In this Lymphoma Program Project, basic scientists and clinicians will collaborate to study the collection of diseases known as malignant lymphomas. The Program has three major goals: A. THE IMPROVEMENT OF THERAPY FOR PATIENTS WITH HODGKIN'S DISEASE NON- HODGKIN'S LYMPHOMAS We will attempt to improve the cure rate while decreasing the toxicity of current therapy and to develop new modalities of treatment. B. GAINING AN UNDERSTANDING OF THE PATHOGENESIS OF THESE DISEASES Lymphoma tumor cells will be studied using the techniques of molecular biology and immunology. Approaches will be developed to define the nature of host susceptibility, tumor initiation and tumor progression in patients. C. THE STUDY OF NORMAL LYMPHOCYTE BIOLOGY Human lymphoma cells will be used as prototypes of cells at various stages of lymphocyte differentiation. Physiologic processes such as gene activation, recombination and somatic mutation will be investigated. The large numbers of patients who have been and continue to be referred to Stanford represent the major core resource of this program. Clinical trials are conducted on these patients. In addition a large computerized data base has been established which correlates clinical characteristics of these patients and their tumor specimens with outcome of therapy, including long-term complications. These patients serve a source of critical pathologic specimens which are processed, banked and distributed by a Core pathology service to the investigators within this Program Project for a series of important biologic studies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA034233-09
Application #
3093546
Study Section
Special Emphasis Panel (SRC (K1))
Project Start
1986-04-01
Project End
1995-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
9
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Myklebust, June H; Brody, Joshua; Kohrt, Holbrook E et al. (2017) Distinct patterns of B-cell receptor signaling in non-Hodgkin lymphomas identified by single-cell profiling. Blood 129:759-770
Anchang, Benedict; Hart, Tom D P; Bendall, Sean C et al. (2016) Visualization and cellular hierarchy inference of single-cell data using SPADE. Nat Protoc 11:1264-79
Yetil, Alper; Anchang, Benedict; Gouw, Arvin M et al. (2015) p19ARF is a critical mediator of both cellular senescence and an innate immune response associated with MYC inactivation in mouse model of acute leukemia. Oncotarget 6:3563-77
Casey, Stephanie C; Amedei, Amedeo; Aquilano, Katia et al. (2015) Cancer prevention and therapy through the modulation of the tumor microenvironment. Semin Cancer Biol 35 Suppl:S199-S223
Sagiv-Barfi, Idit; Kohrt, Holbrook E; Burckhardt, Laura et al. (2015) Ibrutinib enhances the antitumor immune response induced by intratumoral injection of a TLR9 ligand in mouse lymphoma. Blood 125:2079-86
Behbehani, Gregory K; Samusik, Nikolay; Bjornson, Zach B et al. (2015) Mass Cytometric Functional Profiling of Acute Myeloid Leukemia Defines Cell-Cycle and Immunophenotypic Properties That Correlate with Known Responses to Therapy. Cancer Discov 5:988-1003
Levine, Jacob H; Simonds, Erin F; Bendall, Sean C et al. (2015) Data-Driven Phenotypic Dissection of AML Reveals Progenitor-like Cells that Correlate with Prognosis. Cell 162:184-97
Shroff, Emelyn H; Eberlin, Livia S; Dang, Vanessa M et al. (2015) MYC oncogene overexpression drives renal cell carcinoma in a mouse model through glutamine metabolism. Proc Natl Acad Sci U S A 112:6539-44
Spitzer, Matthew H; Gherardini, Pier Federico; Fragiadakis, Gabriela K et al. (2015) IMMUNOLOGY. An interactive reference framework for modeling a dynamic immune system. Science 349:1259425
Sagiv-Barfi, Idit; Kohrt, Holbrook E K; Czerwinski, Debra K et al. (2015) Therapeutic antitumor immunity by checkpoint blockade is enhanced by ibrutinib, an inhibitor of both BTK and ITK. Proc Natl Acad Sci U S A 112:E966-72

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