R35CA253059
Project Grant
Overview
Grant Description
P53-Mediated Metabolic Regulation in Tumor Suppression - Project Summary
Inactivation of the P53 tumor suppressor is a pivotal event in the formation of most human cancers. P53 acts as a transcription factor to modulate various types of cellular processes to suppress cancer development. Although the classic activities of P53, including cell-cycle arrest, senescence, and apoptosis, serve as critical barriers to cancer development, accumulating evidence suggests that other unconventional mechanisms, such as metabolic regulation, are also critically involved in suppressing tumor growth.
Nevertheless, despite the fact that the role of the P53 pathway in tumor suppression is indisputable, it remains a daunting task to target this pathway for cancer therapy. The main issue is whether activation of P53 function in vivo leads to significant tumor regression without causing serious toxicity in normal tissues.
Cancer cells rewire cellular metabolism to meet the energetic and substrate demands of tumor development, but this rewiring also creates metabolic vulnerabilities specific to cancer cells. By taking advantage of these metabolic vulnerabilities, our preliminary studies showed that specific activation of the tumor suppression function of P53 through certain metabolic targets can be effective in suppressing tumor growth but apparently does not cause severe harm to normal tissues.
The central objective of the proposed research plan is to comprehensively define the P53-mediated metabolic regulation program that is required for its tumor suppression as a means to identify new targets/pathways for therapy. Toward this end, our research program will be based on two complementary lines of research aiming to further dissect: 1) P53-mediated metabolic pathways required for its tumor suppression; 2) the novel ferroptosis pathway regulated by P53 and the effects in both normal and cancer cells.
We expect that the research program described above will identify specific targets to suppress tumor growth but have minimal or at least manageable toxicity in normal tissues.
Inactivation of the P53 tumor suppressor is a pivotal event in the formation of most human cancers. P53 acts as a transcription factor to modulate various types of cellular processes to suppress cancer development. Although the classic activities of P53, including cell-cycle arrest, senescence, and apoptosis, serve as critical barriers to cancer development, accumulating evidence suggests that other unconventional mechanisms, such as metabolic regulation, are also critically involved in suppressing tumor growth.
Nevertheless, despite the fact that the role of the P53 pathway in tumor suppression is indisputable, it remains a daunting task to target this pathway for cancer therapy. The main issue is whether activation of P53 function in vivo leads to significant tumor regression without causing serious toxicity in normal tissues.
Cancer cells rewire cellular metabolism to meet the energetic and substrate demands of tumor development, but this rewiring also creates metabolic vulnerabilities specific to cancer cells. By taking advantage of these metabolic vulnerabilities, our preliminary studies showed that specific activation of the tumor suppression function of P53 through certain metabolic targets can be effective in suppressing tumor growth but apparently does not cause severe harm to normal tissues.
The central objective of the proposed research plan is to comprehensively define the P53-mediated metabolic regulation program that is required for its tumor suppression as a means to identify new targets/pathways for therapy. Toward this end, our research program will be based on two complementary lines of research aiming to further dissect: 1) P53-mediated metabolic pathways required for its tumor suppression; 2) the novel ferroptosis pathway regulated by P53 and the effects in both normal and cancer cells.
We expect that the research program described above will identify specific targets to suppress tumor growth but have minimal or at least manageable toxicity in normal tissues.
Funding Goals
TO PROVIDE FUNDAMENTAL INFORMATION ON THE CAUSE AND NATURE OF CANCER IN PEOPLE, WITH THE EXPECTATION THAT THIS WILL RESULT IN BETTER METHODS OF PREVENTION, DETECTION AND DIAGNOSIS, AND TREATMENT OF NEOPLASTIC DISEASES. CANCER BIOLOGY RESEARCH INCLUDES THE FOLLOWING RESEARCH PROGRAMS: CANCER CELL BIOLOGY, CANCER IMMUNOLOGY, HEMATOLOGY AND ETIOLOGY, DNA AND CHROMOSOMAL ABERRATIONS, TUMOR BIOLOGY AND METASTASIS, AND STRUCTURAL BIOLOGY AND MOLECULAR APPLICATIONS.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
New York,
New York
100323802
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 666% from $570,812 to $4,371,332.
The Trustees Of Columbia University In The City Of New York was awarded
P53 Metabolic Regulation for Tumor Suppression
Project Grant R35CA253059
worth $4,371,332
from National Cancer Institute in September 2021 with work to be completed primarily in New York New York United States.
The grant
has a duration of 7 years and
was awarded through assistance program 93.396 Cancer Biology Research.
The Project Grant was awarded through grant opportunity NCI Outstanding Investigator Award (R35 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 8/20/25
Period of Performance
9/1/21
Start Date
8/31/28
End Date
Funding Split
$4.4M
Federal Obligation
$0.0
Non-Federal Obligation
$4.4M
Total Obligated
Activity Timeline
Transaction History
Modifications to R35CA253059
Additional Detail
Award ID FAIN
R35CA253059
SAI Number
R35CA253059-161644501
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NC00 NIH National Cancer Institute
Funding Office
75NC00 NIH National Cancer Institute
Awardee UEI
QHF5ZZ114M72
Awardee CAGE
3FHD3
Performance District
NY-13
Senators
Kirsten Gillibrand
Charles Schumer
Charles Schumer
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) | $1,905,120 | 100% |
Modified: 8/20/25