The molecular genetics component of Program 1 will build on the progress of this aspect of the Program over the past five years. For example, super-enhancers particularly those that appear to control many activated oncogenes, offer possible new approaches to the diagnosis and treatment of cancer. Large non-coding RNAs control gene expression is a focus of research in this Program, and these are likely to control important aspects of tumor genesis. CRISPR technology is a very powerful tool for research on cancer, allowing rapid mutation of many genes in parallel and physically targeting transcription-modulating signals to specific sites on the genome. Small non-coding RNAs such as microRNAs are tightly integrated into networks that control the malignant state, but this has neither been fully illuminated nor set into the regulatory networks of genes important in cancer. These topics and others are developed in the research sections of 1) roles of transcriptional super-enhancers in control of cell identity and cancer, 2) large noncoding RNAs and cancer, 3) probing cancer genomes with CRISPR technology, 4) small non-coding RNAs and cancer, 5) cancer genome and transcriptome analysis, and 6) synthetic biology and cancer. The immunology component of Program 1 features a deep integration of engineering approaches with immunological science to advance our understanding of the interaction of cancer cells with the immune system and develop new forms of immunotherapy. The immunoengineering perspective is a particular strength of the Program and is an instantiation of the broader phenomenon of convergence between engineering and the life sciences in the Koch Institute. Immunology, in particular, is a field that is amenable to both analytical engineering and design engineering. Decoding communications between cells in the immune system using principles of chemical engineering and synthesis and engineering synthetic vaccines using cues from natural immunity are strengths of the Program. These topics and others are discussed in sections 1) therapeutic cancer vaccine development, 2) synergistic antibody/IL-2 immunotherapy, 3) mouse/human models of follicular B cell lymphoma, 4) whole exome sequencing of CTCs as a window into metastatic cancer. Program 1 has 16 Members from 5 Academic Departments at the School of Science or School of Engineering at MIT. The Membership has a cancer-related funding base of $ 24,934,945 TDC. From 4/1/2009, the Membership of Program 1 published 508 cancer-related articles. Of those, 107, or 21%, have involved multiple members; 45, or 8.9%, intra-programmatic, and, 62 or 12.2%, inter-programmatic; 4 are both intra- and interprogrammatic.

Public Health Relevance

Overall Component: Project Narrative The Koch Institute for Integrative Cancer Research at MIT is a highly inter-disciplinary Cancer Center that brings together the great strengths at MIT in cancer science and cancer-oriented engineering to address long- standing problems in the diagnosis and treatment of cancer. The Koch Institute is focused on basic discovery and technology development; however, advancing projects toward the clinic and to the benefit of patients as rapidly as possible is a high priority. This occurs through extensive interactions with clinical centers as well as industry partners.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014051-48
Application #
9693603
Study Section
Subcommittee I - Transistion to Independence (NCI)
Program Officer
Shafik, Hasnaa
Project Start
1997-06-17
Project End
2020-04-30
Budget Start
2019-05-01
Budget End
2020-04-30
Support Year
48
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Miscellaneous
Type
Organized Research Units
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Huang, Hsin-Ho; Qian, Yili; Del Vecchio, Domitilla (2018) A quasi-integral controller for adaptation of genetic modules to variable ribosome demand. Nat Commun 9:5415
GuimarĂ£es, Pedro P G; Gaglione, Stephanie; Sewastianik, Tomasz et al. (2018) Nanoparticles for Immune Cytokine TRAIL-Based Cancer Therapy. ACS Nano 12:912-931
Nath, Samir R; Yu, Zhigang; Gipson, Theresa A et al. (2018) Androgen receptor polyglutamine expansion drives age-dependent quality control defects and muscle dysfunction. J Clin Invest 128:3630-3641
Moynihan, Kelly D; Holden, Rebecca L; Mehta, Naveen K et al. (2018) Enhancement of Peptide Vaccine Immunogenicity by Increasing Lymphatic Drainage and Boosting Serum Stability. Cancer Immunol Res 6:1025-1038
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
Kimmerling, Robert J; Prakadan, Sanjay M; Gupta, Alejandro J et al. (2018) Linking single-cell measurements of mass, growth rate, and gene expression. Genome Biol 19:207
Tang, Li; Zheng, Yiran; Melo, Mariane Bandeira et al. (2018) Enhancing T cell therapy through TCR-signaling-responsive nanoparticle drug delivery. Nat Biotechnol 36:707-716
Holec, Patrick V; Berleant, Joseph; Bathe, Mark et al. (2018) A Bayesian framework for high-throughput T cell receptor pairing. Bioinformatics :
Wong, Madeline Y; Doan, Ngoc Duc; DiChiara, Andrew S et al. (2018) A High-Throughput Assay for Collagen Secretion Suggests an Unanticipated Role for Hsp90 in Collagen Production. Biochemistry 57:2814-2827
Danai, Laura V; Babic, Ana; Rosenthal, Michael H et al. (2018) Altered exocrine function can drive adipose wasting in early pancreatic cancer. Nature 558:600-604

Showing the most recent 10 out of 904 publications