Dissemination of T Cell Lymphoma to Target Organs: a Post-Homing Event Implicating ICAM-1 and Matrix Metalloproteinases

References

• Liotta L A, Steeg P S, Stetler-Stevenson W G. Cancer metastasis and angiogenesis: an imbalance of positive and negative regulation. Cell 1991; 64: 327
   PubMed Web of Science ®Google Scholar
• Powell W C, Matrisian L M. roles of matrix metallo-proteinases in tumor progression. Curr. Top, Microbiol. Immunol 1996; 213: 1
   PubMed Web of Science ®Google Scholar
• Opdenakker G, Paemen L, Norga K, Masure S. Proteinase inhibition in invasive cancer therapy: four control levels of matrix degradation. Int. J Cancer 1997; 70: 628
   PubMed Web of Science ®Google Scholar
• Basset P, Okada A, Chenard M P, Kannan R, Stoll I, Anglard P, Bellocq J P, Rio M C. Matrix metalloproteinases as stromal effectors of human carcinoma progression: therapeutic implications. Matrix Biol 1997; 15: 535
   PubMed Web of Science ®Google Scholar
• Lieberman M, Decleve A, Ricciardi-Castagnoli P, Boniver J, Finn O J, Kaplan H S. Establishment, characterization and virus expression of cell lines derived from radiation- and virus-induced lymphomas of C57BL/Ka mice. Int J Cancer 1979; 24: 168
   PubMed Web of Science ®Google Scholar
• Miller R A, Coleman C N, Fawcett H D, Hoppe R T, McDougall I R. Sezary syndrome: a model for migration of T lymphocytes to skin. N Engl J Med. 1980; 303: 89
   PubMed Web of Science ®Google Scholar
• Aoudjit F, Potworowski E F, Pierre Y, St. The metastatic characteristics of murine lymphoma cell lines in vivo are manifested after target organ invasion. Blood 1998; 91: 623
   PubMed Web of Science ®Google Scholar
• Koop S, Schmidt E E, MacDonald I C, Morris V L, Khokha R, Grattan M, Leone J, Chambers A F, Groom A C. Independence of metastatic ability and extravasation: metastatic ras-transformed and control fibroblasts extravasatc equally well. Proc Natl Acad Sci 1996; 93: 11080
   PubMed Web of Science ®Google Scholar
• Chambers A F, MacDonald I C, Schmidt E E, Koop S, Morris V L, Khokha R, Groom A C. Steps in tumor metastasis: new concepts from intravital videomicroscopy. Cancer Metastasis Rev 1995; 14: 279
   PubMed Web of Science ®Google Scholar
• Gosslar U, Jonas P, Luz A, Lifka A, Naor D, Hamann A, Holzmann B. Predominant role of alpha 4-integrins for distinct steps of lymphoma metastasis. Proc Natl Acad Sci 1996; 93: 4821
   PubMed Web of Science ®Google Scholar
• Hangan D, Uniyal S, Morris V L, MacDonald I C, Von Ballestrem C, Chau T, Schmidt E E, Chambers A F, Groom A C, Chan B M. Integrin VLA-2 (α2β1) function in post extravasation movement of human rhabdomyosarcoma RD cells in the liver. Cancer Res 1996; 56: 3142
   PubMed Web of Science ®Google Scholar
• Jonas P, Holzmann B, Jablonski-Westrich D, Hamann A. Dissemination capacity of murine lymphoma cells is not dependent on efficient homing. Int J Cancer 1998; 77: 402
   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
   PubMed Web of Science ®Google Scholar
• Stroeken P J, Van Rijthoven E A, Van der Valk M A, Roos E. Targeted disruption of the betal integrin gene in a lymphoma cell line greatly reduces metastatic capacity. Cancer Res. 1998; 58: 1569
   PubMed Web of Science ®Google Scholar
• Gearing A J, Newman W. Circulating adhesion molecules in disease. Immunol Today. 1993; 14: 506
   PubMedGoogle Scholar
• Terol M J, Lopez-Guillermo A, Bosch F, Villamor N, Cid M C, Rozman C, Campo E, Montserrat E. Expression of the adhesion molecule ICAM-1 in non-Hodgkin's lymphoma: relationship with tumor dissemination and prognostic importance. J Clin Oncol. 1998; 16: 35
   PubMed Web of Science ®Google Scholar
• Dustin M L, Rothlein R, Bhan A K, Dinarello C A, Springer T A. Induction by IL 1 and interferon-gamma: tissue distribution, biochemistry, and function of a natural adherence molecule (ICAM-1). J Immunol. 1986; 137: 245
   PubMed Web of Science ®Google Scholar
• Marlin S D, Springer T A. Purified intercellular adhesion molecule-1 (ICAM-1) is a ligand for lymphocyte function-associated antigen 1 (LFA-1). Cell. 1987; 51: 813
   PubMed Web of Science ®Google Scholar
