Who We Fund

NYU Grossman School of Medicine

My laboratory is committed to transforming lymphoma research into better, more personalized treatments for patients. We study the genetic, epigenetic, metabolic, and microenvironmental factors that drive lymphoma growth and treatment response, with the goal of moving discoveries rapidly from the lab to the clinic. Our research has already helped move new ideas into clinical trials. Our work has helped launch clinical trials, identify biomarkers to guide patient selection, and advance innovative strategies such as epigenetic priming to make chemotherapy, immunotherapy, and targeted therapies more effective. We also contributed key preclinical findings that supported the development of FDA-approved compounds for relapsed/refractory lymphoma. More recently, we developed a new microenvironment-based classification of B-cell lymphoma that has already improved treatment selection and outcomes in clinical trials.

Program Name(s)

Translational Research Program

Project Title

Targeting the microenvironment to increase immunity and immunotherapy response in DLBCL

Children's Research Institute

Michael Keller, M.D., is a pediatric immunologist at Children's National Hospital and specializes in the diagnosis and treatment of primary and secondary immunodeficiency disorders. He has authored many peer-reviewed articles and contributed to expert consensus guidelines on the treatment and diagnosis of primary immunodeficiency disorders. Dr. Keller is a member of the American Academy of Allergy, Asthma, and Immunology (AAAAI); the Clinical Immunology Society; the European Society of Immunodeficiency; and the Primary Immunodeficiency Treatment Consortium (PIDTC).  Dr. Keller's research focuses on the use of adoptive T-cell therapies for treatment of infections in immunocompromised patients, including the use of this therapy to improve outcomes in children with primary immunodeficiency disorders as well as those undergoing bone marrow transplantation for cancer. 

He is the primary investigator of several Phase I-II studies of virus-specific T-cell immunotherapy. Dr. Keller lives in Maryland with his wife and two sons; and enjoys travel, hiking, and martial arts.

Program Name(s)

Translational Research Program

Project Title

T-cell immunotherapy for prevention of COVID-19 following bone marrow transplantation

Northwestern University

I began my scientific career in the Marchesi laboratories (Yale, 1982-1985) and then as an undergraduate under Don Wiley (Harvard, 1986-1988). I entered the Medical Scientist Training Program (1988-1995) at the University of California, San Francisco (UCSF), performing doctoral research with Harold Varmus, at UCSF and the NIH. I defended my thesis at UCSF and completed medical training at Northwestern (1996-1997). I was an Internal Medicine house officer and Hematology/Oncology fellow at Univ of Chicago (UofC, 1997-2003)then stayed on as a UofC faculty member as a physician-scientist, with both research and clinical responsibilities (2003-2023).

Effective April 1, 2023, I have joined the Feinberg School of Medicine at Northwestern University as the inaugural director of the Jeff and Marianne Silver Family Blood Cancer Institute of the Robert H. Lurie Comprehensive Cancer Center. I will also serve as Clinical Director of Cancer Genetics.

I derive synergy between bench research and the bedside to understand disease on a molecular level. This proposal seeks to understand how inherited DNA changes influence the development of bone marrow cancers, with the goal of developing interventions that would prevent cancers in at-risk individuals to make my job as an oncologist obsolete.

Program Name(s)

Discovery

Project Title

CHEK2 as a predisposition gene for clonal hematopoiesis and hematopoietic malignancies

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

Emory University

Dr. Ji is a health services researcher with extensive experience leveraging insurance payer data to study policy issues pertaining to U.S. healthcare systems, with an emphasis on Medicaid. Her research strives to understand the effect of Medicaid policies on healthcare access and outcomes for vulnerable youth and adults. She recently extended this experience to data on pediatric and adolescent/young adult (AYA) cancer survivorship. She co-leads (with Dr. Sharon Castellino) NCI 1R03CA259665-01 to investigate how the Affordable Care Act affects treatment timeliness and survival in AYAs with cancer. She leads a Medicaid initiative within the Childhood Cancer Survivor Study, where she oversees an ongoing linkage of administrative Medicaid data to a nationwide cohort of cancer survivors. She also leads a Junior Faculty Focused Award evaluating Medicaid coverage continuity for pediatric cancer survivors in a single institution.

Program Name(s)

Equity in Access

Project Title

Impact of Health Insurance on Mortality for Children and AYAs Newly Diagnosed with a Blood Cancer: A Population-Based Multistate Evaluation

Houston Methodist Research Institute

I am a translational tumor immunologist. I have 30 years of experience as a well-funded and published researcher and am one of the leading investigators in the fields of tumor immunology in myeloma and other cancers. My laboratory has been working on: (1) characterizing myeloma- and tumor-specific T cells and their subsets and examining their functions, (2) identifying novel myeloma-associated antigens and better methods for immunotherapy, (3) investigating the cross-talk between the tumor microenvironment (TME) and immune system, (4) conducting clinical trials to evaluate the efficacy of immunizing patients with idiotype or dendritic cell-based vaccines, and (5) exploring immunotherapies using myeloma antigens such as DKK1. Our recent research focuses on: (a) developing novel therapeutic mAbs and CAR-T cells for cancers, (b) identifying T-cell subsets that have potent antitumor effects after adoptive transfer, and (c) identifying TME components that induce tumor drug resistance.

