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Original Article

Engagement of Variant CD44 Confers Resistance to Anti-Integrin Antibody-Mediated Apoptosis in a Colon Carcinoma Cell Line

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Pages 21-38 | Received 17 Aug 1997, Accepted 05 Jan 1998, Published online: 11 Jul 2009

References

  • Agrez M.V., et al. Arg-Gly-Asp-containing peptides expose novel collagen receptors on fibroblasts: implications for wound healing. Cell Regul. 1991; 2: 1035–1044
  • Aruffo A.I., et al. CD44 is the principal cell surface receptor for hyaluronate. Cell 1990; 61: 1303–1313
  • Ayroldi E., et al. CD44 (Pgp-1) inhibits CD3 and dexamethasone-induced apoptosis. Blood 1995; 86: 2672–2678
  • Bates R.C., et al. Individual embryonic fibroblasts express multiple β chains in association with the αv integrin subunit. Loss of β3 expression with cell confluence. J. Biol. Chem. 1991; 266: 18593–18599
  • Bates R.C., et al. Apoptosis induced by inhibition of intercellular contact. J. Cell Biol. 1994; 125: 403–415
  • Bates R.C., et al. Involvement of integrins in cell survival. Cancer and Metastasis Reviews 1995; 14: 191–203
  • Boudreau N., et al. Suppression of ICE and apoptosis in mammary epithelial cells by extracellular matrix. Science 1995; 267: 891–893
  • Bourguignon L.Y.W., et al. A CD44-like endothelial cell transmembrane glycoprotein (GPI16) interacts with extracellular matrix and ankyrin. Mol. Cell Bid. 1992; 12: 4464–4471
  • Carter W.G., Wayner E.A. Characterization of the class III collagen receptor, a phosphorylated, transmemhrane glycoprotein expressed in nucleated human cells. J. Biol. Chem. 1988; 263: 4193–4201
  • Davies J., et al. The osteoclast functional antigen, implicated in the regulation of hone resorption, is biochemically related to the vitronectin receptor. J. Cell Biol. 1989; 109: 1817–1826
  • Fearon E.R., Vogelstein B. A genetic model for colorectal carcinogenesis. Cell 1990; 61: 759–767
  • Frisch S.M., Francis H. Disruption of epithelial cell-matrix interactions induces apoptosis. J. Cell Biol. 1994; 124: 619–626
  • Gruber M.F., et al. Stimulation of human monocytes via CD45, CD44 and LFA3 triggers macrophage-colony-stimulating-factor production. Synergism with lipopolysaccharide and IL-beta. J. Immunol. 1992; 148: 1113–1118
  • Gunthert U., et al. A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells. Cell 1991; 65: 13–24
  • Gunthert U., et al. Early detachment of colon carcinoma cells during CD95 (Apol/Fas)-mediated apoptosis. I. De-adhesion from hyaluronate by shedding of CD44. J. Cell Biol. 1996; 134: 1089–1096
  • Hayward I.P., et al. Effect of TGF-β on differentiated organoids of the colon carcinoma cell line LIM 1863. Immunol. Cell Biol. 1995; 13: 249–257
  • Heider K.-H., et al. A human homologue of the rat metastasis-associated variant of CD44 is expressed in colorectal carcinomas and adenomatous polyps. J. Cell Biol. 1993; 120: 227–233
  • Hockenberry D., et al. Bcl-2 is an inner mitochondrial membrane protein that blocks programmed cell death. Nature 1990; 348: 334–336
  • Jalkanen S., Jalkanen M. Lymphocyte CD44 binds the COOH-terminal heparin-binding domain of fibronectin. J. Cell Biol. 1992; 116: 817–825
  • Kalomiris E.L., Bourguignon L.Y.W. Mouse T lymphoma cells contain a transmembrane glycoprotein (gp85) that binds ankyrin. J. Cell Biol. 1988; 99: 1613–1623
  • Kim H., et al. CD44 expression in colorectal adenomas is an early event occurring prior to K-ras and p53 gene mutation. Arch. Biochem. Biophys. 1994; 310: 504–507
  • Kremmidiotis G., et al. Characterization of a monoclonal antibody with CD44 like reactivity. Dis. Markers 1991; 9: 9–20
  • Lacy B.E., Underhill C.B. The hyaluronate receptor is associated with actin filaments. J. Cell Biol. 1987; 105: 1395–1404
  • Lesley J., et al. CD44 and its interaction with extracellular matrix. Adv. Immunol. 1993; 54: 271–335
  • Mackay C.R., et al. Expression and modulation of CD44 variant isoforms in humans. J. Cell Biol. 1994; 124: 71–82
  • Matsumara Y., Tarin D. Significance of CD44 gene products for cancer diagnosis and disease evaluation. Lancet 1992; 340: 1053–1058
  • Meredith J., et al. The extracellular matrix as a cell survival factor. Mol. Biol. Cell 1993; 4: 953–961
  • Montgomery A.M.P., et al. Integrin αvβ3 rescues melanoma cells from apoptosis in three-dimensional dermal collagen. Proc. Natl. Acad. Sci. USA 1994; 91: 8856–8860
  • Nesbitt S. Epitope analysis of the vitronectin receptor (CD51). Leucocyte Typing IV. Oxford University Press, London 1989
  • Noble P.W., et al. Hyaluronate activation of CD44 induces insulin-like growth factor expression by a tumor necrosis factor α dependent mechanism in murine macro-phages. J. Clin. Invest. 1993; 91: 2368–2377
  • Peek M.J., et al. A comparison of fetal and newhorn bovine serum components. Aust. J. Med. Lab. Sci. 1989; 10: 40–41
  • Re F., et al. Inhibition of anchorage-dependent cell spreading triggers apoptosis in cultured human endothelial cells. J. Cell Biol. 1994; 127: 537–546
  • Screaton G.R., et al. Genomic structure of DNA encoding the lymphocyte homing receptor CD44 reveals at least 12 alternatively spliced exons. Proc. Natl. Acad. Sci. USA 1992; 89: 12160–12164
  • Stamenkovic I., et al. The hematopoietic and epithelial forms of CD44 are distinct polypeptides with different adhesion potentials for hyaluronate-hearing cells. EMEO J. 1991; 10: 343–348
  • Sy M.S., et al. Distinct effects of two CD44 isoforms on tumor growth in vivo. J. Exp. Med. 1991; 174: 859–866
  • Underhill C. CD44: The hyaluronan receptor. J. Cell Sci. 1992; 103: 293–298
  • Vaux D.L., et al. Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells. Nature 1988; 335: 440–442
  • Vaux D.L., et al. Prevention of programmed cell death in Caenorhabditis elegans by human Bcl-2. Science 1992; 258: 1955–1957
  • Webb D.S., et al. LFA-3, CD44 and CD45: physiologic triggers of human monocyte TNF and IL-1 release. Science 1990; 249: 1295–1297
  • Whitehead R.H., et al. A new colon carcinoma cell line (LIM 1863) that grows as organoids with spontaneous differentiation into crypt-like structures in vitro. Cancer Research 1987; 47: 2683–2689
  • Wood S. Pathogenesis of metastasis formation observed in vivo in the rabbit ear chamber. Arch. Pathol. 1958; 66: 550–558
  • Zeidman I. The fate of circulating cells. I. Passage of cells through the capillaries. Cancer Research 1961; 21: 38–45
  • Zhang Z., et al. The α5β1 integrin supports survival of cells on fibronectin and up-regulates Bcl-2 expression. Proc. Nail. Acad. Sci. USA 1995; 92: 6161–6165

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