Who We Fund

University of Virginia

I am a trained clinical hematopathologist and physician-scientist who is well versed in both basic and translational studies in hematologic tumors, with a special interest and emphasis in B-cell malignancies: the genetic and epigenetic mechanisms of tumor microenvironment (TME)-induced survival and drug resistance. My long-term goal is to characterize the pathobiology of B-cell lymphomas, especially aggressive B-cell malignancies, and the evolution of resistance to drugs and, more recently, immunotherapy.

Over the last decade, I have developed an active and unique research program for drug screening, chemical proteomics profiling, bulk and scRNAseq, ChIP-seq, ATAC, scATAC, functional pharmacogenomic computational biology, and multiplex immune profiling, and applied it to cell line and primary lymphoma samples to determine the major intrinsic and TME extrinsic molecular determinants governing lymphoma cell response and resistance. By capitalizing a “” opportunity and approach, my long-term goal is to provide major advances in our understanding of the lymphoma biology, develop innovative therapies and exert an immediate favorable impact on treatment for lymphoma patients.

My extensive background in cancer biology and clinical hematology/oncology, with my expertise in novel lymphoma therapies and therapy resistance, make me well-suited to serve as a Principal Investigator on many projects.

Program Name(s)

Mantle Cell Lymphoma Research Initiative

Project Title

Understanding Resistance Mechanism to Enhance CAR-T Immunotherapy for MCL

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 Wisconsin at Madison

I have been interested in basic and translational work related to cancer since my master’s resulting in a thesis on bone metastasis of breast cancer. Part of my PhD work explored the molecular mechanisms of chronic myelogenous leukemia (CML). I have studied the use of metformin, as an anti-cancer agent and demonstrated that metformin through activation of AMPK/ RUNX1/ SOCS3 axis and inhibition of glycolytic fluxes overcomes the imatinib resistance in CML patients. I joined Dr. Jing Zhang’s lab at the University of Wisconsin. Under her guidance, I had a chance to explore the molecular players involved in a subset of acute myeloid leukemia (AML) with concurrent RAS and ASXL1 mutations, which define one of the worst AML prognosis groups. I have been actively collaborating with numerous investigators on and off campus to work on patient derived xenograft model for pre-clinical development of therapeutic approaches targeting both leukemia cells and suppressed T cells in NRAS; ASXL1 AML.

Project Title

Enhancing the cytotoxicity of T cells in NRAS; ASXL1-AML through combined inhibition of MEK and HDACs

MD Anderson Cancer Center

Michael Wang, MD, is Professor of Lymphoma and Myeloma at MD Anderson Cancer Center where he established the Mantle Cell Lymphoma Program of Excellence, the world’s only program dedicated exclusively to MCL research and treatment. He led trials resulting in 3 FDA approvals for MCL treatment. He leads a large lab focusing on overcoming resistance to MCL therapies and developing new ones. His detailed studies of tissue from patients with MCL has been instrumental in setting the stage for this application. Jia Zhou, PhD, is Professor of Pharmacology and Toxicology at the University of Texas Medical Branch. Apart from academia, he worked in the pharmaceutical industry for 7 years. His primary research interest is drug discovery and the development of novel small-molecule therapeutics for cancers and other diseases. He has established a fruitful collaboration with Dr. Wang and his lab and has great experience in leading both the chemical and pharmacological aspects of drug development.

Program Name(s)

Mantle Cell Lymphoma Research Initiative

Project Title

Development of novel BTK-MALT1 dual inhibitors to treat MCL

Duke University Medical Center

Fahmin Basher, MD, PhD completed her bachelor’s degrees in chemical engineering and biological sciences at the University of South Carolina. She then went on to pursue a combined MD/PhD in cancer immunology at the Medical University of South Carolina in the Medical Scientist Training Program under the mentorship of Jennifer Wu, PhD. She completed her internal medicine residency training at the University of Miami prior to transitioning to Duke University for her hematology/medical oncology fellowship training. During her fellowship, she served as chief fellow and was supported by the Duke Hematology and Transfusion Medicine T32 training grant. Her clinical and research interests include a focus in translational immunology, particularly the treatment of hematologic malignancies and optimization of therapeutic approaches and complications after stem cell transplantation and cellular therapy. She is currently being mentored by Stefanie Sarantopoulos, MD, PhD.

Program Name(s)

Career Development Program

Project Title

The Role of the DNA Sensor AIM2 in B Cell Fate and Function After HCT

Washington University in St. Louis

Dr. Tyler Parsons completed his PhD research at Oakland University and the Beaumont Research Institute in the lab of Dr. Gerard Madlambayan where he published on the role of blood stem cells in tumor response to radiation therapy. During the final year of his PhD, he was diagnosed with a myeloproliferative neoplasm (MPN) which directed his career focus and passion to furthering the understanding of MPNs and their transformation potential to leukemia. To this end, he joined the lab of Dr. Grant Challen at Washington University School of Medicine (St. Louis) where he is investigating clonal evolution in MPNs and the mutational trajectory leading to secondary leukemia. The aim of his post-doctoral fellowship is to describe the clonal architecture of MPN disease progression to leukemia which could lead to early detection and improved disease surveillance. He is passionate about improving outcomes for patients by advancing our understanding of both the biology and disease evolution of MPNs.

