Who We Fund

OHSU Knight Cancer Institute

Samantha Tauchmann Ph.D. is a postdoc at the Oregon Health & Science University. She received a B.S. in Molecular Life Sciences from Maastricht University in the Netherlands and her M.Sc. in Biomedical Sciences from the Transnational University Limburg. She completed her PhD under the mentorship of Prof. Dr. Jürg Schwaller at the University Children`s Hospital Basel in Switzerland, where she investigated the role of the methyltransferase NSD1 and the key erythroid transcription factor, GATA1, in erythroleukemia. Dr. Tauchmann joined the Maxson laboratory in February 2023. Her postdoctoral studies are focused on uncovering how SETBP1 mutations contribute to leukemia by modulating the function of methyltransferases. With a strong commitment to understanding blood cell development and leukemia biology, Dr. Tauchmann aspires to identify new therapeutics for SETBP1-mutant leukemias. Her long-term goal is to run an academic laboratory focused on epigenetic dysregulation in blood cancers.

Project Title

Histone methyltransferases as key dependencies in SETBP1-mutant leukemias

The University of Texas MD Anderson Cancer Center

Dr. Issa is a clinical and translational researcher in the Departments of Leukemia and Genomic Medicine at the MD Anderson. His work focuses on the genetic underpinnings of leukemia to uncover therapeutic vulnerabilities, mechanisms of disease progression, and treatment response. Through this research, he aims to develop safe and effective targeted therapies

His clinical research centers on menin inhibitors. He serves as Principal Investigator on numerous investigator-initiated studies and multi-institutional trials, which led to the FDA approval off revumenib for KMT2A-rearranged acute leukemia. He is also a lead investigator or steering committee member for global phase 3 trials evaluating menin inhibition in combination with standard of care for newly diagnosed AML. Dr. Issa leads a precision medicine program for acute leukemias susceptible to menin inhibition, focusing on biomarker discovery, MRD assays, resistance mechanisms, and rational combination therapies.

Program Name(s)

Career Development Program

Project Title

Advancing Precision Medicine through Menin Inhibitors in Acute Leukemia

Emory University

Lawrence Boise, PhD is the R. Randall Rollins Chair of Oncology and Professor in the Department of Hematology and Medical Oncology in the Emory University School of Medicine. Dr. Boise also serves as the Associate Director of Education and Training in the Winship Cancer Institute of Emory University. He received his PhD from VCU-Medicine and did his postdoctoral training at the University of Michigan and the University of Chicago. Dr. Boise took his first faculty position at the University of Miami in 1996 and rose to the rank of Professor before moving to Emory in 2009. Dr. Boise was involved in early studies to identify genes that control cell survival and cell death and has been studying these processes to better understand how to improve our treatment of cancer, particularly the plasma cell malignancy multiple myeloma. Dr. Boise serves as a Senior Editor at Molecular Cancer Research and is on the editorial board of Blood Cancer Discovery.

Program Name(s)

Discovery

Project Title

Functional dissection of heterogeneity of responses to CAR T cells using Spatiotemporal Image-guided Genomic and Cellular Analysis (SaGA) in myeloma

TAP Partner

Constellation Pharmaceuticals was a clinical-stage biopharmaceutical company developing novel therapeutics that selectively modulate gene expression to address serious unmet medical needs in patients with cancer. MorphoSys acquired Constellation in 2021 and then Novartis acquired MorphoSys in 2024. Novartis continues to develop pelabresib in patients with myelofibrosis.

Program Name(s)

Therapy Acceleration Program

Project Title

Development of BET protein bromodomain inhibitors for the treatment of patients with hematologic malignancies

Cincinnati Children's Hospital

Dr. Bailee Kain is from Geneseo, IL and received her B.S. in Biochemistry from University of Missouri in 2016. She completed her doctoral thesis work at Baylor College of Medicine in Dr. Katherine King's laboratory, where she studied how antigenically diverse pathogens reprogram hematopoietic stem cells to induce innate immune cross-protection. In November 2022, Bailee joined Dr. Lee Grimes lab at Cincinnati Children's Hospital Medical Center (CCHMC) as a postdoctoral research fellow. In the Grimes lab, she has focused on determining the oncogenic potential of novel variants found in African Ancestry AML patients, including PHIP. Through nominating PHIP as a functional oncogene, she hopes to combat cancer health disparities by making AML screening, risk stratification, and therapeutic strategies more inclusive. Following her training, Bailee's goal to is to develop an independent research program focused on understanding the disease mechanism of ancestry specific variants found in AML.

Program Name(s)

Career Development Program

Project Title

Functionalizing novel PHIP variants in ancestry-specific acute myeloid leukemia

Yale

Dr. Manyi Wei gained his B.S. degree at China Pharmaceutical University in Nanjing. Subsequently, he completed his Ph.D. training in Cell Biology at the Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences. During his Ph.D. research, Dr. Wei focused on the regulatory role of long non-coding RNA in gene expression and its impact on neuronal function. Dr. Wei has always nurtured a particular interest in understanding and developing novel treatment for leukemia. After his Ph.D. training, Dr. Wei joined the laboratory of Dr. Stephanie Halene at Yale Cancer Center and Yale University School of Medicine. He immediately began exciting work on RNA modifications and their functions in the initiation and progression of acute myeloid leukemia and myelodysplastic syndromes and importantly on novel therapeutic approaches exploiting cell intrinsic and extrinsic effects of targeted inhibitors of RNA methylation. His goal is to contribute to the cure of leukemia.

