Area of research
Oncology · Molecular Biology
Research interest
Dr. Tyler Jacks is a world leader in the field of cancer genetics and is known for his ground-breaking work on the development of genetically-engineered mouse models of cancer (GEMMs). Over the course of his academic career, he has published over 200 peer- reviewed papers along with numerous review articles and book chapters. Dr. Jacks graduated magna cum laude with a BA in Biology in 1983 from Harvard College before becoming a graduate student in the laboratory of Dr. Harold Varmus at the University of California, San Francisco, where he showed that ribosomal frameshifting during translation gives rise to the gag-pol protein of the Rous sarcoma virus, HIV-1 virus and mouse mammary tumor virus. He went on to demonstrate that a stem-loop structure and RNA sequence making up the frameshift site are required for efficient frameshifting in vitro. In 1998, Dr. Jacks returned to Cambridge, Massachusetts, to join Dr. Robert Weinberg’s group as a post-doctoral fellow at the Whitehead Institute, where he developed several GEMMs, including the Rb, p53 and Nf1 mice. In 1992, Dr. Jacks became an assistant professor in the MIT Department of Biology and a member of the MIT Center for Cancer Research, which became the Koch Institute for Integrative Cancer Research at MIT in 2011. In 1994, he became an Assistant Investigator at the Howard Hughes Medical Institute and was promoted to Investigator in 2002. In 2001, Dr. Jacks became Director of the MIT Center for Cancer Research, later the Koch Institute for Integrative Cancer Research at MIT, and recently stepped down as Director after leading the Koch Institute for 20 years. He also resigned as a Howard Hughes Medical Institute Investigator in order to take the role of President at Break Through Cancer. Currently, Dr. Jacks is the David H. Koch Professor of Biology at MIT.
Murine osteosarcoma recapitulates the driver landscape and genomic complexity of osteosarcoma evolution in humans
Pancreatic cancer–restricted cryptic antigens are targets for T cell recognition
Intrinsic electrical activity drives small-cell lung cancer progression
Pancreatic cancer-restricted cryptic antigens are targets for T cell recognition.
Intrinsic electrical activity drives small-cell lung cancer progression.
Lineage identity governs oncogene dependence in murine NSCLC models of KRAS inhibitor resistance
Malignant cell MHC-II immunopeptidomes reveal the evolution of tumor-host interactions
MHC-II antigen presentation on cancer cells improves CD4+ T cell immunity and vaccine efficacy
Deciphering cell states and genealogies of human haematopoiesis
Deciphering cell states and genealogies of human haematopoiesis.
SOX17 enables immune evasion of early colorectal adenomas and cancers
SOX17 enables immune evasion of early colorectal adenomas and cancers.
Spatially resolved analysis of pancreatic cancer identifies therapy-associated remodeling of the tumor microenvironment
Spatially resolved analysis of pancreatic cancer identifies therapy-associated remodeling of the tumor microenvironment
A prime editor mouse to model a broad spectrum of somatic mutations in vivo.
Inhalable point-of-care urinary diagnostic platform
Inhalable point-of-care urinary diagnostic platform.
Longitudinal Intravascular Antibody Labeling Identified Regulatory T Cell Recruitment as a Therapeutic Target in a Mouse Model of Lung Cancer.
Radical Collaboration: Reimagining Cancer Team Science.
The CLCF1-CNTFR axis drives an immunosuppressive tumor microenvironment and blockade enhances the effects of established cancer therapies
Author Correction: Combined inhibition of BET family proteins and histone deacetylases as a potential epigenetics-based therapy for pancreatic ductal adenocarcinoma
Editorial Expression of Concern: p63 and p73 are required for p53-dependent apoptosis in response to DNA damage
Lung adenocarcinoma promotion by air pollutants
Lung adenocarcinoma promotion by air pollutants.
Mismatch repair deficiency is not sufficient to elicit tumor immunogenicity
Mismatch repair deficiency is not sufficient to elicit tumor immunogenicity.
Lymphocyte networks are dynamic cellular communities in the immunoregulatory landscape of lung adenocarcinoma
A prime editor mouse to model a broad spectrum of somatic mutations in vivo
Single-nucleus and spatial transcriptome profiling of pancreatic cancer identifies multicellular dynamics associated with neoadjuvant treatment
Single-nucleus and spatial transcriptome profiling of pancreatic cancer identifies multicellular dynamics associated with neoadjuvant treatment