Who We Fund

The University of Melbourne

Professor Dawson is the Associate Director for Research Translation, a Program Head in Laboratory Research and a Consultant Haematologist at the Peter MacCallum Cancer Centre. His research interest is studying the role of epigenetic regulators in the initiation, maintenance and progression of cancer. His current research spans cell and molecular biology, functional genomics, cancer immunology, chemical biology and clinical translation. He is the Sir Edward Dunlop Fellow for the Cancer Council of Victoria and a HHMI International Research Scholar. In recognition of his research achievements, he has been elected to the Australian Academy of Science, the Australian Academy of Health and Medical Sciences and an EMBO member. He has received several prestigious awards including the McCulloch & Till Award from the International Society of Experimental Haematology, the Jacques Miller Medal from the Australian Academy of Science and the Prime Minister’s Prize as Life Scientist in 2020.

Program Name(s)

Translational Research Program

Project Title

Understanding molecular determinants of immune evasion to CAR-T cells at single clone resolution

The University of Texas Southwestern Medical Center

I am an NIH-funded physician scientist with a scientific and clinical focus on cutaneous lymphomas. We have utilized high-dimensional genomic, epigenetic, and immunological approaches to elucidate the immunobiology of multiple cutaneous T and B cell lymphomas. We utilize a combination of human and mouse models as well as a number of unbiased approaches including whole genome sequencing, bulk and single cell RNA and ATAC-Seq, epigenetic assays such as ATAC-Seq, CUT&RUN, and HiCHIP, as well as spectral flow and multimodal CITE-Seq. These efforts have led to manuscripts published in Nature, Nature Cancer, Cancer Discovery, and Blood. These efforts have been funded by an NIH Director’s New Innovator Award, the Damon Runyon Foundation, the Doris Duke Charitable Foundation, and most recently the Mark Foundation for Cancer Research.

Program Name(s)

Career Development Program

Project Title

Identification of novel therapeutic strategies for aggressive subtypes of CTCL

Yale University

Markus Müschen, MD-PhD, is a physician-scientist at Yale University, where he serves as the Director of the Center of Molecular and Cellular Oncology and Chief of the Division of Basic Science of Yale Cancer Center. His research focuses on signal transduction and metabolic pathways in lymphoid malignancies and how they can be intercepted for the treatment of drug-resistant leukemia and lymphoma. Markus Müschen studied Medicine in Cologne, Germany and the Institut Pasteur in Paris, France. After his clinical training in hematology-oncology with Volker Diehl, he completed postdoctoral fellowships with Klaus Rajewsky and Janet Rowley. Before coming to Yale, Markus Müschen’s laboratory was at UCSF for seven years where he led the Hematological Malignancies Program at the UCSF Comprehensive Cancer Center. He is currently an HHMI Faculty Scholar, supported by an NCI Outstanding Investigator Award (R35) and serves as mentor for graduate students, clinical and postdoctoral fellows.

Program Name(s)

Translational Research Program

Project Title

Rational repurposing effort to disrupt beta-catenin protein degradation in B-cell malignancies

Mechanisms of tumor-initiation in B-lymphoid malignancies

Memorial Sloan Kettering Cancer Center

I am an MD/PhD physician scientist in the oncology fellowship at MSKCC where I treat leukemia and perform research to understand molecular underpinnings of the disease. My prior work at Brandeis University, Cold Spring Harbor Lab, Harvard Medical School, and Albert Einstein College of Medicine was focused on basic mechanisms of gene expression regulation and I am now studying RNA dysregulation in leukemia. During my PhD, I developed novel methods to study RNA binding proteins in collaboration with Nobel Laureate Dr. Michael Rosbash and Rosenstiel Prize winner Dr. Robert H Singer (my PhD mentor). This integrative approach to studying RNA is ideal for understanding understudied proteins that regulate splicing factor mutations in the Abdel-Wahab lab. For my career, I aim to use novel approaches to understand how the most prevalent splicing factor mutations in blood cancers drive progression and transformation.

