P50CA254897
Project Grant
Overview
Grant Description
Epigenetic Therapies - New Approaches - Abstract (Overall)
Epigenetics refers to stable gene expression patterns mediated by DNA methylation and/or chromatin remodeling and is involved in cellular identity and repression of spurious transcription, including from repetitive elements.
Over the past 20 years, in work led in part by investigators in this application, epigenetic changes were recognized as important drivers of cancer formation, progression, and resistance to therapy. This recognition, along with the reversible nature of the biochemical modifications required for epigenetics, led to the field of epigenetic therapy, which aims to reprogram gene expression to achieve a therapeutic effect.
This field, which started with DNA methyltransferase (DNMT) inhibitors, has grown to a dozen epigenetic targets and over 30 drugs in clinical trials. Four targets have made it to US-FDA approval (DNMTs, histone deacetylases (HDACs), EZH2, and isocitrate dehydrogenases), and tens of thousands of cancer patients benefit from this every year.
With the identification of new targets and the recognition that epigenetics is involved in sensitivity and resistance to chemotherapy and immunotherapy, the clinical potential of epigenetic therapy has begun to be explored in earnest. There remain fundamental challenges, from the lack of robust biomarkers of activity, to the emergence of resistance, and to the unexplained divide in responses between hematologic malignancies and solid tumors. This SPORE application will address all of these challenges.
The SPORE team consists of investigators who are pioneers in the fields of cancer epigenetics and epigenetic therapy and explores new epigenetic targets and combination strategies along with a robust biomarker analysis pipeline to identify patients likely to respond and pharmacodynamic markers of response. The team leverages a strong clinical and translational pipeline built through the Van Andel Institute Stand Up to Cancer Epigenetics Dream Team, which has conducted 14 epigenetic therapy clinical trials in the past few years, and is fully committed to the clinical trials proposed in this application.
This epigenetic therapy SPORE encompasses four major themes: (I) develop and test drugs against new epigenetic targets (Projects 1, 2), (II) mechanistic and translational studies of immunosensitization by epigenetic therapy (Projects 1-3), (III) studies of drug combinations that enhance the efficacy of known epigenetic drugs (Projects 1-3), and (IV) biomarker studies to define sensitivity and resistance to epigenetic therapy in the clinic (all projects).
These themes will be addressed through 3 projects: (I) cyclin-dependent kinases as epigenetic therapy targets; (II) epigenetic synergy between DNMT and EZH1/2 inhibitors; (III) linking epigenetic therapy induction of inflammasome signaling to generation of a BRCA-ness phenotype.
These projects will be supported by three cores (administrative, pathology, genomics), and a key goal will also be to mentor the next generation of epigenetic therapy investigators and support cutting-edge science through the career enhancement and developmental research programs.
Epigenetics refers to stable gene expression patterns mediated by DNA methylation and/or chromatin remodeling and is involved in cellular identity and repression of spurious transcription, including from repetitive elements.
Over the past 20 years, in work led in part by investigators in this application, epigenetic changes were recognized as important drivers of cancer formation, progression, and resistance to therapy. This recognition, along with the reversible nature of the biochemical modifications required for epigenetics, led to the field of epigenetic therapy, which aims to reprogram gene expression to achieve a therapeutic effect.
This field, which started with DNA methyltransferase (DNMT) inhibitors, has grown to a dozen epigenetic targets and over 30 drugs in clinical trials. Four targets have made it to US-FDA approval (DNMTs, histone deacetylases (HDACs), EZH2, and isocitrate dehydrogenases), and tens of thousands of cancer patients benefit from this every year.
With the identification of new targets and the recognition that epigenetics is involved in sensitivity and resistance to chemotherapy and immunotherapy, the clinical potential of epigenetic therapy has begun to be explored in earnest. There remain fundamental challenges, from the lack of robust biomarkers of activity, to the emergence of resistance, and to the unexplained divide in responses between hematologic malignancies and solid tumors. This SPORE application will address all of these challenges.
