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Mechanisms of invasion by head and neck cancers

  • Chapter
Head and Neck Cancer

Part of the book series: Cancer Treatment and Research ((CTAR,volume 74))

Abstract

Local and regional spread of squamous cell carcinoma (SCC) of the upper aerodigestive tract represents a major challenge to the oncologist, since it carries a high risk of regional recurrence and a high mortality rate. The invasiveness of these tumors frequently requires surgical resections that impair important physiological functions, including speech and swallowing. The therapy of SCC may be approaching a plateau, as the efficacy and toxicity of the agents used for treatment, particularly chemotherapy, seems to be optimal given present knowledge; therefore, understanding the mechanisms that underlie the invasiveness of SCC is required to develop novel treatments that attenuate the local spread of these tumors. Such anti-invasive agents would not be used alone, but rather in conjunction with existing therapies to improve the overall therapy of head and neck SCC.

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References

  1. Tryggvason K, Höyhtÿa M, Salo T. Proteolytic degradation of extracellular matrix in tumor invasion. Biochim Biophys Acta 907:191–217, 1987.

    PubMed  CAS  Google Scholar 

  2. Nicolson GL, Cancer metastasis: Organ colonization and the cell surface properties of malignant cells. Biochim Biophys Acta 695:113–176, 1982.

    PubMed  CAS  Google Scholar 

  3. Danø K, Andreasen PA, Grøndahl-Hansen J, Kristensen P, Nielsen LS. Plasminogen activators, tissue degradation, and cancer. Adv Cancer Res 44:139–266, 1985.

    Article  PubMed  Google Scholar 

  4. Nakajima M, Irimura T, Nicolson GL, Basement membrane degradative enzymes and tumor metastasis. Cancer Bull 39:142–149, 1987.

    Google Scholar 

  5. Nakajima M, Irimura T, Nicolson GL, Heparanases and tumor metastasis. J Cell Biochem 36:157–167, 1988.

    Article  PubMed  CAS  Google Scholar 

  6. Liotta LA, Rao CN, Wewer UM, Biochemical interactions of tumor cells with the basement membrane. Annu Rev Biochem 55:1037–1057, 1986.

    Article  PubMed  CAS  Google Scholar 

  7. Mignatti P, Robbins E, Rifkin DB. Tumor invasion through the human amniotic membrane: Requirement for a proteinase cascade. Cell 47:487–498, 1986.

    Article  PubMed  CAS  Google Scholar 

  8. Markus G, Takita H, Camiolo SM, Corasanti JG, Evers JL, Hobika GH. Content and characterization of plasminogen activators in human lung tumors and normal lung tissue. Cancer Res 40:841–848, 1980.

    PubMed  CAS  Google Scholar 

  9. Carlsen SA, Ramshaw IA, Warrington RC. Involvement of plasminogen activator production with tumor metastasis in a rat model. Cancer Res 44:3012–3016, 1984.

    PubMed  CAS  Google Scholar 

  10. Clavel C, Chavanel G, Birembaut P. Detection of the plasmin system in human mammary pathology using immunofluorescence. Cancer Res 46:5743–5747, 1986.

    PubMed  CAS  Google Scholar 

  11. Starkey JR. Cell-matrix interactions during tumor invasion. Cancer Metastasis Rev 9: 113–123, 1990.

    Article  PubMed  CAS  Google Scholar 

  12. Duffy MJ. Do proteases play a role in cancer invasion and metastasis? Eur J Cancer Clin Oncol 23:583–589, 1987.

    Article  PubMed  CAS  Google Scholar 

  13. Biswas C. Tumor cell stimulation of collagenase production by fibroblasts. Biochem Biophys Res Commun 109:1026–1032, 1982.

    Article  PubMed  CAS  Google Scholar 

  14. Dabbous MK, North SM, Haney L, Nicolson GL. Macrophage and lymphocyte potentiation of syngeneic tumor cell and host fibroblast collagenolytic activity in rats. Cancer Res 48:6832–6836, 1988.

    PubMed  CAS  Google Scholar 

  15. Dabbous MK, Wooley DE, Haney L, Carter LM, Nicolson GL. Host-mediated effectors of tumor invasion: Role of mast cells in matrix degradation. Clin Exp Metastasis 4:141–152, 1986.

