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UM1CA294119

Cooperative Agreement

Overview

Grant Description
Targeting transcriptional addiction in fusion-driven sarcoma - 7. Project summary/abstract

The overarching goal of this NGC center is to leverage expertise in small molecule drug discovery, target identification, and protein and IDR biochemistry to identify and advance small molecules that target transcriptional fusion oncoproteins by 1) targeting the transcriptional machinery that is co-opted by fusion proteins to drive the oncogenic transcriptional programs, and 2) directly impair IDR function with small molecules.

Transcriptional fusion proteins induce oncogenic gene expression programs that drive cancer development and progression.

These proteins act as neomorphic transcription factors by recruiting and re-wiring transcriptional regulatory complexes.

Rational drug design to directly target transcriptional fusion proteins remains a major challenge because these proteins lack enzymatic activity and do not have obvious pockets amenable for small molecule binding.

In addition, the mechanisms by which fusion oncoproteins co-opt transcriptional regulatory complexes are incompletely understood.

As such, the development of new therapies to target transcriptional fusion proteins has lagged efforts to develop targeted therapies for mutant oncoproteins involved in cellular signaling.

Our team has discovered that the Mediator transcriptional co-activator complex is co-opted to control the oncogenic gene expression programs induced by transcriptional fusion proteins.

We have further identified the CDK8 kinase module as a druggable entry point by which to impair Mediator function through a novel trapping mechanism.

Our team will probe the biochemical and transcriptional mechanisms through which CDK8/19 inhibitors alter Mediator function and develop CDK8/19 inhibitors that maximize Mediator impairment and study these small molecules in advanced preclinical models of Ewing sarcoma and rhabdomyosarcoma.

We further identified that Vaccinia-related kinase 1 (VRK1) is a kinase that becomes synthetically lethal following CDK8/19 impairment, and our team will develop novel specific VRK1 inhibitors and evaluate their efficacy in single agent and combination strategies.

A central theme has recently emerged that many fusion proteins consist of a DNA binding domain linked to an intrinsically disordered region (IDR).

The IDR mediates self-association or phase separation that has been shown to be essential for the oncogenic nature of these fusion proteins.

Our team has developed an innovative biochemical method of identifying the key protein regions within IDRs that mediate self-association.

We will map the key self-association residues in three fusion protein IDRs and identify small molecules that impair the ability of these regions to drive phase separation.
Funding Goals
TO DEVELOP THE MEANS TO CURE AS MANY CANCER PATIENTS AS POSSIBLE AND TO CONTROL THE DISEASE IN THOSE PATIENTS WHO ARE NOT CURED. CANCER TREATMENT RESEARCH INCLUDES THE DEVELOPMENT AND EVALUATION OF IMPROVED METHODS OF CANCER TREATMENT THROUGH THE SUPPORT AND PERFORMANCE OF BOTH FUNDAMENTAL AND APPLIED LABORATORY AND CLINICAL RESEARCH. RESEARCH IS SUPPORTED IN THE DISCOVERY, DEVELOPMENT, AND CLINICAL TESTING OF ALL MODES OF THERAPY INCLUDING: SURGERY, RADIOTHERAPY, CHEMOTHERAPY, AND BIOLOGICAL THERAPY INCLUDING MOLECULARLY TARGETED THERAPIES, BOTH INDIVIDUALLY AND IN COMBINATION. IN ADDITION, RESEARCH IS CARRIED OUT IN AREAS OF NUTRITIONAL SUPPORT, STEM CELL AND BONE MARROW TRANSPLANTATION, IMAGE GUIDED THERAPIES AND STUDIES TO REDUCE TOXICITY OF CYTOTOXIC THERAPIES, AND OTHER METHODS OF SUPPORTIVE CARE THAT MAY SUPPLEMENT AND ENHANCE PRIMARY TREATMENT. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO EXPAND AND IMPROVE THE SBIR PROGRAM, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Place of Performance
Dallas, Texas 753907208 United States
Geographic Scope
Single Zip Code
Analysis Notes
Amendment Since initial award the total obligations have increased 107% from $2,203,647 to $4,553,009.
The University Of Texas Southwestern Medical Center was awarded Transcriptional Fusion Protein Targeting for Sarcoma Treatment Cooperative Agreement UM1CA294119 worth $4,553,009 from National Cancer Institute in July 2024 with work to be completed primarily in Dallas Texas United States. The grant has a duration of 5 years and was awarded through assistance program 93.395 Cancer Treatment Research. The Cooperative Agreement was awarded through grant opportunity Next Generation Chemistry Centers for Fusion Oncoproteins (UM1 Clinical Trial Not Allowed).

Status
(Ongoing)

Last Modified 7/21/25

Period of Performance
7/8/24
Start Date
6/30/29
End Date
25.0% Complete

Funding Split
$4.6M
Federal Obligation
$0.0
Non-Federal Obligation
$4.6M
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to UM1CA294119

Transaction History

Modifications to UM1CA294119

Additional Detail

Award ID FAIN
UM1CA294119
SAI Number
UM1CA294119-2949957814
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NC00 NIH National Cancer Institute
Funding Office
75NC00 NIH National Cancer Institute
Awardee UEI
YZJ6DKPM4W63
Awardee CAGE
1CNP4
Performance District
TX-30
Senators
John Cornyn
Ted Cruz
Modified: 7/21/25