The Differing Types of Tumor Cell Invasion: Invasion of Elastic Lamina

References

• Dedhar S. Integrins and tumor invasion. Bio Essays 1990; 12: 583–590
   PubMed Web of Science ®Google Scholar
• Cossman J, Schlegal R. The diagnosis of human neoplasia. J Natl Cancer Inst 1991; 83: 980–981
   PubMed Web of Science ®Google Scholar
• Parsons D F. Near-diploid tumor cell lines for cancer research. Cancer Cells 1989; 1: 96–98
   PubMed Web of Science ®Google Scholar
• Parsons D F, Marko M, Braun S J. Ascites tumor invasion of mouse peritoneum studied by high-voltage electron microscope stereoscopy. Cancer Res 1982; 42: 4574–4583
   PubMed Web of Science ®Google Scholar
• Parsons D F, Marko M., Wansor K J. Inflammation with restricted lysosomal proteolysis during early ascites carcinoma invasion of mouse parietal peritoneum. A medium and high-voltage electron microscopic and cytochemical study. Tissue Cell 1983; 15: 499–507
   PubMed Web of Science ®Google Scholar
• Parsons D F, Marko M, Radermacher M. Shape changes and polarization of cells migrating through tissue. A high-voltage electron microscope and computer graphics study of serial sections. Tissue Cell 1985; 17: 491–510
   PubMed Web of Science ®Google Scholar
• Parsons D F, Marko M, Leith A. Organelle rearrangement and cell volume changes during “squeezing invasion” of peritoneal elastic lamina by targeted murine breast carcinoma cells. Tissue Cell 1991; 23: 293–305
   PubMed Web of Science ®Google Scholar
• Parsons D F, Foley J, Marko M. Immediate ascites conversion of mammary tumors induced in NYLR/Nya mice by 7, 12-dimethylbenz-[a] anthracene and urethane feeding and by forced breeding. Cancer Invest 1986; 4: 109–126
   PubMed Web of Science ®Google Scholar
• Parsons D F, Marko M, Sacks P G. Targeting of peritoneum by the small numbers of isogeneic and allogeneic ascites carcinoma cells that infiltrate or attach to peritoneum during ascites growth. Cancer Invest 1990; 8: 483–491
   PubMed Web of Science ®Google Scholar
• Terranova V P, Liotta L A, Russo R G. Role of laminin in the attachment and metastasis of murine tumor cells. Cancer Res 1982; 42: 2265–2269
   PubMed Web of Science ®Google Scholar
• Terranova V P, Hujanen E S, Loeb D M. Use of a reconstituted basement membrane to measure cell invasiveness and select for highly invasive tumor cells. Proc Natl Acad Sci USA 1986; 83: 465–469
   PubMed Web of Science ®Google Scholar
• McCarthy J B, Palm S L, Furcht L T. Migration by haptotaxis of a Schwann cell tumor line to the basement membrane plycoprotein laminin. J Cell Biol 1983; 97: 772–777
   PubMed Web of Science ®Google Scholar
• Noel A C, Calle A, Emonard H P. Invasion of reconstituted basement membrane matrix is not correlated to the malignant metastatic cell phenotype. Cancer Res 1991; 51: 405–414
   PubMed Web of Science ®Google Scholar
• Talbot I C, Ritchie S, Leighton M, Hughes A O. Invasion of veins by carcinoma of the rectum: Method of detection, his-tological features and significance. Histopathology 1981; 5: 141–163
   PubMed Web of Science ®Google Scholar
• Tamura S, Enjoji M. Elastosis in neoplastic and nonneoplastic tissues from patients with mammary carcinoma. Acta Pathol Jpn 1988; 38: 1537–1546
   PubMedGoogle Scholar
• Kagan H M, Vaccaro C A, Bronson R E. Ultrastructural im-munolocalization of lysyl oxidase in vascular connective tissue. J Cell Biol 1986; 103: 1121–1128
   PubMed Web of Science ®Google Scholar
• Richmond V L. Elastin and elastin-associated-protein of porcine aorta and lung. Connect Tiss Res 1990; 25: 131–137
   PubMed Web of Science ®Google Scholar
• Baccarani-Contri M, Vincenzi D, Cicchetti F. Immuno-cytochemical localization of proteoglycans within normal elastin fibers. Eur J Cell Biol 1990; 53: 305–312
   PubMed Web of Science ®Google Scholar
• Gibson M A, Kumaratilake J S, Cleary E G. The protein components of the 12-nanometer microfibrils of elastic and non-elastic tissues. J Biol Chem 1989; 264: 4590–4598
   PubMed Web of Science ®Google Scholar
• Gibson M A, Sandberg L B, Grosso L E. Complementary DNA cloning establishes microfibril-associated glycoprotein (MAGP) to be a discrete component of the elastin-associated microfibrils. J Bid Chem 1991; 266: 7596–7601
   PubMed Web of Science ®Google Scholar
• Streeten B W, Gibson S A. Identification of extractabk proteins from the bovine ocular zonule: Major zonular antigens of 32 kD and 250 kD. Current Eye Res 1988; 7: 139–146
   PubMed Web of Science ®Google Scholar