    Article  PubMed  CAS  Google Scholar 

  16. Baici A, Knöpfel M, Keist R. Tumor-host interaction in rabbit V2 carcinoma: Stimulation of cathepsin B in host fibroblasts by a tumor-drived cytokine. Invasion Metastasis 8: 143–158, 1988.

    PubMed  CAS  Google Scholar 

  17. Ossowski L, Reich E. Antibodies to plasminogen activator inhibit human tumor metastasis. Cell 35:611–619, 1983.

    Article  PubMed  CAS  Google Scholar 

  18. Tanaka N, Ogawa H, Tanaka K, Kinjo M, Kohga S. Effects of tranexamic acid and urokinase on hematogenous metastases of Lewis lung carcinoma in mice. Invasion Metastasis 1:149–157, 1981.

    PubMed  CAS  Google Scholar 

  19. Pauli BU, Schwartz DE, Thonar EJM, Kuettner KE. Tumor invasion and host extracellular matrix. Cancer Metastasis Rev 2:129–152, 1983.

    Article  PubMed  CAS  Google Scholar 

  20. Persky B, Ostrowski LE, Pagast P, Ahsan A, Schultz RM. Inhibition of proteolytic enzymes in the in vitro amnion model for basement membrane invasion. Cancer Res 46:4129–4134, 1986.

    PubMed  CAS  Google Scholar 

  21. Yagel S, Warner AH, Nellans HN, Lala PK, Waghorne C, Denhardt DT. Suppression by cathepsin L inhibitors of the invasion of amnion membranes by murine cancer cells. Cancer Res 49:3553–3557, 1989.

    PubMed  CAS  Google Scholar 

  22. Irimura T, Nakajima M, Nicolson GL. Chemically modified heparins as inhibitors of heparan sulfate specific endo-ß-glucoronidase (heparanse) or metastatic melanoma cells. Biochemistry 25:5322–5328, 1986.

    Article  PubMed  CAS  Google Scholar 

  23. Khokha R, Denhardt D. Matrix metalloproteinases and tissue inhibitor of metallopro-teinases: Review of their role in tumorigenesis and tissue invasion. Invasion Metastasis 9:391–405, 1989.

    PubMed  CAS  Google Scholar 

  24. Liotta LA, Steeg PS, Stetler-Stevenson WG. Cancer metastasis and angiogenesis: An imbalance of positive and negative regulation. Cell 64:327–336, 1991.

    Article  PubMed  CAS  Google Scholar 

  25. Hicks NJ, Ward RV, Reynolds JJ. Fibrosarcoma model derived from mouse embryo cells: Growth properties and secretion of collagenase and metalloproteinase inhibitor (TIMP) by tumour lines. Int J Cancer 33:835–844, 1984.

    Article  PubMed  CAS  Google Scholar 

  26. Schultz RM, Silberman S, Persky B, Bajkowski AS, Carmichael DF. Inhibition by human recombinant tissue inhibitor of metalloproteinases of human amnion invasion and lung colonization by murine B16-F10 melanoma cells. Cancer Res 48:5539–5545, 1988.

    PubMed  CAS  Google Scholar 

  27. Khokha R, Waterhouse P, Yagel S, Denhardt D. Antisense RNA-induced reduction in murine TIMP levels confers oncogenicity on Swiss 3T3 cells. Science 243:947–950, 1989.

    Article  PubMed  CAS  Google Scholar 

  28. Verde P, Boast S, Franze A, Robbiati F, Blasi F. An upstream enhancer and a negative element in the 5’ flanking region of the human urokinase plasminogen activator gene. Nucleic Acids Res 16:10699–10715, 1988.

    Article  PubMed  CAS  Google Scholar 

  29. Nielsen L, Hansen J, Skriver L, Wilson E, Kaltoft K, Zenthen J, Danø K. Purification of zymogen to plasminogen activator from human glioblastoma cells by affinity chromatography with monoclonal antibody. Biochemistry 21:6410–6415, 1982.