Program Name(s)

Career Development Program

Project Title

Mechanisms of Clonal Evolution in the Transformation of MPN to sAML

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

University of Fribourg

Nicola Vannini after his MSc degree in Biological Sciences obtained at the University of Parma, moved to La Jolla (CA) where he worked for two years at the Burnham Institute in the laboratory of Prof. John C. Reed studying the metabolic basis of cardiac aging. He completed his PhD at the National Institute for Cancer Research in Genova (Italy) under the supervision of Prof. Adriana Albini, where he worked on nutritional interventions to prevent tumor progression. After his PhD he moved to EPFL (Lausanne, Switzerland) in the laboratory directed by Prof. Matthias Lütolf and Prof. Olaia Naveiras at the EPFL, where he developed targeted metabolic interventions to boost hematopoietic recovery.

Since March 2016 Nicola Vannini is group leader at the Ludwig Cancer Institute at the University of Lausanne . His primary research goals are the understanding of metabolic changes occurring during aging in the hematopoietic and immune compartments and their impact on cancer immunotherapy.

Program Name(s)

Translational Research Program

Project Title

Mitochondrial reprogramming to restore age-driven dysfunction in T cell and boost CAR-T cell therapy

BC Cancer

Dr. Manabu Fujisawa received M.D. from Kyushu University in Fukuoka, Japan. Motivated by the experience as a hematologist having treated many patient with treatment-resistant disease, Dr. Fujisawa conducted a clinical study on clonality and clinical progression in multiple myeloma in Kameda Medical Center, Chiba. Dr. Fujisawa then began his basic research at University of Tsukuba in 2016, where he received PhD under the supervision of Pr. Mamiko Sakata-yanagimoto. Pr. Sakata’s lab focused on clonal hematopoiesis and malignant lymphoma, which Dr. Fujisawa studied the function of clonal hematopoietic-derived immune cells in the tumor microenvironment. In 2022, Dr. Fujisawa joined the laboratory of Pr. Christian Steidl in Lymphoid Cancer Research at the BC Cancer Research Centre in Vancouver, Canada, as a postdoctoral fellow.

Program Name(s)

Career Development Program

Project Title

Spatial architecture and malignant cell characterization of nodular lymphocyte-predominant Hodgkin lymphoma

The Ohio State University

I am a tenured Professor in the Division of Hematology at The Ohio State University, with a focus on translational research in Chronic Lymphocytic Leukemia, the Associate Director for Clinical Research within the Division of Hematology, the Section Head for the CLL/Hairy cell leukemia group, and the co-leader of the Leukemia Research Program within the OSUCCC. I am the PI for multiple early-stage clinical trials investigating novel targeted therapies for CLL and other hematologic malignancies, chaired the intergroup Phase III study A041202 which investigated chemoimmunotherapy versus targeted therapy as initial therapy for older adults with CLL, and now chair A041702 which is investigating continuous versus intermittent targeted therapy in the same patient population. My laboratory research focuses on resistance to targeted therapies in CLL. Our group identified C481S and PLCG2 mutations as the primary resistance mechanisms for covalent BTK inhibitors and were the first to investigate reversible BTK inhibitors preclinically as a strategy to circumvent BTK inhibitor resistance.

Program Name(s)

Translational Research Program

Project Title

Inhibition of PKCβ as a strategy for BTK inhibitor refractory CLL

Perelman School of Medicine at the University of Pennsylvania

Dr. Liling Wan is an Assistant Professor at the University of Pennsylvania. She received a B.S. in Biological Sciences and Biotechnology from Tsinghua University and a Ph.D. in Molecular Biology from Princeton University. She conducted postdoctoral research at Rockefeller University where she studied chromatin regulators in cancer. The Wan lab studies basic gene regulatory mechanisms and how these mechanisms are dysregulated in cancer, with the goal of harnessing these insights for therapeutics. Her research has revealed how chromatin “reader” proteins impact gene regulation in cancer such as acute myeloid leukemia and led to early drug development efforts targeting these mechanisms. Dr. Wan has been recognized for her innovative and impactful research through numerous awards including AACR NextGen Star, NIH Pathway to Independence Award, the NIH Director’s New Innovator Award, and was recently named a Pew-Stewart Scholar, V Foundation Scholar, and ASH Scholar.

Program Name(s)

Career Development Program

Project Title

Epigenetic Mechanisms in Acute Myeloid Leukemia

The University of Texas MD Anderson Cancer Center

Koichi Takahashi, MD, PhD is Associate Professor in the Departments of Leukemia and Genomic Medicine at The University of Texas MD Anderson Cancer Center. He received MD degree from Niigata University School of Medicine and PhD degree from Kyoto University School of Medicine, both in Japan. He then did internal medicine residency at Toranomon Hospital, Tokyo, Japan, and Beth Israel Medical Center in New York, followed by hematology and oncology fellowship at MD Anderson Cancer Center in Houston. During the fellowship, he was trained in Dr. Andrew Futreal’s Lab for cancer genomics. He is board certified in Internal Medicine, Hematology, and Medical Oncology. Dr. Takahashi is well known for his research in delineating how selection of pre-existing clonal hematopoiesis under chemotherapy contributes to the development of therapy-related myeloid neoplasms. His laboratory uses state-of-the-art single-cell technologies to understand the mechanism of leukemia development and create strategies for early detection and prevention.

Program Name(s)

Career Development Program

Project Title

Understanding the clonal origin, evolution, and progression of myeloid malignancies