Adhesion Molecule Expression on B-Cells from Acute and Chronic Lymphoid Leukemias

References

• Springer T. A. Adhesion receptors of the immune system. Nature 1990; 346: 425–434
   PubMed Web of Science ®Google Scholar
• Butcher E. C. Cellular and molecular mechanisms that direct leukocyte traffic. Am. J. Pathol. 1990; 136: 3–11
   PubMed Web of Science ®Google Scholar
• Sher B. T., Bargatze R., Holtzmann B., Gallatin W. M., Matthews D., Wu N., Picker L., Butcher E. C., Weissmann I. L. Homing receptors and metastasis. Adv. Cancer Res. 1988; 51: 361–390
   PubMed Web of Science ®Google Scholar
• Ruoslahti E., Giancotti F. Integrins and tumor cell dissemination. Cancer Cells 1989; 1: 119–126
   PubMed Web of Science ®Google Scholar
• Fidler I. J. Origin and biology of cancer metastasis. Cytometry 1989; 10: 637–680
   Google Scholar
• Rusciano D., Burger M. M. Why do cancer cells metastasize into particular organs?. Bio. Essays 1992; 14: 185–194
   PubMed Web of Science ®Google Scholar
• Albelda S. M. Role of integrins and other cell adhesion molecules in tumor progression and metastasis. Lab. Invest. 1993; 68: 4–17
   PubMed Web of Science ®Google Scholar
• Hunkapiller T., Hood L. Diversity of the immunoglobulin gene superfamily. Adv. Immunol. 1989; 44: 1–63
   PubMed Web of Science ®Google Scholar
• Albelda S. M., Buck C. A. Integrins and other cell adhesion molecules. FASEBJ. 1990; 4: 2868–2880
   PubMed Web of Science ®Google Scholar
• Hynes R. O. Integrins: versatility, modulation and signaling in cell adhesion. Cell 1992; 69: 11–25
   PubMed Web of Science ®Google Scholar
• Varki A. Selectins and the mammalian sialic acid-binding lectins. Current Opin. Cell Biol. 1992; 4: 257–266
   PubMedGoogle Scholar
• Haynes B. F., Liao H. X., Patton K. L. The transmembrane hyaluronate receptor (CD44): multiple functions, multiple forms. Cancer Cells 1991; 3: 347–350
   PubMed Web of Science ®Google Scholar
• Underhill C. CD44: the hyaluronan receptor. J. Cell Sci. 1992; 103: 293–298
   PubMed Web of Science ®Google Scholar
• Lesley J., Hyman R., Kincade P. W. CD44 and its interaction with the extracellular matrix. Adv. Immunol. 1993; 54: 271–335
   PubMed Web of Science ®Google Scholar
• Mackay C. R., Terpe H. J., Stauder R., Marston W. L., Stark H., Gunthert U. Expression and modulation of CD44 variant isoforms in humans. J. Cell Biol. 1994; 124: 71–82
   PubMed Web of Science ®Google Scholar
• Bargatze R. F., Wu N. W., Weissman I. L., Butcher E. C. High endothelial venule binding as predictor of the dissemination of passaged murine lymphomas. J. Exp. Med. 1987; 166: 1125–1131
   PubMed Web of Science ®Google Scholar
• Stauder R., Hamader S., Fasching B., Kemmler G., Thaler J., Huber H. Adhesion to high endothelial venules: a model for dissemination mechanisms in non-Hodgkin lymphomas. Blood 1993; 82: 262–267
   PubMed Web of Science ®Google Scholar
• Turley E. A., Belch A. J., Poppema S., Pilarski L. M. Expression and function of a receptor for hyalu-ronan-mediated motility on normal and malignant B lymphocytes. Blood 1993; 81: 446–453
   PubMed Web of Science ®Google Scholar
• Bradstock K., Makrynicola V., Bianchi A., Byth K. Analysis of the mechanism of adhesion of precursor-B acute lymphoblastic leukemia cells to bone marrow fibroblasts. Blood 1993; 82: 3437–3444
   PubMed Web of Science ®Google Scholar
• Pui C. H., Behm F. G., Crist W. M. Clinical and biologic relevance of immunologic marker studies in childhood acute lymphoblastic leukemia. Blood 1993; 82: 343–362
   PubMed Web of Science ®Google Scholar
• De Rossi G., Zarcone D., Mauro F., Cerruti G., Tenca C., Puccetti A., Mandelli F., Grossi C. E. Adhesion molecule expression on B-cell chronic lymphocytic leukemia cells: malignant cell phenotypes define distinct disease subsets. Blood 1993; 81: 2679–2687
   PubMed Web of Science ®Google Scholar
• Larson R. S., Springer T. A. Structure and function of leukocyte integrins. Immunol. Rev. 1990; 114: 181–217
   PubMed Web of Science ®Google Scholar
• Ruoslahti E. Integrins. J. Clin. Invest. 1991; 87: 1–5
   PubMed Web of Science ®Google Scholar
• Springer T. A., Lasky L. A. Sticky sugars for selectins. Nature 1991; 349: 196–197
   PubMed Web of Science ®Google Scholar
• Boyd A. W., Dunn S. M., Fecondo J. V., Culvenor J. G., Duhrsen U., Burns G. F., Wawryk S. O. Regulation of expression of a human intercellular adhesion molecule (ICAM-1) during lymphohematopoietic differentiation. Blood 1989; 73: 1896–1903
   PubMed Web of Science ®Google Scholar
