Cancer and Metastasis Reviews

, Volume 12, Issue 1, pp 39–52 | Cite as

Autocrine factors, type IV collagenase secretion and prostatic cancer cell invasion

  • Mark E. Stearns
  • Mona Stearns
Article

Summary

Motility factors play a major role in tumor cell invasion and metastases. The biochemical properties of various motility factors; the receptor mediated mechanism of action; the role of microtubules; the potential influence of oncogenes; and the influence of motility factors on type IV collagenase secretion and invasion are discussed. We report on expression of a 70 kDa motility factor, termed invasion stimulating factor (ISF), in human prostatic PC-3 sublines. Boyden chamber chemotactic assays and measurements of type IV collagenase synthesis and secretion suggest that an ISF-receptor dependent mechanism influences tumor cell invasion and protease secretion. Taken together, the evidence that autocrine motility factors play an essential role in tumor cell invasion and metastases is compelling.

Key words

motility factors metastases type IV collagenase prostate cancer 

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References

  1. 1.
    Coman DR: Mechanisms responsible for the origin and distribution of blood-borne tumor metastases. Cancer Res 13: 397–405, 1953Google Scholar
  2. 2.
    Eaves G: The invasiveness growth of malignant tumors as a purely mechanical process. J Pathol 109: 233–237, 1973Google Scholar
  3. 3.
    Strauli P: Proteinases and tumor invasion. In: Strauli P, Barrett AJ, Baici A (eds) Proteinases and Tumor Invasion. Raven Press, New York, 1980, pp 215–222Google Scholar
  4. 4.
    Liotta LA, Thorgeirsson UP, Garbisa S: Role of collagenases in tumor cell invasion. Cancer Mets Rev 1: 277–297, 1982Google Scholar
  5. 5.
    Woolley DE, Tetlow LC, Money CJ, Evanson JM: Human collagenase and its extracellular inhibitors in relation to tumor invasiveness. In: Strand P, Barrett AJ, Baici A (eds) Proteinases and Tumor Invasion. Raven Press, New York, 1980, pp 97–113Google Scholar
  6. 6.
    Liotta LA, Abe S, Gehron P, Martin GR: Preferential digestion of basement membrane collagen by an enzyme derived from a metastatic murine tumor. Proc Natl Acad Sci USA 76: 2268–2276, 1979Google Scholar
  7. 7.
    Nakajima M, Custead SE, Welch DR, Nicolson GL: Type IV collagenolysis: relation to metastatic properties of rat 13762 mammary adenocarcinoma metastatic cell clones. AACR Proceedings 244: 162, 1984Google Scholar
  8. 8.
    Lam WC, Delikatny JE, Orr FW, Wass Jet al.: The chemotactic response of tumor cells: A model for cancer metastasis. Am J Pathol 104: 69–76, 1981Google Scholar
  9. 9.
    McCarthy JB, Basara ML, Palm SL, Sas DF, Furcht LT: Stimulation of haptotaxis and migration of tumor cells by serum spreading factor. Cancer Mets Rev 4: 125–152, 1985Google Scholar
  10. 10.
    Liotta LA, Mandler R, Murano G, Katz DAet al.: Tumor cell autocrine motility factor. Proc Natl Acad Sci USA 83: 3302–3306, 1986Google Scholar
  11. 11.
    Rosen EM, Goldberg ID, Kacinski BM, Buckholtz T, Vinter DW: Smooth muscle releases an epithelial cell scatter factor which binds to heparin. In Vitro Cell Dev Biol 25: 163–173, 1989Google Scholar
  12. 12.
    Yoshida K, Ozaki T, Ushijima K, Hayashi H: Studies on the mechanisms of invasion in cancer. Isolation and purification of a factor chemotactic for cancer cells. Int J Cancer 6: 123–132, 1970Google Scholar
  13. 13.
    Gherardi E, Gray J, Stoker M, Perryman M, Furlong R: Purification of scatter factor, a fibroblast-derived basic protein that modulates epithelial interactions and movement. Proc Natl Acad Sci USA 86: 5844–5848, 1989Google Scholar
  14. 14.
    Rosen E, Meromsky L, Setter E, Vinter DW, Goldberg ID: Quantitation of cytokine-stimulated migration of endothelium and epithelium by a new assay using microcarrier beads. Exp Cell Res 186: 22–31, 1990Google Scholar
  15. 15.
    Rosen EM, Goldberg ID: Protein factors which regulate cell motility. In Vitro Cell Dev Biol 25: 1079–1087, 1989Google Scholar
  16. 16.
    Stoker M, Perryman M: An epithelial scatter factor released by embryo fibroblasts. J Cell Sci 77: 209–223, 1985Google Scholar
  17. 17.
    Stoker M, Gherardi E, Perryman M, Gray J: Scatter factor is a fibroblast-derived modulator of epithelial cell mobility. Nature 327: 239–242, 1987Google Scholar
