The long-term goal of this project remains an understanding of the mechanisms that promote transformation and progression of B cell lymphomas. To this end, we have focused, and will continue to focus on avian Lymphoid Leukosis (LL) as a model system. Like other lymphomagenic systems, the natural history of LL has been characterized as a multistage process of transformation that involves pre-neoplastic, neoplastic and metastaic stages; however the basis for progression from one stage to the next is poorly understood. We will take advantage of expertise recently developed in our laboratory to isolate individual hyperplastic follicles that will now permit analysis of cells at all three stages of LL tumor development. We propose to analyze factors intrinsic to the B cell that are likely to be integral to the transformation process, i.e., provival composition, orientation and site of integration, and single or multiple proto-oncogene activation, to determine their role in the transformation and progression of the LL tumors. We will also examine the relationship between the state of cellular differentiation/maturation, and the susceptibility of B cells to transformation and the potential of transformed B cells to metastasize. Finally, we will analyse the effects of the selective pressures caused by immune mechanisms on the progression of cells at each stage of lymphomagenesis. These experiments should provide insight into the mechanisms of neoplastic transformation and tumor progression as well as the processes of normal B cell development and thereby a context for the interpretation of the neoplastic changes.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA039000-06
Application #
3177609
Study Section
Experimental Immunology Study Section (EI)
Project Start
1986-09-30
Project End
1992-08-31
Budget Start
1990-09-01
Budget End
1992-08-31
Support Year
6
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Wistar Institute
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Press, R D; Reddy, E P; Ewert, D L (1994) Overexpression of C-terminally but not N-terminally truncated Myb induces fibrosarcomas: a novel nonhematopoietic target cell for the myb oncogene. Mol Cell Biol 14:2278-90
Olson, W C; Ewert, D L (1994) A novel multilineage cell-surface antigen expressed on terminally differentiated chicken B cells in mucosal tissues. Cell Immunol 154:328-41
Fynan, E F; Ewert, D L; Block, T M (1993) Latency and reactivation of Marek's disease virus in B lymphocytes transformed by avian leukosis virus. J Gen Virol 74 ( Pt 10):2163-70
Givol, I; Greenhouse, J J; Hughes, S H et al. (1992) Retroviruses that express different ras mutants cause different types of tumors in chickens. Oncogene 7:141-6
Eguchi, Y; Ewert, D L; Tsujimoto, Y (1992) Isolation and characterization of the chicken bcl-2 gene: expression in a variety of tissues including lymphoid and neuronal organs in adult and embryo. Nucleic Acids Res 20:4187-92
Fynan, E; Block, T M; DuHadaway, J et al. (1992) Persistence of Marek's disease virus in a subpopulation of B cells that is transformed by avian leukosis virus, but not in normal bursal B cells. J Virol 66:5860-6
England, J M; Panella, M J; Ewert, D L et al. (1991) Induction of a diffuse mesothelioma in chickens by intraperitoneal inoculation of v-src DNA. Virology 182:423-9
Zhang, J Y; Olson, W; Ewert, D et al. (1991) The v-rel oncogene of avian reticuloendotheliosis virus transforms immature and mature lymphoid cells of the B cell lineage in vitro. Virology 183:457-66
Barth, C F; Ewert, D L; Olson, W C et al. (1990) Reticuloendotheliosis virus REV-T(REV-A)-induced neoplasia: development of tumors within the T-lymphoid and myeloid lineages. J Virol 64:6054-62
Ewert, D L; Steiner, I; DuHadaway, J (1990) In ovo infection with the avian retrovirus RAV-1 leads to persistent infection of the central nervous system. Lab Invest 62:156-62

Showing the most recent 10 out of 17 publications