• Diamond M S, Staunton D E, Marlin S D, Springer T A. Binding of the integrin Mac-1 (CD11b/CD18) to the third immunoglobulin-like domain of ICAM-1 (CD54) and its regulation by glycosylation. Cell 1991; 65: 961
   PubMed Web of Science ®Google Scholar
• Rosenstein Y, Park J K, Hahn W C, Rosen F S, Bierer B E, Burakoff S J. CD43, a molecule defective in Wiskott-Aldrich syndrome, binds ICAM-1. Nature 1991; 354: 233
   PubMed Web of Science ®Google Scholar
• Springer T A. Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm. Cell 1994; 76: 301
   PubMed Web of Science ®Google Scholar
• Bailly P, Tontti E, Hermand P, Cartron J P, Gahmberg C G. The red cell LW blood group protein is an intercellular adhesion molecule which binds to CD11/CD18 leukocyte integrins. Eur J Immunol. 1995; 25: 3316
   PubMed Web of Science ®Google Scholar
• Tian L, Yoshihara Y, Mizuno T, Mori K, Gahmberg C G. The neuronal glycoprotein telencephalin is a cellular ligand for the CD11a/CD18 leukocyte integrin. J Immunol. 1997; 158: 928
   PubMed Web of Science ®Google Scholar
• Roos E. Adhesion molecules in lymphoma metastasis. Cancer Metastasis Rev 1991; 10: 33
   PubMed Web of Science ®Google Scholar
• Roossien F F, De Rijk D, Bikker A, Roos E. Involvement of LFA-1 in lymphoma invasion and metastasis demonstrated with LFA-1-deficient mutants. J Cell Biol 1989; 108: 1979
   PubMed Web of Science ®Google Scholar
• Banks R E, Gearing A J, Hemingway I K, Norfolk D R, Perren T J, Selby P J. Circulating intercellular adhesion molecule-1 (ICAM-1), E-selectin and vascular cell adhesion molecule- (VCAM-1) in human malignancies. Br J Cancer 1993; 68: 122
   PubMed Web of Science ®Google Scholar
• Harning R, Myers C, Merluzzi V J. Monoclonal antibodies to lymphocyte function-associated antigen-1 inhibit invasion of human lymphoma and metastasis of murine lymphoma. Clin Exp Metastasis 1993; 11: 337
   PubMed Web of Science ®Google Scholar
• Zahalka M A, Okon E, Naor D. Blocking lymphoma invasiveness with a monoclonal antibody directed against the beta-chain of the leukocyte adhesion molecule (CD 18). J Immunol 1993; 150: 4466
   PubMed Web of Science ®Google Scholar
• Zahalka M A, Okon E, Gosslar U, Holzmann B, Naor D. Lymph node (but not spleen) invasion by murine lymphoma is both CD44- and hyaluronate-dependent. J Immunol. 1995; 154: 5345
   PubMed Web of Science ®Google Scholar
• Xu H, Gonzalo J A, Pierre Y, St, Williams I R, Kupper T S, Cotran R S, Springer T A, Gutierrez-Ramos J C. Leukocytosis and resistance to septic shock in intercellular adhesion molecule 1-deficient mice. J Exp Med 1994; 180: 95
   PubMed Web of Science ®Google Scholar
• Aoudjit F, Potworowski E F, Springer T A, Pierre Y, St. Protection from lymphoma metastasis in ICAM-1 mutant mice: A post-homing event. J Immunol 1998; 161: 233
   Google Scholar
• Sligh J E, Ballantyne C M, Rish S S, Hawkins H K, Smith C W, Bradley A, Beaudet A L. Inflammatory and immune responses are impaired in mice deficient in intercellular adhesion molecule 1. Proc Natl Acad Sci 1993; 90: 8529
   PubMed Web of Science ®Google Scholar
• King P D, Sandberg E T, Selvakumar A, Fang P, Beaudet A L, Dupont B. Novel isoforms of murine intercellular adhesion molecule-1 generated by alternative RNA splicing. J Immunol 1995; 154: 6080
   PubMed Web of Science ®Google Scholar
• Boise L H, Thompson C B. Hierarchical control of lymphocyte survival. Science 1996; 274: 67
   PubMed Web of Science ®Google Scholar
• Hauzenberger D, Klominek J, Holgersson J, Bergstrom S E, Sundqvist K G. Triggering of motile behavior in T lymphocytes via cross-linking of alpha 4 beta 1 and alpha L beta 2. J Immunol 1997; 158: 76
   PubMed Web of Science ®Google Scholar
• Pyszniak A M, Carpenito C, Takei F. The role of LFA-1 (CD11a/CD18) cytoplasmic domains in binding to intercellular adhesion molecule-1 (CD54) and in postreceptor cell spreading. Exp Cell Res 1997; 233: 78–87
   PubMed Web of Science ®Google Scholar
• Goetzl E J, Banda M J, Leppert D. Matrix metallopro-teinases in immunity. J Immunol. 1996; 156: 1
   PubMed Web of Science ®Google Scholar
• Vachula M, Van Epps D E. In vitro models of lymphocyte transendothelial migration. Invasion Metastasis 1992; 12: 66–81