• Grosso L E, Park P W, Mecham R P. Characterization of a putative clone for the 67-kDa elastin/laminin receptor suggests that it encodes a cytoplasmic protein rather than a cell surface receptor. Biochemistry 1991; 30: 3346–3350
   PubMed Web of Science ®Google Scholar
• Mecham R P, Hinek A, Griffin G L. The elastin receptor shows structural and functional similarities to the 67-kDa tumor cell laminin receptor. J Biol Chem 1989; 264: 16652–16657
   PubMed Web of Science ®Google Scholar
• Mecham R P, Whitehouse L, Hay M. Ligand affinity of the 67-kD elastin/laminin binding protein is modulated by the protein's lectin domain: Visualization of elastin/laminin-receptor complexes with gold-tagged ligands. J Cell Biol 1991; 113: 187–194
   PubMed Web of Science ®Google Scholar
• Mecham R P. Laminin receptors. Annu Rev Cell Biol 1991; 7: 71–92
   PubMedGoogle Scholar
• Timar J, Lapis K, Fulop T. Interaction Between elastin and tumor cell lines with different metastatic potential: In vitro and in vivo studies. J Cancer Res Clin Oncol 1991; 117: 232–238
   PubMed Web of Science ®Google Scholar
• Senior R M, Griffin G L, Mechum R P. Chemotactic activity of elastin-derived peptides. Clin Invest 1980; 66: 859–862
   Google Scholar
• Netland P A, Zetter B R. Melanoma cell adhesion to defined extracellular matrix components. Biochem Biophys Res Commun 1986; 139: 1515–522
   Google Scholar
• Tobias J W, Bern M M, Netland P A. Monocyte adhesion to subendothelial components. Blood 1987; 69: 1265–1268
   PubMed Web of Science ®Google Scholar
• DePasquale J A, Izzard C S. Accumulation of talin in nodes at the edge of lamellopodium and separate incorporation into adhesion plaques at focal contacts in fibroblasts. J Cell Biol 1991; 113: 1351–1357
   PubMed Web of Science ®Google Scholar
• Burridge K, Fath K, Kelly T. Focal adhesions: Transmem-brane junctions between the extracellular matrix and the cyto-skeleton. Annu Rev Cell Biol 1988; 4: 487–525
   PubMedGoogle Scholar
• Akiyama S K, Nagata K, Yamada K M. Cell surface receptors for extracellular matrix proteins. Biochim Biophys Acta 1990; 1031: 91–100
   PubMed Web of Science ®Google Scholar
• Yamada K M, Kennedy D W, Yamada S S. Monoclonal antibody and synthetic peptide inhibitors of human tumor cell migration. Cancer Res 1990; 50: 4485–4496
   PubMed Web of Science ®Google Scholar
• Savagner P, Imhof B A, Yamada K M. Homing of hemo-poietic precursor cells to the embryonic thymus: Characterization of the invasive mechanism induced by chemotatic peptides. J Cell Biol 1986; 103: 2715–2727
   PubMed Web of Science ®Google Scholar
• Gehlsen K R, Argraves W S, Pierschbacher M D. Inhibition of in vitro tumor cell invasion by Arg-Gly-Asp-containing synthetic peptides. J Cell Biol 1988; 106: 925–930
   PubMed Web of Science ®Google Scholar
• Mueller S C, Chen W-T. Cellular invasion into matrix beads: Localization of beta I integrins and fibronectin to thc invado-podia. J Cell Sci 1991; 99: 213–225
   PubMed Web of Science ®Google Scholar
• Humphries M J, Olden K, Yamada K M. A synthetic peptide from fibronectin that inhibits experimental metastasis of niurinc melanoma cells. Science 1986; 233: 467–470
   PubMed Web of Science ®Google Scholar
• Guirguis R, Margulies I, Taraboletti G. Cytokinc-induced pseudopodial protrusion is coupled to tumour cell migration. Nature 1987; 329: 261–263
   PubMed Web of Science ®Google Scholar
• Kramer R H, McDonald K A, Crowley E. Melanoma cell adhesion to basement membrane mediated by integrin-related complexes. Cancer Res 1989; 49: 393–402
   PubMed Web of Science ®Google Scholar
• Albini A, Lwamoto Y, Kleinman H K. A rapid in vitro assay for quantitating the invasive potential of tumor cells. Cancer Res 1987; 47: 3239–3245
   PubMed Web of Science ®Google Scholar
• Saiki I, Murata J, Watanabe K. Inhibition of tumor cell invasion by Ubenimex (Bestatin) in vitro. Jpn J Cancer Res 1989; 801: 873–878
   Google Scholar
• Kucich U, Christner P, Lippman M. Utilization of a per-oxidase antiperoxidase complex in an enzyme-linked imniuno-sorbent assay of elasti-derived peptides in human plasma. Am Rev Respir Dis 1983; 131: 709–713
   Google Scholar
• Groult V, Hornebeck W, Ferrari P. Mechanisms of interaction between human skin fibroblasts and elastin: Differences between elastin fibres and derived peptides. Cell Biochem Function 1991; 9: 171–182
   PubMed Web of Science ®Google Scholar
• Hauschka T S, Weiss L, Holdridge B A. Karyotypic and surface features of murine TA3 carcinoma cells during immunoselection in mice and rats. J Natl Cancer lnst 1971; 47: 343–359
   PubMed Web of Science ®Google Scholar