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" Mechanisms in B-Cell Neoplasia 1988 : "
edited by Michael Potter, Fritz Melchers.
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BL
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753272
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b573233
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| Main Entry
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edited by Michael Potter, Fritz Melchers.
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Mechanisms in B-Cell Neoplasia 1988 : : Workshop at the National Cancer Institute, National Institutes of Health, Bethesda, MD, USA, March 23-25, 1988\ edited by Michael Potter, Fritz Melchers.
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| Publication Statement
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Berlin, Heidelberg : Springer Berlin Heidelberg, 1988
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| Series Statement
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Current topics in microbiology and immunology, 141.
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(xiv, 340 pages 122 illustrations)
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| ISBN
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3642740065
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: 9783642740060
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| Contents
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I: Pathogenetic Mechanisms --; Early B Cell Tumors --; B Cell Precursors in Bone Marrow: In Vivo Proliferation, Localization, Stimulation by Activated Macrophages and Implications for Oncogenesis --; Lymphoid-Restricted Stem Cells --; Recombinant Interleukin-7 Supports the Growth of Normal B Lymphocyte Precursors --; Mac-1+ Bone Marrow Cells Include Precursors of B Cells and T Cells --; Molecular Characterization of a Transforming Retrovirus Involved in Pre-B Cell Lymphomas --; In Vitro Transformation of Murine Bone Marrow Cells with a v-raf/v-myc Retrovirus Yields Clonally Related Mature B Cells and Macrophages --; Closely Related BCR/ABL Oncogenes Are Associated with the Distinctive Clinical Biologies of Philadelphia Chromosome Positive Chronic Myelogenous and Acute Lymphocytic Leukemia --; The Pathogenesis of Tumors Induced by Helper Virus-Free Abelson Murine Leukemia Virus --; The Development of Three Distinct Avian B Cell Lymphomas --; Bursal Stem Cells as Targets for myc-Induced Preneoplastic Proliferation and Maturation Arrest --; Molecular Analysis, of an AIDS-Associated Burkitt's Lymphoma: Near-Identity with Endemic Cases --; B Cell and Plasma Cell Tumors --; Transgenic Mouse Models for Hematopoietic Tumorigenesis --; Genetic Studies on Eµ-myc Transgenic Mice --; Differential Expression of myc-family Genes During Development: Normal and Deregulated N-myc Expression in Transgenic Mice --; Plasmacytoma Induction by J Series of v-myc Recombinant Retroviruses: Evidence for the Requirement of Two (raf and myc) Oncogenes for Transformation --; Synergy of an IgH Promoter-Enhancer-Driven c-myc/v-Ha-ras Retrovirus and Pristane in the Induction of Murine Plasmacytomas --; The Genetics of Susceptibility to RIM-Induced Plasmacytomagenesis --; Significance of Chromosome 8 Breakpoint Location in Burkitt's Lymphoma: Correlation with Geographical Origin and Association with Epstein-Barr Virus --; B Cell Proliferation in Follicles, Germinal Centre Formation and the Site of Neoplastic Transformation in Burkitt's Lymphoma --; Altered Growth Phenotype of a Burkitt's Lymphoma Line Following the Introduction and Stable Expression of the EBNA 2A Gene --; Soluble CD23/BLAST-2 (S-CD23/Blast-2) and Its Role in B Cell Proliferation --; Burkitt's Lymphoma Variant Translocations: Distribution of Chromosomal Breakpoints and Perturbated Regulation of a Mutated c-myc Gene --; Differentiation Associated c-myc Expression in Phorbol Ester and Lymphokine Stimulated B-Type Chronic Lymphocytic Leukemia Cells --; B and T Cell Responses Induced by Interleukin-6 --; II: Studies of B Cell Relevant Oncogenes --; c-myc --; Prediction of a Dimerization Surface Common to a New Class of Sequence-Specific DNA Binding Proteins --; Immunological Probes in the Analysis of myc Protein Expression --; The Replication Activity of SV40 DNA Correlates with the Level of c-myc Expression in Human Tumor Cell Lines --; Elevated Levels of the c-myc Protein in Bloom's Syndrome and Induction of c-myc by DNA Strand Breakage --; Deregulation of the c-myc and N-myc Genes in Transformed Cells --; Stimulation of the Antigen Receptor Complex Leads to Transcriptional Activation of the c-myc Gene in Normal Human T Cells --; A Repressor of c-myc Transcription Is Found Specifically in Plasmacytomas --; Regulation of c-myc Gene Transcription in B Lymphocytes: Mechanisms of Negative and Positive Control --; Multifactorial Regulation of the Human c-myc Oncogene --; Negative Control Elements Within and Near the Murine c-myc Gene --; Disruption of the Putative c-myc Auto-Regulation Mechanism in a Human B Cell Line --; Deregulated Expression of an Activated Allele of Human c-myc in Transfected Fibroblast Cultures --; Comparison of c-, N-, and L-myc Transcriptional Regulation --; Delivery of c-myc Antisense Phosphorothioate Oligodeoxynucleotides to Hematopoietic Cells in Culture by Liposome Fusion: Specific Reduction in c-myc Protein Expression Correlates with Inhibition of Cell Growth and DNA Synthesis --; Different Biological Effects of c-myc and H-ras Oncogene Expression in EBV-Infected Human Lymphoblasts --; c-abl --; Abrogation of IL-3 Dependence of Myeloid FDC-P1 Cells by Tyrosine Kinase Oncogenes Is Associated with Induction of c-myc --; U.R. RAPP The Abelson Protein Is Required for Initiation and Maintenance for Transformation in Murine Pre-B Cells --; c-myb --; Expression and Function of the c-myb Oncogene During Hematopoietic Differentiation --; Sense and Anti-sense Transcription in the Murine c-myb Attenuator Region --; bcl-2 --; Expression of the Murine Proto-Oncogene bcl-2 Is Stage Specific and Cell-Type Specific --; Recent Progress on the Human bcl-2 Gene Involved in Follicular Lymphoma: Cheracterization of the Protein Products.
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| Abstract
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The papers in this book were presented at the 6th Workshop on Mechanisms in B-Cell Neoplasia, held in Bethesda, March 23-25, 1988. On alternate years this meeting is sponsored by the . ;. Basel Institute of Immunology in Basel, Switzerland and by the National Cancer Institute in Bethesda, and is attended by 100 to 150 partiƯ cipants. This 6th workshop, like the preceding five, was characterized by intense and enthusiastic discussion which reflects, we think, the exciting growth and development of this field. It is quite clear, however, that despite many general advances an understanding of the precise underlying mechanisms in B-cell tumor development is not yet defined. Probably, there is no single mechanism for all the various forms of B-cell neoƯ plastic development. Many different forms of B-cell neoplasms are known, and these are distinguished by several characteristics: 1) the stage of development attained by the tumor stem cells; 2) mode of growth (slow or fast); 3) association with natural or inductive etiologic agents and 4) specific and consistent mutational mechanisms such as retroviral insertion, chromosomal rearrangement. Those characƯ teristic forms which arise naturally in relatively high frequency or those tumors with hallmark properties which can be induced consistently are the models most frequently studied, e. g., endemic Burkitt's lymphoma, follicular lymphoma, acute and chronic lymphocytic leukemia and mUltiple myeloma in man; bursal lymphoma in chickens; Abelson virus induced pre B cell lymphomas and plasmacytomas in mice and immunocytomas in rats. Each model system, has special problems and advantages.
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Immunology.
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Medicine.
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Oncology.
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| Added Entry
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Fritz Melchers
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Michael Potter
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