  18. 18.
    Stracke ML, Guirguis R, Liotta LA, Schiffmann E: Pertussis toxin inhibits stimulated motility independently of the adenylate cyclase pathway in human melanoma cells. Biochem Biophys Res Commun 146: 339–345, 1987Google Scholar
  19. 19.
    Guirguis R, Margulies I, Taraboleth G, Schiffmann E, Liotta LA: Cytokine-induced pseudopodial protrusion is coupled to tumor cell migration. Nature 329: 261–263, 1987Google Scholar
  20. 20.
    Kohn EC, Liotta LA, Schiffmann E: Autocrine motility factor stimulates a three-fold increase in inositol triphosphatase in human melanoma cells. Biochem Biophys Res Commun 166: 757–764, 1990Google Scholar
  21. 21.
    Evans CP, Walsh DS, Kohn EC: An autocrine motility factor secreted by the Dunning R-3327 rat prostatic adenocarcinoma cell subtype AT2.1. Int J Cancer 49: 109–113, 1991Google Scholar
  22. 22.
    Schor SL, Schor AM, Grey AM, Rushton G: Foetal and cancer patient fibroblasts produce an autocrine migrationstimulating factor not made by normal adult cells. Cell Sci 90: 391–399, 1988Google Scholar
  23. 23.
    Grey A-M, Schor AM, Rushton G, Ellis I, Schor S: Purification of the migration stimulating factor produced by fetal and breast cancer patient fibroblasts. Proc Natl Acad Sci USA 86: 2438–2442, 1989Google Scholar
  24. 24.
    Atnip KD, Haney L, Nicolson GL, Dabbous MK: Chemotactic response of rat mammary adenocarcinoma cell clones to tumor-derived cytokines. Biochem Biophys Res Commun 146: 996–1002, 1987Google Scholar
  25. 25.
    Stearns ME, Wang M: Regulation of kinesin expression and type IV collagenase secretion in invasive human prostate PC-3 tumor sublines. Cancer Res 51: 5866–5875, 1991Google Scholar
  26. 26.
    Wang M, Stearns ME: Isolation and characterization of PC-3 human prostatic tumor sublines which preferentially metastasize to select organs in S.C.I.D. mice. Differentiation 48: 115–125, 1991Google Scholar
  27. 27.
    Silletti S, Watanabe H, Timar J, Honn KV, Raz A: Tumor autocrine motility factor: signal transduction and cell growth. Proc Am Assoc Cancer Res 33: 2, 1992Google Scholar
  28. 28.
    Turpeenniemi-Hujanen T, Thorgeirsson UP, Rao CN, Liotta LA: Laminin increases the release of type IV collagenase from malignant cells. J Cell Biochem 261: 1883–1889, 1986Google Scholar
  29. 29.
    Liotta LA, Tryggvason K, Garbisa S, Hart Iet al.: Metastatic potential correlates with enzymatic degradation of basement membrane collagen. Nature (Lond) 284: 67–68, 1980Google Scholar
  30. 30.
    Wang M, Stearns ME: Blocking of collagenase secretion by estramustine duringin vitro tumor cell invasion. Cancer Res 48: 6262–6271, 1988Google Scholar
  31. 31.
    Reich R, Thompson EW, Iwamoto Y, Martin GRet al.: Effects of inhibitor of plasminogen activator, serine proteases and collagenase IV on the invasion of basement membranes by metastatic cells. Cancer Res 48: 3307–3312, 1988Google Scholar
  32. 32.
    Ochieng J, Basolo F, Albini A, Melchiori Het al.: Increased invasive, chemotactic and locomotive abilities of c-Ha-ras-transformed human breast epithelial cells. Invasion Mets 11: 38–47, 1991Google Scholar
  33. 33.
    Seiki M, Sato H, Liotta LA, Schiffmann E: Comparison of autocrine mechanisms promoting motility in two metastatic cell lines: human melanoma and ras-transfected NIH-3T3 cells. Int J Cancer 49: 717–720, 1991Google Scholar
  34. 34.
    Garbisa S, Pozzatti R, Muschel RJ, Saffiotti Uet al.: Secretion of type IV collagenolytic protease and metastatic phenotype. Induction by transfection with c-Ha-ras but not c-Ha-ras plus Ad2-Ela. Cancer Res 47: 1523–1528, 1987Google Scholar
  35. 35.
    Stearns ME, Wang M: Taxol blocks processes essential for prostate tumor cell (PC-3 ML) invasion and metastases. Cancer Res 52: 3776–3781, 1992Google Scholar
  36. 36.
    D'Errico A, Garbisa S, Liotta LA, Castronovo Vet al.: Augmentation of type IV collagenase, laminin receptor, and Ki67 proliferation antigen associated with human colon, gastric, and breast carcinoma progression. Modern Pathol 4: 239–246, 1991Google Scholar
  37. 37.
    Monteagudo C, Merino MJ, San-Juan J, Liotta LA, Stetler-Stevenson WG: Immunohistochemical distribution of type IV collagenase in normal, benign, and malignant breast tissue. Am J Pathol 136: 585–592, 1990Google Scholar
