R35CA253183
Project Grant
Overview
Grant Description
Oncogenic Mechanisms, Molecular Stratification, and Therapeutic Targets of Brain Tumors - Abstract
The work to be pursued in this application will continue and expand the program pioneered by Dr. Iavarone to combine innovative computational tools and state-of-the-art experimental cancer models in vitro and in vivo. The goal is to identify homogeneous subgroups of cancer patients in order to dissect the pathogenesis of cancer and design tailored and fully validated personalized therapeutic approaches. The application is focused on glioblastoma multiforme, one of the most lethal forms of human cancer.
The investigation of glioblastoma has represented a long-standing effort of Dr. Iavarone's laboratory, which in recent work has produced novel targeted therapeutic opportunities currently being tested in clinical studies. The proposal will also benefit from the organizational contexts recently set in motion by the large network operations coordinated by the PI.
The research plan is articulated around the development of a novel and integrated computational-experimental framework for:
I) The identification of homogeneous groups of tumors sharing activation of the same biological pathways;
II) The study of cancer heterogeneity at the single-cell level to accurately inform tumor classifications;
III) The therapeutic prediction emerging from the identification of driver modules and synthetic lethal relationships of malignant glioma.
We will develop and apply novel technologies for high-throughput transcriptomic and proteomic analysis of individual cells within malignant glioma tissues. These approaches, which we have pioneered in our laboratory at Columbia University during the last few years, will serve as the basis for the multifaceted computational analysis that will extract genes and proteins responsible for the phenotypic state of individual cells.
Experimental validations will be selectively applied to the novel and most exciting molecular pathways and will be performed by our laboratory, which has an array of experimental tools and sequence-annotated patient-derived models to pursue each individual question. As for the selection of oncogene-dependent and independent vulnerabilities identified by our previous work, the ability of our studies to identify novel driver phenotypes and master regulators of individual tumor cells will be geared towards routing the new mechanisms into pathway-based synthetic lethality that will inform specific drug sensitivities.
The successful outcome of this proposal is an integrated computational-experimental pipeline that will be able to mechanistically identify the determinants of tumor genomes and phenotypes of solid tumors. This information will be of invaluable significance to decipher evolving tumor dependencies and provide the most accurate therapeutic predictions.
The work to be pursued in this application will continue and expand the program pioneered by Dr. Iavarone to combine innovative computational tools and state-of-the-art experimental cancer models in vitro and in vivo. The goal is to identify homogeneous subgroups of cancer patients in order to dissect the pathogenesis of cancer and design tailored and fully validated personalized therapeutic approaches. The application is focused on glioblastoma multiforme, one of the most lethal forms of human cancer.
The investigation of glioblastoma has represented a long-standing effort of Dr. Iavarone's laboratory, which in recent work has produced novel targeted therapeutic opportunities currently being tested in clinical studies. The proposal will also benefit from the organizational contexts recently set in motion by the large network operations coordinated by the PI.
The research plan is articulated around the development of a novel and integrated computational-experimental framework for:
I) The identification of homogeneous groups of tumors sharing activation of the same biological pathways;
II) The study of cancer heterogeneity at the single-cell level to accurately inform tumor classifications;
III) The therapeutic prediction emerging from the identification of driver modules and synthetic lethal relationships of malignant glioma.
We will develop and apply novel technologies for high-throughput transcriptomic and proteomic analysis of individual cells within malignant glioma tissues. These approaches, which we have pioneered in our laboratory at Columbia University during the last few years, will serve as the basis for the multifaceted computational analysis that will extract genes and proteins responsible for the phenotypic state of individual cells.
Experimental validations will be selectively applied to the novel and most exciting molecular pathways and will be performed by our laboratory, which has an array of experimental tools and sequence-annotated patient-derived models to pursue each individual question. As for the selection of oncogene-dependent and independent vulnerabilities identified by our previous work, the ability of our studies to identify novel driver phenotypes and master regulators of individual tumor cells will be geared towards routing the new mechanisms into pathway-based synthetic lethality that will inform specific drug sensitivities.
The successful outcome of this proposal is an integrated computational-experimental pipeline that will be able to mechanistically identify the determinants of tumor genomes and phenotypes of solid tumors. This information will be of invaluable significance to decipher evolving tumor dependencies and provide the most accurate therapeutic predictions.
Awardee
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
Miami,
Florida
331361013
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 539% from $663,188 to $4,236,215.
University Of Miami was awarded
Brain Tumor Molecular Targets & Therapies
Project Grant R35CA253183
worth $4,236,215
from National Cancer Institute in September 2021 with work to be completed primarily in Miami Florida 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
9/24/21
Start Date
8/31/28
End Date
Funding Split
$4.2M
Federal Obligation
$0.0
Non-Federal Obligation
$4.2M
Total Obligated
Activity Timeline
Transaction History
Modifications to R35CA253183
Additional Detail
Award ID FAIN
R35CA253183
SAI Number
R35CA253183-2010470083
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
F8THLJQSAF93
Awardee CAGE
9B962
Performance District
FL-26
Senators
Marco Rubio
Rick Scott
Rick Scott
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) | $1,777,345 | 100% |
Modified: 8/20/25