Program Name(s)

Translational Research Program

Project Title

Developing Novel CAR-T Cell Therapy For Hematologic Malignancies

Columbia University Medical Center

Dr. Jing Fu is an Assistant Professor of Medical Sciences at Columbia University Vagelos College of Physicians and Surgeons. She earned her PhD in Biochemistry and Molecular Biology from Peking University and completed postdoctoral training at the University of Pittsburgh Cancer Institute. Her research focuses on translational studies of multiple myeloma and AL amyloidosis, with an emphasis on developing novel immunotherapeutic strategies. She investigates the molecular mechanisms underlying disease progression, immune evasion, bone disease, and therapeutic resistance to identify new therapeutic targets and advance precision immunotherapy for patients with plasma cell disorders.

Program Name(s)

Translational Research Program

Project Title

Targeting GCK as a novel and selective therapeutic strategy against RAS mutated Multiple Myeloma

Dana-Farber Cancer Institute

Dr. Mark Murakami is a physician-scientist dedicated to advancing curative treatments for follicular lymphoma. Based in the Division of Hematologic Neoplasia at the Dana-Farber Cancer Institute, Dr. Murakami leads a research group focused on understanding how minute numbers of lymphoma cells survive the initial effect of treatment, persist even when patients are in clinical remission, and later expand to cause relapse. Eradication of these rare cells, called minimal residual disease, is felt to be the key to curing follicular lymphoma. Dr. Murakami has dedicated his career to developing methods for tracking, isolating, and analyzing minimal residual disease and understanding how these cells evade pharmacologic therapy as well as the anti-lymphoma immune response. He uses this information to devise novel treatments for rigorous evaluation – first in the laboratory and eventually in clinical trials run by clinical colleagues – that we hope will cure follicular lymphoma.

Program Name(s)

Translational Research Program

Project Title

Exploiting tumor-immune dynamics to inform curative combination therapy for follicular lymphoma

Massachusetts General Hospital

Subha was born and raised in India where he completed his Masters in Biochemistry from the University of Calcutta, India. Thereafter, he joined the Ph.D. program at Institute of Life Sciences, to pursue a career in research. His past research work focused on the role of chromatin remodelling complexes in guiding differentiation  programs and lineage choices in hematopoiesis, and how these epigenetic switches can contribute to leukemic transformation. Presently, he is a postdoctoral fellow in Dr. Peter Miller's lab at Massachusetts General Hospital and Harvard Medical School.  Menin inhibitors (MIs), have recently emerged as an exciting new modality for treating AML. However, MIs are not curative and associated with toxicities like differentiation syndrome. His overachieving goal here is to dissect mechanisms of MIs and come up with combination strategies/targets that can improve the efficacy of MIs in order to achieve profound and long lasting responses in AML patients.

Program Name(s)

Career Development Program

Project Title

Leveraging p53 to Improve Menin Inhibition in Leukemia Therapy

MD Anderson Cancer Center

Dr. DiNardo is an academic clinical researcher with a primary focus on individualized therapy and precision oncology for myeloid malignancies, including the optimal incorporation of genomics into standard risk assessments and treatment algorithms, and the clinical evaluation of targeted therapeutics for molecularly-defined patient subgroups.

Program Name(s)

Career Development Program

Project Title

A precision-based all-oral combination of venetoclax, oral decitabine, and IDH1/2 targeted inhibition for patients with IDH1 or IDH2 mutated AML

Cincinnati Children’s Hospital Medical Center

I am an Assistant Professor at Cincinnati Children's Hospital Medical Center. My areas of research interest include drug development and signaling with focus on small GTPases. My research is both basic and translational.

My research efforts encompass several methodologies, including structural biology, biophysical and biochemical studies, cellular functional assays, and ultimately, identifying small molecule compounds that bind to and modulate GTPase signaling in in vivo pre-clinical models of cancer.

RAC GTPases are key regulators of cell growth. By reorganizing the actin cytoskeleton, RAC plays a key role in cancer cell metastasis. It is also involved in mechanisms of resistance to therapies. My lab's goal is to inhibit RAC in leukemia by understanding the molecular mechanisms driving its hyperactivity.

One of my lab’s groundbreaking discoveries is the identification of a small molecule inhibitor of VAV3, a RAC activator. Current research studies the efficacy of VAV3 inhibition in models of relapsed/recurrent leukemia.

Program Name(s)

Translational Research Program

Project Title

Overcoming RAS-driven Mechanisms of Resistance in Leukemia

Winship Cancer Institute

Dr. Jean Koff is an Associate Professor in the Department of Hematology and Medical Oncology and Director of the Lymphoma Program’s Translational Research Team at Winship Cancer Institute of Emory University. Her clinical expertise in lymphoma is complemented by her research characterizing the immunologic and genetic factors that contribute to poor outcomes in lymphoma patient populations under-represented in most studies, such as African Americans and organ transplant recipients. She serves as an investigator on several team science projects involving multi-institutional cohorts of lymphoma patients with integrated analyses of clinical and molecular data, including the Lymphoma Epidemiology of Outcomes cohort study. Dr. Koff is the 2024 Chair of the Scientific Committee on Lymphoid Neoplasia for the American Society of Hematology. Her work has been funded by the Lymphoma Research Foundation, the American Association for Cancer Research, the American Cancer Society, and the NIH.

Program Name(s)

Specialized Center of Research Program

Project Title

Translating molecular profiles into treatment approaches to target disparities in lymphoma