Program Name(s)

Career Development Program

Project Title

Targeting SF3B1 splicing factor mutant myeloid malignancies through dependency on GPATCH8

Washington University in St. Louis

Dr. Challen is currently an Associate Professor in the Division of Oncology at Washington University School of Medicine (St. Louis). His laboratory research is at the interface of stem cell biology and blood cancer, and aims to determine how disruption of the epignenome changes the fate of HSCs and ultimately leads to the development of hematopoietic disorders. He was the first to describe how mutations in the gene DNMT3A regulates the balance of HSC self-renewal and differentiation as a first step to development of AML. His lab aims to develop mutation-specific therapies to inhibit CH clones as a mechanism of blood cancer prevention.

Dr. Challen is investigating how mutations in genes that alter the epigenome alter the function of blood-forming hematopoietic stem cells (HSCs), leading to a condition known as clonal hematopoiesis (CH) and predispose for future development of blood diseases such as myelodysplastic syndromes (MDS), acute myeloid leukemia (AML)and T-cell acute lymphoblastic leukemia (T-ALL).

Program Name(s)

Career Development Program

Translational Research Program

Project Title

Synergism of cell-intrinsic and cell-extrinsic factors in the clonal evolution of pre-malignant HSCs

Precision Medicine For DNMT3A-Mutant T-cell ALL

Columbia University Irving Medical Center

My research interests are the identification of genetic alterations responsible for leukemia and lymphoma development and the elucidation of the mechanisms leading to transformation in lymphoid diseases. My academic training and research experience give me an excellent background in multiple biological disciplines including cellular and molecular biology and genetics. I completed my PhD at the INSERM in France where I demonstrated the cooperation between an activating mutation of Jak3 and trisomy 21 in the development of cutaneous T cell lymphoma. I also identified a major cooperative role for the RAS/MAPK signaling pathway in the development of Down syndrome-associated B-cell acute lymphoblastic leukemia. Currently, I am a postdoctoral researcher at Columbia University, under the mentorship of Dr. Teresa Palomero, and I study the mechanisms of transformation in Peripheral T-cell lymphoma using multidisciplinary approaches from animal models to transcriptomic and epigenomic analysis.

Program Name(s)

Career Development Program

Project Title

Role of ID2 in mature T-cell lymphoma

Josep Carreras Leukemia Research Institute

Dr. Melnick is a recognized leader in the fields of hematologic malignancies and cancer epigenetics. Among his major contributions are the first large-scale epigenomic studies in humans, which demonstrated that aberrant epigenetic programming is a hallmark of cancer and that epigenetic diversity is a key determinant of tumor fitness and poor clinical outcomes. These findings led to important mechanistic insights—for example, how mutations in IDH1 and IDH2 disrupt the epigenome through the production of an aberrant oncometabolite, and how mutations in TET2, WT1, IDH1/2, and FLT3 promote leukemogenesis through cooperative epigenetic reprogramming. This was the basis for him receiving the ASH Beutler Award for Outstanding Translational Research in 2020.  Dr. Melnick has played a foundational role in establishing the importance of epigenetic dysfunction in lymphomagenesis, elucidating the mechanistic roles of chromatin modifiers such as EZH2, CREBBP, EP300, KDM1A, KMT2D, HIST1H1, BTG1, ARID1A, TBL1XR1, and TET2. He has also pioneered studies on nuclear topology and its role in regulating the humoral immune response and the malignant transformation of B cells. In the therapeutic arena, Dr. Melnick has developed novel targeted therapies against key lymphoma oncoproteins such as BCL6, SIRT3, and MALT1, and has helped define the rationale for additional targets, including EZH2. Several of these therapeutic approaches have received FDA approval or progressed to phase III clinical trials. He has authored more than 350 scientific publications, held numerous national leadership roles, organized prominent scientific conferences, and devoted extensive effort to mentoring trainees and junior faculty—many of whom now lead distinguished careers in basic and translational research. Dr. Melnick serves on the Board of Directors of both the Blood Cancer United and the Lymphoma Research Foundation. He also has extensive experience initiating and leading multi-center and international research consortia, and is currently the Principal Investigator of several program grants, including two active Blood Cancer United SCOR and RAFL programmatic grants.  He recently took on the position of the Josep Carreras Institute in Barcelona, a unique, free-standing institute focused exclusively on Blood Cancer research, leveraging a diverse and highly accomplished team of cutting-edge basic, translational and clinical scientists. With expertise in many disciplines including epigenetics, immunology, stem cell biology, metabolism, genetics, cell biology and many others, the team integrates artificial intelligence and state-of-the-art preclinical facilities to lead the world in curing Blood Cancers.  The institute is located in Barcelona, which has become one of the top hotspots for biomedicine and biotech in Europe.