Program Name(s)

Career Development Program

Project Title

Harnessing METTL3 inhibition in acute megakaryoblastic leukemia driven by the t(1;22) fusion involving a member of the m6A writer complex

Perelman School of Medicine at the University of Pennsylvania

The molecular mechanisms of cell proliferation and the field of Ubiquitin Proteasome System (UPS) have always been our main area of interest and fascination. We have the expertise, training and motivation necessary to study several different aspects of this incredibly broad field. Specifically, the training in mechanistic science, including molecular biology, biochemistry, cell/animal biology, has laid the groundwork to understand how ubiquitin ligases complexes monitor the molecular mechanisms in normal and malignant hematopoiesis. Our work has identified and studied multiple key factors regulating cellular pathways, such as DNA-damage checkpoints, cell cycle, circadian clock, Toll-like-Receptor and NF-κB activation, as documented in ours publications. In addition, we have successfully collaborated with several scientists, and contributed to peer-reviewed publications from each of these projects.

Program Name(s)

Career Development Program

Project Title

Relevance of ubiquitin dependent proteolysis in diffuse large B-cell lymphoma

The University of Texas MD Anderson Cancer Center

Nitin Jain, MD, is an Associate Professor in the Department of Leukemia at MD Anderson Cancer Center in Houston. He earned his medical degree from the All India Institute of Medical Sciences, New Delhi. He completed Internal Medicine residency at the Medical College of Wisconsin and fellowship in Hematology/Oncology at the University of Chicago. Dr. Jain research interests include new drug development for patients with chronic lymphocytic leukemia (CLL) and acute lymphoblastic leukemia (ALL). Dr. Jain is Principal Investigator of several investigator-initiated phase I-II clinical trials, including combination targeted therapies (ibrutinib and venetoclax) in CLL, checkpoint inhibitors in Richter transformation, novel CD22 antibody drug conjugate in B-ALL, venetoclax + chemotherapy in B- and T-ALL, and off-the-self allogeneic CAR-T in B-ALL. The trial combining ibrutinib and venetoclax was published in New England Journal of Medicine in 2019. He has won many awards including ASCO merit award, Sabin Family Foundation Award in 2018 and MD Anderson Faculty Scholar award in 2020.

Program Name(s)

Career Development Program

Translational Research Program

Project Title

Combination Targeted Therapy in Chronic Lymphocytic Leukemia

LCK-targeted Therapy in T cell Acute Lymphoblastic Leukemia

University of Miami

Despite Hodgkin lymphoma’s (HL) favorable prognosis, Black and Hispanic patients have worse survival rates compared to White patients. Insurance status and non-White race and ethnicity are associated with the inequitable receipt of optimal treatments, as well as survivorship care. Patients’ decision-making experiences with their clinicians influence cancer care, and shared decision-making (SDM) is central to patient-centered care when patients have multiple treatment options. However, in hematologic cancer care, many physicians underestimate patient preference for SDM, and HL survivors report minimal involvement in decision-making about their treatment and care.

Program Name(s)

Equity in Access

Project Title

Insurance Inequities in Hodgkin Lymphoma Treatment and Survivorship in the Southeast

Memorial Sloan Kettering Cancer Center

Anita Kumar, MD is an Associate Attending at Memorial Sloan Kettering Cancer Center where she specializes in mantle cell lymphoma. Dr. Kumar leads the Memorial Sloan Kettering mantle cell lymphoma research program. She serves as a principal investigator for a number of clinical trials studying novel therapies for the treatment of mantle cell lymphoma and novel clinical applications of minimal residual disease assessment. She completed her undergraduate studies in Biochemical Sciences at Harvard College and medical school at Northwestern University. She then completed her internship and residency at the Brigham and Women's Hospital and subsequently completed her hematology/oncology fellowship at Memorial Sloan Kettering Cancer Center.

Program Name(s)

Career Development Program

Project Title

Novel Immunotherapy Combinations in Relapsed, Refractory Mantle Cell Lymphoma

Memorial Sloan Kettering Cancer Center

Coming soon.

Program Name(s)

Student Mentorship and Research Training (SMART)

Project Title

Therapeutic potential of mitochondrial transplantation in the treatment of MDS

Dana-Farber Cancer Institute

Dr. Hantel is a faculty member in the Divisions of Population Sciences and Leukemia at DFCI and an Instructor in Medicine at Harvard Medical School. His research focuses on characterizing and remediating clinical trial enrollment disparities for patients with blood cancers, for which he has been awarded career development awards from the NCI (K08) and ASCO to develop and test related multilevel interventions. He also leads multicenter care delivery trials assessing social determinants of health and the impact of Duffy null phenotype on trial participation and outcomes. Work related to these projects has led to multiple publications in journals such as in JAMA, JCO, JNCI, and NEJM. He co-chairs the working group of the DFCI Clinical Trial Access Committee and serves as the Health Disparities and Leukemia Committee Liaison for the Alliance cooperative group. In his clinical role, he cares for patients with leukemia and related hematologic malignancies.

Program Name(s)

Equity in Access

Project Title

The Collaboration and Infrastructure Program for Diversifying Blood Cancer Clinical Trials