The Center for Cancer Research (CCR) at MIT was established twenty years ago to conduct basic research in areas relevant to cancer. The CCR is an autonomous administrative unit with its own assigned space (53,343 sq. ft) and faculty slots under the control of the CCR Director, who reports to the Dean of Science. The CCR currently has 13 Staff Investigators and 6 Affiliate Investigators. The CCR has a total staff of 170-180 researchers and the Affiliate labs represent more than 100 additional people. The CCR has its own administrative office responsible for management of the CCSG and research grants of the CCR, and of shared research facilities which include Biopolymers, Cell Sorter, Glassware, Media Preparation, Quantitation & Computing, Research Microscopy & Photography, and Transgenic Animal & Histology facilities. The established research programs in the CCR are Molecular Genetics, Cell & Developmental Biology, and Immunology and the strengths of the CCR research lie in basic cell and molecular biology and, in recent years, the application of transgenic mouse methods the generate animal models of cancer and other diseases. Areas of emphasis include the discovery and analyses of oncogenes and tumor suppressor genes and other disease genes, regulation of gene transcription and RNA splicing, cell adhesion in normal and pathological situations, structure and function of the cytoskeleton, processing of cell surface proteins, antigen processing and presentation, and T & B cell development. In addition to its strengths in basic research, the CCR performs an important role in training future researchers in biomedical science, including undergraduate and graduate students, postdoctoral and clinical fellows. Extensive collaborations exist with medical schools, hospitals and the biotechnology/pharmaceutical industries. Thus, the research in the CCR has a major impact both on the fundamental understanding of cancer and on translation to and from the clinical arena.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014051-28
Application #
2894451
Study Section
Cancer Centers and Research Programs Review Committee (CCRP)
Program Officer
Shafik, Hasnaa
Project Start
1975-09-01
Project End
2000-04-30
Budget Start
1999-07-08
Budget End
2000-04-30
Support Year
28
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
Organized Research Units
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Lannagan, Tamsin R M; Lee, Young K; Wang, Tongtong et al. (2018) Genetic editing of colonic organoids provides a molecularly distinct and orthotopic preclinical model of serrated carcinogenesis. Gut :
Filbin, Mariella G; Tirosh, Itay; Hovestadt, Volker et al. (2018) Developmental and oncogenic programs in H3K27M gliomas dissected by single-cell RNA-seq. Science 360:331-335
Roper, Jatin; Tammela, Tuomas; Akkad, Adam et al. (2018) Colonoscopy-based colorectal cancer modeling in mice with CRISPR-Cas9 genome editing and organoid transplantation. Nat Protoc 13:217-234
Suzuki, Hiroshi I; Spengler, Ryan M; Grigelioniene, Giedre et al. (2018) Deconvolution of seed and RNA-binding protein crosstalk in RNAi-based functional genomics. Nat Genet 50:657-661
McKenney, Anna Sophia; Lau, Allison N; Somasundara, Amritha Varshini Hanasoge et al. (2018) JAK2/IDH-mutant-driven myeloproliferative neoplasm is sensitive to combined targeted inhibition. J Clin Invest 128:789-804
Richardson, Christopher E R; Cunden, Lisa S; Butty, Vincent L et al. (2018) A Method for Selective Depletion of Zn(II) Ions from Complex Biological Media and Evaluation of Cellular Consequences of Zn(II) Deficiency. J Am Chem Soc 140:2413-2416
Choudhury, Atish D; Werner, Lillian; Francini, Edoardo et al. (2018) Tumor fraction in cell-free DNA as a biomarker in prostate cancer. JCI Insight 3:
Chen, Pan-Yu; Muzumdar, Mandar Deepak; Dorans, Kimberly Judith et al. (2018) Adaptive and Reversible Resistance to Kras Inhibition in Pancreatic Cancer Cells. Cancer Res 78:985-1002
Wong, Madeline Y; Chen, Kenny; Antonopoulos, Aristotelis et al. (2018) XBP1s activation can globally remodel N-glycan structure distribution patterns. Proc Natl Acad Sci U S A 115:E10089-E10098
Viswanathan, Srinivas R; Nogueira, Marina F; Buss, Colin G et al. (2018) Genome-scale analysis identifies paralog lethality as a vulnerability of chromosome 1p loss in cancer. Nat Genet 50:937-943

Showing the most recent 10 out of 904 publications