Program Name(s)

Research Accelerator for Follicular Lymphoma

Project Title

The ERADICATE follicular lymphoma consortium: accelerating improved outcomes for FL patients

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

University of Minnesota

Helen Parsons, PhD, MPH, is an Associate Professor in the Division of Health Policy and Management at the University of Minnesota School of Public Health. She has expertise in mixed-methods research, employing a combination of clinical registries, administrative data (e.g., Medicare), surveys and focus groups to understand how adoption of new programs and policies influence reimbursement and health outcomes, including the development and use of survey and administrative data to examine longitudinal health and psychosocial outcomes.

Program Name(s)

Equity in Access

Project Title

The Impossible Choice: The Role of Insurance Design on Financial Toxicity and Access to Care for Individuals with Blood Cancer

Stanford University

Dr. Lori Muffly MD MS is an Associate Professor of Medicine at Stanford University in the Division of Blood and Marrow Transplantation and Cellular Therapy. Dr. Muffly is a clinician and clinical investigator whose research includes both health outcomes and clinical trials pertaining to adults with acute leukemia. Her clinical practice serves adults across Northern California with advanced acute leukemias who require hematopoietic cell transplantation and other cellular immunotherapies. She has a specific research interest in improving access to specialty cancer care and reducing health disparities in young adults with acute lymphoblastic leukemia and has published extensively on these topics. She also serves as the PI of multiple investigator-initiated health outcomes studies and clinical trials, including studies evaluating measurable residual disease in adult acute lymphoblastic leukemia, novel chimeric antigen receptor T cell studies for acute leukemia, and she leads a recently established real world consortium investigating outcomes following cellular therapies administered to adults with acute lymphoblastic leukemia. Dr. Muffly has successfully collaborated with Drs. Parsons and Keegan on several previous studies and publications related to adolescent and young adult leukemia and access to cancer care and has delivered numerous national talks on the subject.

Program Name(s)

Equity in Access

Project Title

Towards Equity in Specialized Cancer Care for Adolescents and Young Adults with Newly Diagnosed Acute Lymphoblastic Leukemia

Albert Einstein College of Medicine

Dr. Will has been a group leader at the Albert Einstein College of Medicine since 2016. She obtained her Ph.D. in Cell Biology from the University of Freiburg, Germany and underwent further training in hematology/oncology with Dr. Ulrich Steidl. With a passion for and through the lens of stem cell biology, Britta’s laboratory seeks to discover novel therapeutic options for patients with myeloid malignancies. Current research concentrates on two largely uncharted territories in blood stem cell aging and leukemic stem cell maintenance - iron homeostasis and highly selective autophagy. Dr. Will also serves as co-leader of the Stem Cell and Cancer Biology Program and directs the Cancer Stem Cell Pharmacodynamics Unit at the NCI-designated Montefiore-Einstein Cancer Center. She is the recipient of prestigious young investigator awards, including from the Pershing Square Sohn Cancer Research Alliance, Gilead, AAMDSIF, Feldstein Medical Foundation, and the Leukemia Research Foundation.

Program Name(s)

Career Development Program

Project Title

Therapeutically actionable molecular safeguards in leukemic stem cells

Dana-Farber Cancer Institute

Constantine Mitsiades MD, PhD, is an Assistant Professor at Dana-Farber Cancer Institute (DFCI), Harvard Medical School, an Associate member of the Broad Institute, Cambridge, MA, and holds the "Shawna Ashlee Corman" Investigatorship in Multiple Myeloma at DFCI. His research focuses on understanding the mechanisms through which myeloma and other blood cancers interact with the bone marrow microenvironment and develop resistance to existing or investigational drugs or immune therapies, and how to target therapeutically those resistance mechanisms. His studies established that inhibition of BET bromodomain proteins blocks the critical oncoprotein c-Myc. His research also informed the design of several regimens which are now FDA-approved, represent a standard-of-care for MM treatment, and have become a "backbone" for combination with other novel agents, e.g., monoclonal antibodies. Several of these regimens contributed to the increased overall survival of MM patients in the last decade.

Program Name(s)

Translational Research Program

Project Title

Pharmacological strategies to enhance T- and NK-cell-based therapies in blood cancers