The SPORE team consists of investigators who are pioneers in the fields of cancer epigenetics and epigenetic therapy and explores new epigenetic targets and combination strategies along with a robust biomarker analysis pipeline to identify patients likely to respond and pharmacodynamic markers of response. The team leverages a strong clinical and translational pipeline built through the Van Andel Institute Stand Up to Cancer Epigenetics Dream Team, which has conducted 14 epigenetic therapy clinical trials in the past few years, and is fully committed to the clinical trials proposed in this application.
This epigenetic therapy SPORE encompasses four major themes: (I) develop and test drugs against new epigenetic targets (Projects 1, 2), (II) mechanistic and translational studies of immunosensitization by epigenetic therapy (Projects 1-3), (III) studies of drug combinations that enhance the efficacy of known epigenetic drugs (Projects 1-3), and (IV) biomarker studies to define sensitivity and resistance to epigenetic therapy in the clinic (all projects).
These themes will be addressed through 3 projects: (I) cyclin-dependent kinases as epigenetic therapy targets; (II) epigenetic synergy between DNMT and EZH1/2 inhibitors; (III) linking epigenetic therapy induction of inflammasome signaling to generation of a BRCA-ness phenotype.
These projects will be supported by three cores (administrative, pathology, genomics), and a key goal will also be to mentor the next generation of epigenetic therapy investigators and support cutting-edge science through the career enhancement and developmental research programs.
Funding Goals
TO PROVIDE AN ORGANIZATIONAL FOCUS AND STIMULUS FOR THE HIGHEST QUALITY CANCER RESEARCH THAT EFFECTIVELY PROMOTES INTERDISCIPLINARY CANCER RESEARCH AIMED TOWARD THE ULTIMATE GOAL OF REDUCING CANCER INCIDENCE, MORTALITY AND MORBIDITY. THE CANCER CENTER SUPPORT GRANT (CCSG) PROVIDES THE RESOURCES AND INFRASTRUCTURE TO FACILITATE THE COORDINATION OF INTERDISCIPLINARY PROGRAMS ACROSS A BROAD SPECTRUM OF RESEARCH FROM BASIC LABORATORY RESEARCH TO CLINICAL INVESTIGATION TO POPULATION SCIENCE. THE CCSG SUPPORTS SALARIES FOR SCIENTIFIC LEADERSHIP OF THE CENTER, SHARED RESOURCES FOR FUNDED CENTER INVESTIGATORS, CERTAIN ADMINISTRATIVE COSTS, PLANNING AND EVALUATION, AND DEVELOPMENTAL FUNDS FOR NEW RECRUITMENTS AND FEASIBILITY STUDIES.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Camden,
New Jersey
081031505
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 424% from $2,269,729 to $11,903,446.
Coriell Institute For Medical Research was awarded
Epigenetic Therapies: New Approaches for Cancer Treatment
Project Grant P50CA254897
worth $11,903,446
from National Cancer Institute in August 2021 with work to be completed primarily in Camden New Jersey United States.
The grant
has a duration of 4 years 10 months and
was awarded through assistance program 93.397 Cancer Centers Support Grants.
The Project Grant was awarded through grant opportunity Specialized Programs of Research Excellence (SPOREs) in Human Cancers for years 2018, 2019 and 2020 (P50).
Status
(Ongoing)
Last Modified 7/21/25
Period of Performance
8/16/21
Start Date
6/30/26
End Date
Funding Split
$11.9M
Federal Obligation
$0.0
Non-Federal Obligation
$11.9M
Total Obligated
Activity Timeline
Transaction History
Modifications to P50CA254897
Additional Detail
Award ID FAIN
P50CA254897
SAI Number
P50CA254897-2306696807
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NC00 NIH National Cancer Institute
Funding Office
75NC00 NIH National Cancer Institute
Awardee UEI
XQJNZNQZAFP3
Awardee CAGE
1VFA6
Performance District
NJ-01
Senators
Robert Menendez
Cory Booker
Cory Booker
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Cancer Institute, National Institutes of Health, Health and Human Services (075-0849) | Health research and training | Grants, subsidies, and contributions (41.0) | $4,690,762 | 100% |
Modified: 7/21/25