospital Research Institute. The collaboration with Dr. Grimm relates to the melanoma SPORE, Dr. Harris with diseased colonic tissue, Dr. Lloyd with cells and mice that are repair deficient for hyperoxidized bases, Dr. Sugden with cells treated with metal oxidants, and Dr. Ihrig with statistical analysis of the animal studies. In addition to the formal collaborations, we receive frequent inquiries about methods and requests for analytical services. This includes providing nitrate/nitrite analysis in biological samples, exposure of cells to NO, and mass spectrometry.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA026731-34
Application #
8567219
Study Section
Special Emphasis Panel (ZCA1-GRB-P)
Project Start
Project End
2014-12-31
Budget Start
2013-01-01
Budget End
2013-12-31
Support Year
34
Fiscal Year
2013
Total Cost
$92,739
Indirect Cost
$37,332
Name
Massachusetts Institute of Technology
Department
Type
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Gu, Chen; Ramos, Jillian; Begley, Ulrike et al. (2018) Phosphorylation of human TRM9L integrates multiple stress-signaling pathways for tumor growth suppression. Sci Adv 4:eaas9184
Wadduwage, Dushan N; Kay, Jennifer; Singh, Vijay Raj et al. (2018) Automated fluorescence intensity and gradient analysis enables detection of rare fluorescent mutant cells deep within the tissue of RaDR mice. Sci Rep 8:12108
Tajai, Preechaya; Fedeles, Bogdan I; Suriyo, Tawit et al. (2018) An engineered cell line lacking OGG1 and MUTYH glycosylases implicates the accumulation of genomic 8-oxoguanine as the basis for paraquat mutagenicity. Free Radic Biol Med 116:64-72
Rothenberg, Daniel A; Taliaferro, J Matthew; Huber, Sabrina M et al. (2018) A Proteomics Approach to Profiling the Temporal Translational Response to Stress and Growth. iScience 9:367-381
Wang, Xin; Garcia, Carlos T; Gong, Guanyu et al. (2018) Automated Online Solid-Phase Derivatization for Sensitive Quantification of Endogenous S-Nitrosoglutathione and Rapid Capture of Other Low-Molecular-Mass S-Nitrosothiols. Anal Chem 90:1967-1975
Chan, Cheryl; Pham, Phuong; Dedon, Peter C et al. (2018) Lifestyle modifications: coordinating the tRNA epitranscriptome with codon bias to adapt translation during stress responses. Genome Biol 19:228
Fedeles, Bogdan I (2017) G-quadruplex-forming promoter sequences enable transcriptional activation in response to oxidative stress. Proc Natl Acad Sci U S A 114:2788-2790
Townsend, Todd A; Parrish, Marcus C; Engelward, Bevin P et al. (2017) The development and validation of EpiComet-Chip, a modified high-throughput comet assay for the assessment of DNA methylation status. Environ Mol Mutagen 58:508-521
Kimoto, Takafumi; Kay, Jennifer E; Li, Na et al. (2017) Recombinant cells in the lung increase with age via de novo recombination events and clonal expansion. Environ Mol Mutagen 58:135-145
Edrissi, Bahar; Taghizadeh, Koli; Moeller, Benjamin C et al. (2017) N6-Formyllysine as a Biomarker of Formaldehyde Exposure: Formation and Loss of N6-Formyllysine in Nasal Epithelium in Long-Term, Low-Dose Inhalation Studies in Rats. Chem Res Toxicol 30:1572-1576

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