Project Grant R01CA292071
- This $683,472 Project Grant awarded by the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) supports the development of a novel targeted therapy for acute myeloid leukemia (AML). The principal investigators at the University of Cincinnati are conducting preclinical research to evaluate a differentiation-inducing agent (HOSU-53) that targets the mitochondrial enzyme DHODH. The goal is to promote AML cell differentiation, activate the immune system, and induce ferroptosis to...
- This Project Grant award from the National Cancer Institute (NCI), under the federal Cancer Biology Research program (CFDA 93.396), provides $487,542 to the Beckman Research Institute of the City of Hope to conduct research aimed at understanding the role of mitochondrial RNA methylation in acute myeloid leukemia (AML), particularly for high-risk AML subtypes. The key objectives are to determine the functional importance of the mitochondrial methyltransferase METTL17 in AML pathogenesis, dissect...
- The project "ENGINEERING NATURAL KILLER CELLS TO TARGET ACUTE MYELOID LEUKEMIA WITH HLA-DR LOSS" is being funded by a $429,000 Project Grant from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) awarded to Western University of Health Sciences in California. The goal of this 3-year research project is to develop a novel chimeric antigen receptor (CAR) natural killer (NK) cell therapy that can specifically target acute myeloid leukemia (AML) with loss of the...
- This Project Grant award of $502,516 from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) supports research at Case Western Reserve University focused on developing a small-molecule degrader called SISU-102 to target leukemic stem cells (LSCs) in acute myeloid leukemia (AML). The key objectives are to further investigate the impacts of these HSF1 degraders on LSC self-renewal, identify sensitive and resistant AML subtypes, and explore the underlying mechanisms. This...
- The National Cancer Institute (NCI), under the Cancer Biology Research federal grant program (CFDA 93.396), awarded a $530,106 Project Grant to the Children's Hospital Medical Center in Cincinnati, Ohio. The grant, awarded on September 11, 2025, supports research aimed at understanding and targeting polyamine metabolism in leukemia stem cells (LSCs) to improve outcomes for patients with acute myeloid leukemia (AML). The overarching goal is to develop LSC-directed therapies that can help overcome...
- This Project Grant award from the National Cancer Institute (CFDA 93.396 - Cancer Biology Research) provides funding to Case Western Reserve University to conduct research aimed at understanding the fundamental biological mechanisms of acute myeloid leukemia (AML) and developing new therapeutic approaches. The $491,357 award supports investigations into using proteasome inhibitors and an mTORC1 activator molecule to induce metabolic stress and resensitize AML cells to treatment, particularly...
- This federal Project Grant award from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) provides $734,435.00 in funding to the Beckman Research Institute of the City of Hope to conduct research aimed at overcoming resistance to BH3 mimetic drugs in the treatment of acute myeloid leukemia (AML), particularly in older patients. The key objectives are to define the molecular mechanisms underlying BH3 mimetic resistance in AML and evaluate whether targeting the ADSS2 enzyme,...
- This Project Grant award from the National Cancer Institute (CFDA 93.396 - Cancer Biology Research) provides $439,644 to The Leland Stanford Junior University to conduct functional studies on human acute myeloid leukemia (AML) stem cells. The key objectives are to: 1) Investigate the relationship between specific genetic mutations and AML stem cell frequency, disease initiation, and disease maintenance by correcting mutations in primary AML cells and AML-induced pluripotent stem cells (iPSCs);...
- This $220,018 federal Project Grant award from the National Cancer Institute's Cancer Treatment Research program (CFDA 93.395) supports research to determine the role of mitochondrial metabolism and dynamics in the regulation of chemotherapy-induced reactive myelopoiesis and associated pro-metastatic effects. The University of Louisville will conduct this 2-year research project to investigate how chemotherapy-induced changes in hematopoietic stem and progenitor cell mitochondrial function,...
- This Project Grant award from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) supports research to develop a targeted therapy for acute myeloid leukemia (AML) with the chromosome inversion inv(16). The $545,170 award to Versiti Wisconsin, Inc. aims to characterize the mechanisms by which the oncogenic fusion protein CBFB-SMMHC activates the translation initiation factor EIF4G1, leading to AML transformation. The research will test whether inhibiting EIF4G1 can overcome...