  38. 38.
    Hewitt RE, Leach IH, Powe DG, Clark IMet al.: Distribution of collagenase and tissue inhibitor of metalloproteinases (TIMP) in colorectal tumours. Int J Cancer 49: 666–672, 1991Google Scholar
  39. 39.
    Stearns ME, Wang M: Type IV collagenase (72kDa) expression in human prostate: benign and malignant tissue. Cancer Res 1992, submittedGoogle Scholar
  40. 40.
    Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature (Lond) 227: 680–685, 1970Google Scholar
  41. 41.
    Goldberg GI, Marmer BL, Grant G, Eisen AZet al.: Human 72-kilodalton type IV collagenase forms a complex with a tissue inhibitor of metalloproteinase designated TIMP-2. Proc Natl Acad Sci USA 86: 8207–8211, 1989Google Scholar
  42. 42.
    Nabi IR, Raz A: Cell shape modulation alters glycosylation of a metastatic melanoma cell surface antigen. Int J Cancer 40: 396–401, 1987Google Scholar
  43. 43.
    Nabi IR, Raz A: Loss of metastatic responsiveness to cell shape modulation in a newly characterized B16 melanoma adhesive variant. Cancer Res 48: 1258–1264, 1988Google Scholar
  44. 44.
    Silletti S, Watanabe H, Hogan V, Nabi IR, Raz A: Purification of B16-F1 melanoma autocrine motility factor and its receptor. Cancer Res 51: 3507–3511, 1991Google Scholar
  45. 45.
    Nabi IR, Watanabe H, Silletti S, Raz A: Tumor cell autocrine motility factor receptor. Cell Motility Factors 59: 163–177, 1991Google Scholar
  46. 46.
    Nabi IR, Watanabe H, Raz A: Intracellular localization of a motility factor receptor to tubulovesicles. Cancer Res 50: 409–414, 1990Google Scholar
  47. 47.
    Watanabe H, Carmi P, Hogan V, Raz Tet al.: Purification of human tumor cell autocrine motility factor and molecular cloning of its receptor. J Biol Chem 266: 13442–13448, 1991bGoogle Scholar
  48. 48.
    Watanabe H, Nabi IR, Raz A: The relationship between motility factor receptor internalization and the lung colonization capacity of murine melanoma cells. Cancer Res 1991a, in pressGoogle Scholar
  49. 49.
    Stossel TP: From signal to pseudopod. How cells control cytoplasmic actin assembly. Biol Chem 264: 18261–18264, 1989Google Scholar
  50. 50.
    Liotta L, Schiffmann E: Tumor autocrine motility factors. Cell Motility Factors 59: 17–30, 1991Google Scholar
  51. 51.
    Stoker M, Gherardi E: Regulation of cell movement: the mitogenic cytokines. Biochem Biophys Acta 1072: 81–102, 1991Google Scholar
  52. 52.
    Arakaki N, Hirono S, Ishii T, Kimoto Met al.: Identification and partial characterization of two classes of receptors for human hepatocyte growth factor on adult rat hepatocytes in primary culture. J Biol Chem 267: 7101–7107, 1992Google Scholar
  53. 53.
    Weidner KM, Behrens J, Vandekerchove J, Birchmeier W: Scatter factor: Molecular characteristics and effect on invasiveness of epithelial cells. J Cell Biol 111: 2097–2108, 1990Google Scholar
  54. 54.
    Heldin C-H, Backstrom G, Ostman A, Hammacher Aet al.: Binding of different dimeric forms of PDGF to human fibroblasts: evidence for two different receptor types. Eur Mol Biol Org J 7: 1387–1394, 1988Google Scholar
  55. 55.
    Nister M, Hammacher A, Mellstrom K, Siegbahn Aet al.: A glioma-derived PDGF: A chain homodimer has different functional activities from a PDGF AB heterodimer purified from human platelets. Cell 52: 791–799, 1988Google Scholar
  56. 56.
    Stoker M, Gherardi E: Scatter factor and other regulators of cell motility. Br Med Bull 45: 481–491, 1989Google Scholar
  57. 57.
    Mohler JL, Broskie EN, Ranparia DJ, Sharief Yet al.: Cancer cell motility - inhibitory protein in the Dunning adenocarcinoma model. Cancer Res 52: 2349–2352, 1992Google Scholar
  58. 58.
    Guirguis R, Schiffmann E, Liu B, Birkbeck Det al.: Detection of autocrine motility factor in urine as a marker of bladder cancer. J Natl Cancer Inst 80: 1203–1211, 1988Google Scholar

Copyright information

© Kluwer Academic Publishers 1993

Authors and Affiliations

  • Mark E. Stearns
    • 1
  • Mona Stearns
    • 2
  1. 1.Medical College of PennsylvaniaPhiladelphiaUSA
  2. 2.Department of PathologyMedical College of PennsylvaniaPhiladelphiaUSA

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