Who We Fund

Regents of the University of Michigan

I am a Research Scientist in the Deininger Lab at Versiti Blood Research Institute, where my work focuses on leukemia biology—particularly in hematopoietic stem and progenitor cells, mitochondrial function, and the identification of therapeutic targets in hematologic malignancies. I have extensive experience in experimental hematology, including stem cell assays, CRISPR-based genome editing, lentiviral and retroviral modeling, and advanced flow cytometry.

In my current role, I have led projects optimizing functional metabolic assays, such as Seahorse XF analysis, to study mitochondrial bioenergetics in rare stem cell populations. I also work extensively with mouse models of leukemia, including xenografts, and coordinate multi-institutional collaborations for biospecimen acquisition and translational research.

In August 2025, I will transition with the Deininger Lab to the University of Michigan, where I will hold a Research Assistant Professor appointment in the Department of Internal Medicine, Division of Hematology/Oncology. My goal is to continue bridging mechanistic studies with preclinical testing to develop and refine targeted therapies for hematologic malignancies.

Program Name(s)

Career Development Program

Project Title

Understanding the role of Metabolic Regulator SIRT5 in Acute Lymphoblastic Leukemia

Albert Einstein College of Medicine

Dr. Konopleva is a Director of the Acute Leukemia Program and a Co-Director of the Translational Blood Cancer Institute at Einstein/Montefiore Cancer Center, NY. The PI is a physician-scientist with an active clinical practice where she treats MDS/AML patients on a routine basis outpatient and inpatient. She directs laboratory studying at understanding the pathogenesis and chemoresistance of AML and MDS stem/progenitor cells, with focus on metabolic and apoptosis regulators. Dr. Konopleva has joined Montefiore-Einstein in summer 2022 after long successful career as a physician-scientist at M.D. Anderson Cancer Center in Houston, Texas. She has brought multiple targeted agents from pre-clinical investigations into clinical trials, most notable BCL-2 inhibitor Venetoclax which in combination with low-intensity therapies has become a standard of care for older AML patients unfit for intensive chemotherapy and is being studied in high-risk MDS.

Program Name(s)

Discovery

Project Title

Targeting metabolic reprogramming in MDS and AML stem/progenitor cells

University of Colorado Denver, Anschutz Medical Campus

Dr. Collins is an Assistant Professor in the Division of Hematology at the University of Colorado Anschutz Medical Campus, where she leads a translational research program studying the mechanisms of preleukemic transformation in myeloid malignancies. Following her undergraduate studies at Williams College, Dr. Collins received her MD/PhD from the University of Michigan, where she worked with Dr. Jay Hess studying the role of collaborator proteins in HOXA9-mediated leukemic transformation. She then completed residency and fellowship training in Hematology/Oncology at Stanford, where she completed her postdoctoral research training in Dr. Ravi Majeti’s lab. Her current research focuses on understanding how combinations of genetic mutations alter hematopoietic stem cell function and drive progression from preleukemic states to aggressive myeloid malignancies, such as AML and CMML. Using engineered human stem cell models and primary patient samples, her work aims to identify mechanisms of leukemic transformation and therapeutic vulnerabilities that can be targeted early in disease evolution.

Program Name(s)

Career Development Program

Project Title

Investigating the role of preleukemia duration and clonal burden in progression to AML

Perelman School of Medicine at the University of Pennsylvania

Jalpa Doshi, PhD, is a Professor at the University of Pennsylvania and Director of Value Based Insurance Design Initiatives at the Center for Health Incentives and Behavioral Economics. Her research program aims to advance our understanding of how pharmaceuticals can be better accessed and utilized in the health care system to improve health outcomes while balancing costs. She has been a national leader in applying powerful health economics, outcomes research, and policy methods to address issues related to pharmaceutical access, costs, outcomes, and value. Her research has received widespread attention from the media including the New York Times and the Wall Street Journal and has directly influenced policies of public and private insurers. For example, she was the first to produce rigorous empirical research advocating for the closure of the “donut hole” (executed under the Affordable Care Act) and institution of an annual out-of-pocket maximum with “smoothing” (executed under the Inflation Reduction Act) under Medicare Part D. Her work documenting negative consequences of cost sharing among veterans was cited in arguments that kept the VA from increasing drug copayments. Her research on the burden of prior authorization policies for novel cholesterol-lowering agents was used to work with national insurers to appropriately reduce their policy restrictions. In recognition of her work, she has received numerous awards and honors from national and international organizations.

Program Name(s)

Equity in Access

Project Title

Impact of Insurance Type and Cost Sharing on Equity in Access to Oral Anticancer Medications for Blood Cancers

The Brigham and Women’s Hospital

My scientific background involves the functional characterization of rare immune cells called dendritic cells in advanced melanoma patients. These cells are master regulators of immunity and are responsible for orchestrating anti-cancer responses driven by effector cells called T cells. My PhD focused on patients who received immunotherapy via antibodies that reinvigorate the immune system, also known as immune checkpoint inhibitors. I collected patient blood samples before and during treatment, and found that a critical subtype of dendritic cell is numerically and functionally impaired in patients who did not respond to immunotherapy compared to those who responded. In my current lab, I leveraged my experience in immune cell research and now study how a novel drug combination can be used to target and kill acute myeloid leukemia (AML) cells. This innovative approach targets two biologically important processes within a cell – the protein-making machinery and the control of cell death.