TARGETING MITOCHONDRIAL CALCIUM TO ERADICATE LEUKEMIA-INITIATING CELLS - SUMMARY THE GOAL OF THIS PROJECT IS TO DEVELOP STRATEGIES FOR THE ERADICATION OF LEUKEMIA-INITIATING CELLS (LICS) IN AML PATIENTS WHO HAVE RECEIVED INITIAL THERAPY WITH VENETOCLAX AND AZACITIDINE (VEN/AZA). AS DEMONSTRATED PREVIOUSLY, ALMOST ALL AML PATIENTS TREATED WITH VEN/AZA WILL EVENTUALLY RELAPSE. THUS, PROVIDING IMPROVED THERAPEUTIC REGIMENS IS AN URGENT UNMET NEED. OUR PREVIOUS STUDIES HAVE DEMONSTRATED THAT MORE THAN ONE SUBTYPE OF LIC CAN EXIST SIMULTANEOUSLY IN THE SAME PATIENT. IMPORTANTLY, DIFFERENT LIC SUBTYPES CAN DEMONSTRATE HIGHLY VARIABLE RESPONSES TO THERAPY, INCLUDING RESISTANCE TO VEN/AZA. THUS, LIC HETEROGENEITY MAY BE A PREVALENT FEATURE OF AML BIOLOGY, AND AS SUCH POSES A SIGNIFICANT CHALLENGE IN DESIGNING OPTIMAL THERAPIES THAT EFFECTIVELY ERADICATE THEM. CONSEQUENTLY, A MAJOR GOAL OF THIS PROJECT IS TO CHARACTERIZE AND TARGET VEN/AZA RESISTANT LICS. OUR PRELIMINARY DATA INDICATE THAT RELIANCE ON UPTAKE OF CALCIUM INTO MITOCHONDRIA IS A DISTINCT FEATURE AND VULNERABILITY OF VEN/AZA RESISTANT AML CELLS. THUS, WE HAVE INVESTIGATED THE ROLE OF THE CALCIUM UNIPORTER, MCU, AS A POTENTIAL THERAPEUTIC TARGET. OUR FINDINGS SHOW THAT BOTH GENETIC AND PHARMACOLOGICAL INHIBITION OF MCU IS HIGHLY CYTOTOXIC TO VEN/AZA RESISTANT LICS. IMPORTANTLY, NORMAL HEMATOPOIETIC STEM/PROGENITOR CELLS DO NOT SHARE THIS EXTENSIVE RELIANCE UPON MCU FOR MITOCHONDRIAL METABOLISM AND SURVIVAL. THUS, THIS AXIS APPEARS TO REPRESENT A UNIQUE FEATURE OF VEN/AZA-RESISTANT LIC AND IN TURN, AN ATTRACTIVE OPPORTUNITY FOR THERAPEUTIC INTERVENTION. TO TRANSLATE THIS STRATEGY TO CLINICAL PRACTICE, WE HAVE LEVERAGED A RECENT FINDING THAT SHOWS THE WELL CHARACTERIZED CHEMOTHERAPY AGENT, MITOXANTRONE (MITOX), IS A STRONG INHIBITOR OF MCU. INTRIGUINGLY, WE DEMONSTRATE THAT MITOX IS EFFECTIVE IN SUPPRESSING MITOCHONDRIAL CALCIUM UPTAKE AND DOWNSTREAM METABOLISM AT DOSES 10-100 FOLD LOWER THAN USED FOR CONVENTIONAL CHEMOTHERAPY PURPOSES. INDEED, AT DOSES AS LOW AS 10NM, WE OBSERVE POTENT ERADICATION OF VEN/AZA RESISTANT LICS, WITH NO EVIDENCE OF DNA DAMAGE, AND NO DISCERNABLE EFFECT ON THE GROWTH OF NORMAL HEMATOPOIETIC STEM/PROGENITOR CELLS. BASED ON THESE FINDINGS, OUR GOALS ARE TO: 1) PERFORM PRECLINICAL MODELING STUDIES AS A PRELUDE TO CLINICAL INVESTIGATION AND TO BETTER UNDERSTAND THE MITOX MECHANISM OF ACTION, 2) CONDUCT A CLINICAL TRIAL USING LOWER-DOSE MITOX IN COMBINATION WITH VEN/AZA AS A STRATEGY TO TARGET DRUG-RESISTANT LICS AND THEREBY INCREASE REMISSION DURATION, AND 3) TO PERFORM A DETAILED IN VIVO ANALYSIS OF LIC SUBTYPES IN PATIENTS UNDERGOING VEN/AZA/MITOX THERAPY TO BETTER DEFINE THE ROLE OF MITOCHONDRIAL CALCIUM UPTAKE AND ANY OTHER MOLECULAR EVENTS THAT CONTRIBUTE TO THERAPY RESISTANCE IN THE HETEROGENOUS LIC COMPARTMENT. TAKEN TOGETHER, THE PROPOSED STUDIES WILL PROVIDE A COMPREHENSIVE EVALUATION OF MITOX AS A CLINICAL STRATEGY TO AUGMENT VEN/AZA THERAPY AND WILL DETERMINE THE PREVALENCE AND ROLE OF CALCIUM UPTAKE IN THE BIOLOGY OF DRUG RESISTANT LICS.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $437.4k | 8/1/25 | ||
| Not listed | $437.4k | 7/30/24 |