The mission of the Hematopoietic Malignancies (HE) Program is to improve the outcome of patients with leukemia, lymphoma, and multiple myeloma through basic and translational laboratory studies and clinical investigation. The HE Program has established a highly interactive transdisciplinary approach that includes efforts directed at: (1) genetic discovery; (2) modeling hematopoietic malignancy-associated genetic lesions; (3) characterizing signal transduction pathways that are crucial for cellular growth control and are perturbed in hematologic cancers; (4) testing experimental therapeutics with molecular analysis to ascertain mechanisms of drug action and drug resistance; (5) defining genetic and environmental risk factors that contribute to the development of hematologic cancers; and (6) translation of these findings into novel therapeutic approaches for leukemia, lymphoma, and multiple myeloma patients. This research is conducted across three unifying themes: Theme 1: Gaining a Greater Understanding of the Molecular Pathogenesis of Hematopoietic Malignancies Theme 2: Undertaking Translational Studies to Identify, Develop, and Optimize Treatment Options for Patients with Hematopoietic Malignancies Theme 3: Advancing Therapeutic Interventions and Understanding Risk Factors to Improve Outcomes in Patients with Hematopoietic Malignancies HE Program: Key Metrics Membership (7 departments, 2 schools) 26 Full 17 Associate 9 Cancer-relevant Funding (direct costs as of $9,433,185 05/31/2017) NCI $2,481,966 26% Peer-reviewed $2,725,651 29% Non-peer-reviewed $4,225,568 45% Cancer-relevant Publications (1/2012-7/2017) 301 Inter-programmatic 79 26% Intra-Programmatic 68 23% High-Impact 139 46% Accruals to Clinical Trials (2016) 134 37 Therapeutic 78 25 Other Interventional 9 1 Non-interventional 47 11

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA082103-21
Application #
9965774
Study Section
Subcommittee H - Clinical Groups (NCI)
Project Start
Project End
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
21
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
Sannino, Sara; Guerriero, Christopher J; Sabnis, Amit J et al. (2018) Compensatory increases of select proteostasis networks after Hsp70 inhibition in cancer cells. J Cell Sci 131:
Lam, Christine; Ferguson, Ian D; Mariano, Margarette C et al. (2018) Repurposing tofacitinib as an anti-myeloma therapeutic to reverse growth-promoting effects of the bone marrow microenvironment. Haematologica 103:1218-1228
Truillet, Charles; Parker, Matthew F L; Huynh, Loc T et al. (2018) Measuring glucocorticoid receptor expression in vivo with PET. Oncotarget 9:20399-20408
Phillips, Kathryn A; Trosman, Julia R; Deverka, Patricia A et al. (2018) Insurance coverage for genomic tests. Science 360:278-279
Phillips, Kathryn A (2018) Evolving Payer Coverage Policies on Genomic Sequencing Tests: Beginning of the End or End of the Beginning? JAMA 319:2379-2380
Puri, Sapna; Roy, Nilotpal; Russ, Holger A et al. (2018) Replication confers ? cell immaturity. Nat Commun 9:485
An, Zhenyi; Aksoy, Ozlem; Zheng, Tina et al. (2018) Epidermal growth factor receptor and EGFRvIII in glioblastoma: signaling pathways and targeted therapies. Oncogene 37:1561-1575
Behr, Spencer C; Villanueva-Meyer, Javier E; Li, Yan et al. (2018) Targeting iron metabolism in high-grade glioma with 68Ga-citrate PET/MR. JCI Insight 3:
Rubenstein, James L; Geng, Huimin; Fraser, Eleanor J et al. (2018) Phase 1 investigation of lenalidomide/rituximab plus outcomes of lenalidomide maintenance in relapsed CNS lymphoma. Blood Adv 2:1595-1607
An, Zhenyi; Knobbe-Thomsen, Christiane B; Wan, Xiaohua et al. (2018) EGFR Cooperates with EGFRvIII to Recruit Macrophages in Glioblastoma. Cancer Res 78:6785-6794

Showing the most recent 10 out of 192 publications