Program Name(s)

Career Development Program

TAP Partner

Rgenta Therapeutics is developing a pipeline of oral, small-molecule RNA-targeting medicines with an initial focus on oncology and neurological disorders. Rgenta has a proprietary platform to mine the massive genomics data to identify targetable RNA processing events and to design small-molecule glues to modulate the interactions among the spliceosome, regulatory proteins, and RNAs. 

Rgenta is working closely with TAP to further develop RNA-targeting molecules by supporting preclinical studies with the goal of moving towards clinical development in hematological malignancies. 

Program Name(s)

Therapy Acceleration Program

Project Title

Supporting development of RNA-targeting molecules for blood cancers

Dana-Farber Cancer Institute

Program Name(s)

Career Development Program

Project Title

Mechanisms of oncogenic transcription in NPM1-mutant myeloid leukemia

TAP Partner

Dimericon is a private biotech company focused on exploring crosslinked helix dimers (Dimericons) as therapeutics and templates for small molecule development. Dimericon’s technology targets hard-to-drug intracellular protein-protein interactions using rationally designed mimetics of helix dimers. The Seed round of financing will support preclinical studies to further develop the current cFLIP inhibitor lead compound, DMRX1004, to be an IND ready clinical candidate in hematological malignancies.

Program Name(s)

Therapy Acceleration Program

Project Title

Supporting development of dimericons (crosslinked helix dimers) for blood cancers

Imperial College, University of London

After completing a PhD in Immunology at Trinity College Dublin, I moved to Imperial College London to study how persistent infection with a virus causes Leukemia, Lymphoma and other diseases. The virus in question is Human T cell leukemia virus type-1 (HTLV-1), which infects the very cells which defend us against viruses: T cells. Around 5% of virus-carriers develop aggressive blood cancer (Adult T cell leukemia/lymphoma, ATL), in which one infected T cell becomes malignant. ATL is very difficult to treat, and people with the most aggressive forms survive for less than a year. I made the game-changing discovery that ATL-like T cells circulate in the blood of carriers who go on to develop ATL years before they show symptoms of ATL. I am now developing new diagnostics which can detect ATL early, and together with clinicians at the U.K. National Centre for Human Retrovirology and the Memorial Sloan Kettering Cancer Centre, will test whether a recently licenced drug can eliminate ATL-like T cells in high-risk carriers.

Program Name(s)

Translational Research Program

Project Title

Detection and treatment of Adult T cell leukemia/lymphoma in the premalignant stage.

Monash University

Professor Jake Shortt is a clinician scientist who is co-appointed by Monash Health as Director of Clinical Haematology and by Monash University as the Head of Haematology Research at the School of Clinical Sciences. Monash Health provides lymphoma services to the largest Australian healthcare network in the Australian state of Victoria. He is also an Honorary Clinical Professor at the Sir Peter MacCallum Department of Oncology, University of Melbourne.

Professor Shortt is group leader of the 'Blood Cancer Therapeutics Laboratory' at Monash, seeking to discover and translate new lymphoma treatments to the clinic. As a clinician scientist his research covers the full translational spectrum from scientific discovery to advanced clinical trials and registry initiatives. For more than a decade his research has focussed on poor-risk lymphoid cancers, particularly those hallmarked by activation of a gene called 'MYC' which features in some of the most aggressive lymphomas.

Program Name(s)

Translational Research Program

Project Title

Exploiting escape from Y-inactivation as a synthetic dependency in MYC-driven lymphoma

Dana-Farber Cancer Institute

Margaret Shipp, MD, is Chief of the Division of Hematologic Neoplasia at Dana-Farber Cancer Institute and a Professor of Medicine at Harvard Medical School. Her research focuses on the clinical and molecular heterogeneity of the large B-cell lymphomas (LBCLs) and Hodgkin lymphomas. Dr. Shipp has led efforts to define molecular signatures of LBCLs and Hodgkin lymphomas, identify biologically distinct subsets of these diseases, and characterize associated rational treatment targets including modulators of the host anti-tumor immune response.

Program Name(s)

Translational Research Program

Project Title

Analysis and Targeting of Tumor-Associated Monocytes/Macrophages that Inhibit PD-1 Blockade

TAP Partner

Caribou is a clinical-stage biotechnology company, co-founded by CRISPR pioneer and Nobel Prize winner Jennifer Doudna, Ph.D., using next-generation CRISPR genome-editing technology to develop “off-the-shelf” (allogeneic) CAR therapies for hard-to-treat blood cancers.

Program Name(s)

Therapy Acceleration Program

Project Title

A phase 1 study of CB-010, a CRISPR-edited allogeneic CAR-T targeting CD19, in patients with B-cell NHL

A phase 1 study of CB-011, a CRISPR-edited allogeneic CAR-T targeting BCMA, in patients with multiple myeloma