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R01CA297080

Project Grant

Overview

Grant Description
TYK2 FUSIONS IN LYMPHOMA - PROJECT SUMMARY MALIGNANT LYMPHOMAS ARE A LEADING CAUSE OF CANCER DEATH RANKING 6TH AMONG MALIGNANCIES RESULTING IN MORTALITY. AMONG THESE, MATURE T-CELL LYMPHOMAS OFTEN EXHIBIT AN AGGRESSIVE CLINICAL COURSE AND THEIR PATHOGENESIS IS POORLY UNDERSTOOD. ALK-NEGATIVE ANAPLASTIC LARGE CELL LYMPHOMA (ALK-NEGATIVE ALCL) REPRESENTS A POORLY UNDERSTOOD CATEGORY OF MATURE T-CELL LYMPHOMAS. UNLIKE OTHER HEMATOPOIETIC MALIGNANCIES, RECURRENT GENETIC ALTERATIONS THAT HAVE BEEN EXPLOITED AS RATIONAL THERAPEUTIC TARGETS HAVE NOT BEEN DESCRIBED IN THESE TUMORS. WE DISCOVERED FOR THE FIRST TIME, RECURRENT TRANSLOCATIONS TARGETING THE INTRACELLULAR TYROSINE KINASE TYK2 IN ALK- NEGATIVE ALCL. IN THIS REGARD, WE IDENTIFIED A GENE FUSION JUXTAPOSING THE NUCLEOPHOSMIN (NPM1) GENE (5Q35) TO THE TYK2 GENE (19P13). NPM1 IS A NUCLEOLAR PHOSPHOPROTEIN INVOLVED IN SEVERAL ONCOGENIC GENE FUSIONS AND MUTATIONS IN CANCERS. NOTABLY, TYK2 WAS THE FIRST MEMBER OF THE JANUS ACTIVATING KINASE (JAK) FAMILY DESCRIBED AND PROPAGATES PHYSIOLOGIC CYTOKINE-DRIVEN SIGNALS AND IS CRITICAL FOR T-CELL PROLIFERATION AND DIFFERENTIATION. THE SIGNALING NETWORKS BY WHICH THE NPM1::TYK2 FUSION PROMOTES LYMPHOMAGENESIS ARE UNKNOWN. BASED ON OUR PRELIMINARY DATA, IT IS OUR CENTRAL HYPOTHESIS THAT NPM1::TYK2 IS AN ONCOGENIC DRIVER THAT PROMOTES THE DEVELOPMENT OF TCL, AND THAT THE KINASE ACTIVITY OF NPM1::TYK2 IS REQUIRED FOR ITS ONCOGENICITY. OUR PRELIMINARY RESULTS DEMONSTRATE THAT EXPRESSION OF THE RECURRENT NPM1::TYK2 FUSION IN CONDITIONAL TRANSGENIC MICE INDUCES LYMPHOMAS THAT RECAPITULATE THE MORPHOLOGIC AND GENETIC FEATURES OF TCL, SPECIFICALLY ALCL. THUS, THE MAIN GOAL OF THIS PROPOSAL IS TO INVESTIGATE THE IN VIVO ONCOGENICITY OF NPM1::TYK2 AND THE PATHWAYS OF NPM1::TYK2- INDUCED LYMPHOMAGENESIS. THE OVERALL IMPACT OF THIS PROPOSAL IS TO ADVANCE UNDERSTANDING OF THE MECHANISMS BY WHICH ONCOGENIC TYK2 CAUSES LYMPHOMA AND IDENTIFY CURRENTLY UNKNOWN DOWNSTREAM SIGNALING MODULES WHICH MAY SERVE AS VULNERABILITY TARGETS FOR NOVEL PRECISION THERAPY FOR ONCOGENIC TYK2-DRIVEN CANCERS.
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)
Place of Performance
New York United States
Geographic Scope
State-Wide
Sloan-Kettering Institute For Cancer Research was awarded TYK2 Fusions in Lymphoma: Investigating Oncogenic Pathways Precision Therapy Project Grant R01CA297080 worth $3,111,184 from National Cancer Institute in September 2025 with work to be completed primarily in New York United States. The grant has a duration of 4 years and was awarded through assistance program 93.396 Cancer Biology Research. The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).

Status
(Ongoing)

Last Modified 9/5/25

Period of Performance
9/1/25
Start Date
8/31/29
End Date
0% Complete

Funding Split
$3.1M
Federal Obligation
$0.0
Non-Federal Obligation
$3.1M
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to R01CA297080

Additional Detail

Award ID FAIN
R01CA297080
SAI Number
R01CA297080-2420996294
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
KUKXRCZ6NZC2
Awardee CAGE
6X133
Performance District
NY-90
Senators
Kirsten Gillibrand
Charles Schumer
Modified: 9/5/25