   PubMedGoogle Scholar
• Stetler-Stevenson M, Mansoor A, Lim M, Fukushima P, Kehrl J, Marti G, Ptaszynski K, Wang J, Stetler-Stevenson W G. Expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in reactive and neoplastic lymphoid cells. Blood 1997; 89: 1708
   PubMed Web of Science ®Google Scholar
• Kossakowska A E, Urbanski S J, Huchcroft S A, Edwards D R. Relationship between the clinical aggressiveness of large cell immunoblastic lymphomas and expression of 92 kDa gelatinase (type IV collagenase) and tissue inhibitor of metalloproteinases-1 (TIMP-1) RNAs. Oncol Res 1992; 4: 233
   PubMed Web of Science ®Google Scholar
• Romanic A M, Madri J A. The induction of 72-kD gelatinase in T cells upon adhesion to endothelial cells is VCAM-1 dependent. J Cell Biol 1994; 125: 1165
   PubMed Web of Science ®Google Scholar
• Aoudjit F, Potworowski E F, Pierre Y, St. Bi-directional induction of matrix metalloproteinase-9 and tissue inhibitor of matrix metalloproteinase-1 during T lymphoma/endothelial cell contact: implication of ICAM-1. J Immunol 1998; 160: 2967–2973
   PubMed Web of Science ®Google Scholar
• Shimizu Y, Van Seventer G A, Horgan K J, Shaw S. Roles of adhesion molecules in T-cell recognition: fundamental similarities between four integrins on resting human T cells (LFA-1, VLA-4, VLA-5, VLA-6) in expression, binding, and costimulation. Immunol Rev 1990; 114: 109, Review
   PubMed Web of Science ®Google Scholar
• Arroyo A G, Sanchez-Mateos P, Campanero M R, Martin-Padura I, Dejana E, Sanchez-Madrid F. Regulation of the VLA integrin-ligand interactions through the beta 1 subunit. J Cell Biol 1992; 117: 659
   PubMed Web of Science ®Google Scholar
• Chang A C, Salomon D R, Wadsworth S, Hong M J, Mojcik C F, Otto S, Shevach E M, Coligan J E. Alpha 3 beta 1 and alpha 6 beta 1 integrins mediate laminin/merosin binding and function as costimulatory molecules for human thymocyte proliferation. J Immunol 1995; 154: 500
   PubMed Web of Science ®Google Scholar
• Wayner E A, Gil S G, Murphy G F, Wilke M S, Carter W G. Epiligrin, a component of epithelial basement membranes, is an adhesive ligand for alpha 3 beta 1 positive T lymphocytes. J Cell Biol 1993; 121: 1141
   PubMed Web of Science ®Google Scholar
• Gospodarowicz D, Greenburg G, Foidart J M, Savion N. The production and localization of laminin in cultured vascular and corneal endothelial cells. J Cell Physiol. 1981; 107: 171
   PubMed Web of Science ®Google Scholar
• Hemler M E, Lobb R R. The leukocyte beta 1 integrins. Curr Opin Hematol. 1995; 2: 61
   PubMedGoogle Scholar
• Gunn M D, Tangemann K, Tam C., Cyster J G, Rosen S D, Williams L T. A chemokine expressed in lymphoid high endothelial venules promotes the adhesion and chemotaxis of naive T lymphocytes. Proc Natl Acad Sci USA 1998; 95: 258–263
   PubMed Web of Science ®Google Scholar
• Johnatty R N, Taub D D, Reeder S P, Turcovski-Corrales S M, Cottam D W, Stephenson T J, Rees R C. Cytokine and chemokine regulation of proMMP-9 and TIMP-1 production by human peripheral blood lymphocytes. J Immunol. Mar 1, 1997; 158(5)2327
   PubMed Web of Science ®Google Scholar
• Lalancette M, Aoudjit F, Potworowski E F, Pierre Y, St. Increased tumorigenicity of lymphoma cells overcomes the resistance of ICAM-1-deficent mice to dissemination of lymphoma cells to target organs. Manuscript in preparation
   Google Scholar
• Tang D G, Honn K V. Adhesion molecules and tumor metastasis: an update. Invasion Metastasis 1994; 14: 109–122
   PubMedGoogle Scholar
• Huang Y W, Baluna R, Vitetta E S. Adhesion molecules as targets for cancer therapy. Histol Histopathol 1997; 2: 467–477
   Google Scholar
• Dolcetti R., Maestro R., Gasparotto D., Rizzo S., Boiocchi M. Adhesion molecule expression does not influence the leukemic behavior of murine T- cell lymphomas. Leukemia 1992; 6: 101S
   PubMed Web of Science ®Google Scholar
• Horstmann W G, Timens W. Lack of adhesion molecules in testicular diffuse centroblastic and immunoblastic B cell lymphomas as a contributory factor in malignant behaviour. Virchows Arch 1996; 429: 83–90
   PubMed Web of Science ®Google Scholar