• Stauder R., Greil R., Schulz T. F., Thaler J., Gattringer C., Radaskiewicz T., Dierich M. P., Huber H. Expression of the leukocyte function-associated antigen 1 and 7F7 antigen, an adhesion molecule related to intercellular adhesion molecule-1 (ICAM-1), in non-Hodgkin lymphomas and leukemias: possible influence on growth pattern and leu-kaemic behaviour. Clin. Exp. Immunol. 1989; 77: 234–238
   PubMed Web of Science ®Google Scholar
• Horst E., Meijer C. J. L.M., Radaskiewicz T., Van Don-gen J. J. M., Pieters R., Figdor C. G., Hooftman A., Pals S. T. Expression of a human homing receptor (CD44) in lymphoid malignancies and related stages of lymphoid development. Leukemia 1990; 4: 383–389
   PubMed Web of Science ®Google Scholar
• Maio M., Pinto A., Carbone A., Zagonel V., Gloghini A., Marotta G., Cirillo D., Colombatti A., Ferrara F., Del Vecchio L., Ferrone S. Differential expression of CD54/intercellular adhesion molecule-1 in myeloid leukemias and lymphoproliferative disorders. Blood 1990; 76: 783–790
   PubMed Web of Science ®Google Scholar
• Archimbaud E., Thomas X., Campos L., Maguad J. P., Dorè J. F., Fiere D. Expression of surface adhesion molecules CD54 (ICAM-1) and CD58 (LFA-3) in adult acute leukemia: relationship with initial characteristics and prognosis. Leukemia 1992; 6: 265–271
   PubMed Web of Science ®Google Scholar
• Kansas G., Dailey M. O. Expression of adhesion structures during B cell development in man. J. Immunol. 1989; 142: 3058–3062
   PubMed Web of Science ®Google Scholar
• Pui C. H., Luo X., Evans W., Martin S., Rugg A., Wilimas J., Crist W. M., Hudson M. Serum intercellular adhesion molecule-1 in childhood malignancy. Blood 1993; 82: 895–898
   PubMed Web of Science ®Google Scholar
• Galandrini R., Albi N., Tripodi G., Zarcone D., Terenzi A., Moretta A., Grossi C. E., Velardi A. Antibodies to CD44 trigger effector functions of human T cell clones. J. Immunol. 1993; 150: 4225–4235
   PubMed Web of Science ®Google Scholar
• Gunthert U., Hofmann M., Rudy W., Reber S., Zoller M., Haussmann I., Matzku S., Wenzel A., Ponta H., Herrlich P. A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells. Cell 1991; 65: 13–24
   PubMed Web of Science ®Google Scholar
• Hofmann M., Rudy W., Zoller M., Tolg C., Ponta H., Herrlich P., Gunthert U. CD44 splice variants confer metastatic behaviour in rats: homologous sequences are expressed in human tumor cell lines. Cancer Res. 1991; 51: 5292–5297
   PubMed Web of Science ®Google Scholar
• Heider K. H., Hofmann M., Hors E., van den Berg F., Ponta H., Herrlich P., Pals S. T. A human homolog of the rat metastasis-associated variant of CD44 is expressed in colorectal carcinomas and adenomatous polyps. J. Cell Biol. 1993; 120: 227–233
   PubMed Web of Science ®Google Scholar
• Koopman G., Heider K. H., Horst E., Adolf G. R., van den Berg F., Ponta H., Herrlich P., Pals S. T. Activated human lymphocytes and aggressive non-Hodgkin lymphomas express a homologue of the rat metastasis-associated variant of CD44. J. Exp. Med. 1993; 177.: 897–904
   PubMed Web of Science ®Google Scholar
• Salles G., Zain M., Jiang W., Boussiotis V. A., Shipp M. A. Alternatively spliced CD44 transcripts in diffuse large-cell lymphomas: characterization and comparison with normal activated B cells and epithelial malignancies. Blood 1993; 82: 3539–3547
   PubMed Web of Science ®Google Scholar
• Grossi C. E., Zarcone D., Tenca C., De Rossi G., Mandelli F. Expression of adhesion molecules in lymphoproliferative disorders. Leukemia 1992; 6(Suppl. 4)35–37
   PubMedGoogle Scholar
• Zarcone D., De Rossi G., Tenca C., Mandelli F., Grossi C. E. Adhesion molecules in lymphoproliferative diseases. Eorum, Trends Exp. Clin. Med. 1993; 3: 4–12
   Google Scholar
• Pals S. T., Horst E., Ossekoppele G. J., Figdor C. G., Scheper R. J., Meijer C. J. L.M. Expression of lymphocyte homing receptor as a mechanism of dissemination in non-Hodgkin's lymphoma. Blood. 1989; 73: 885–888
   PubMed Web of Science ®Google Scholar
• Horst E., Meijer C. J. L.M., Radaskiewicz T., Ossekoppele G. J., van Krieken J. H. J.M., Pals S. T. Adhesion molecules in the prognosis of diffuse large cell lymphoma: expression of a lymphocyte homing receptor (CD44), LFA-I (CDlla/CD18), and ICAM-1 (CD54). Leukemia 1990; 4: 595–599
   PubMed Web of Science ®Google Scholar
• Picker L. J., Medeiros L. J., Weiss L. M., Warnke R. A., Butcher E. C. Expression of lymphocyte homing receptor antigen in non-Hodgkin's lymphoma. Am. J. Pathol. 1988; 130: 496–504
   PubMed Web of Science ®Google Scholar
• Rabinowitz R., Polliack A., Leizerowitz R., Keren-Zwe Y., Schlesinger M. Expression of CDlla(LFA-1) on B-CLL and lymphoma cells: Correlation with cell surface immunoglobulin intensity and CD58 (LFA3). Leukemia and Lymphoma: 5th Int. Workshop on CLL. Advances in CLL, A. Polliack, E. Montserrat. Harwood Acad. Pub. 1991; 59–64
   Google Scholar