    Article  PubMed  CAS  Google Scholar 

  30. Collen D, Verstraete M. Molecular biology of human plasminogen. II. Metabolism in physiological and some pathological conditions in man. Thrombosis Diathesis Haemor-rhagica 34:403, 1975.

    CAS  Google Scholar 

  31. Robbins KC, Summaria L, Hsieh B, Shah R. The peptide chains of human plasmin. J Biol Chem 242:2333–2342, 1967.

    PubMed  CAS  Google Scholar 

  32. Liotta L, Goldfarb R, Brundage R, Siegel G, Terranova V, Garbisa, S. Effect of plasminogen activator (urokinase), plasmin, and thrombin on glycoprotein and collagenous components of basement membrane. Cancer Res 41:4629–4636, 1981.

    PubMed  CAS  Google Scholar 

  33. Matrisian L, Bowden T. Stromelysin/transin and tumor progression. Semin Cancer Biol 1:107–115, 1990.

    PubMed  CAS  Google Scholar 

  34. Mackay AR, Corbitt RH, Hartzler JL, Thorgeirsson UP. Basement membrane type IV collagen degradation: Evidence for the involvement of a proteolytic cascade independent of metalloproteinases. Cancer Res 50:5997–6001, 1990.

    PubMed  CAS  Google Scholar 

  35. Markus G, Takita H, Camiola S, Corasanti J, Evers J, Hobika G. Content and characterization of plasminogen activators in human lung tumors and normal lung tissue. Cancer Res 40:841–848, 1980.

    PubMed  CAS  Google Scholar 

  36. Markus G, Camiolo SM, Kohga S, Madeja JM, Mittelman A. Plasminogen activator secretion of human tumors in short-term organ culture, including a comparison of primary and metastatic colon tumors. Cancer Res 43:5517–5525, 1983.

    PubMed  CAS  Google Scholar 

  37. Skriver L, Larsson LI, Kielberg V, Nielsen LS, Andreasen PB, Kristensen P, Danø K. Immunocytochemical localization of urokinase-type plasminogen activator in Lewis lung carcinoma. J Cell Biol 99:752–757, 1984.

    Article  Google Scholar 

  38. Hearing V, Law L, Corti A, Appella E, Blasi F. Modulation of metastatic potential by cell surface urokinase of murine melanoma cells. Cancer Res 48:1270–1278, 1988.

    PubMed  CAS  Google Scholar 

  39. Sappino A, Busso N, Belin D, Vassalli J. Increase of urokinase-type plasminogen activator gene expression in human lung and breast carcinomas. Cancer Res 47:4043–4046, 1987.

    PubMed  CAS  Google Scholar 

  40. Lund L, Ronne E, Roldan A, Behrendt N, Romer J, Blasi F, Danø K. Urokinase receptor mRNA level and gene transcription are strongly and rapidly increased by phorbol myristate acetate in human monocyte-like U937 cells. J Biol Chem 266:5177–5181, 1991.

    PubMed  CAS  Google Scholar 

  41. Hekman CM, Loskutoff DJ. Endothelial cells produce a latent inhibitor of plasminogen activators that can be activated by denaturants. J Biol Chem 260:11581–11587, 1985.

    PubMed  CAS  Google Scholar 

  42. Maddox WA, Urist MM. Histopathological prognostic factors of certain primary oral cavity cancers. Oncology 4:39–42, 1990.

    PubMed  CAS  Google Scholar 

  43. Clayman G, Wang SW, Nicolson GL, El-Naggar A, Mazar A, Henkin J, Balsi F, Goepfert H, Boyd DD. Regulation of urokinase-type plasminogen activator expression in squamous cell carcinoma of the oral cavity. Int J Cancer 54:73–80, 1993.

    Article  PubMed  CAS  Google Scholar 

  44. Niedbala M, Sartorelli AC. Plasminogen activator-mediated degradation of subendothelial extracellular matrix by human squamous carcinoma cell lines. Cancer Commun 2:189–199, 1990.

    PubMed  CAS  Google Scholar 

  45. Wilhelm SM, Collier IE, Marmer BL, Eisen AZ, Grant G, Goldberg G. SV40-transformed human lung fibroblasts secrete a 92-kDa type IV collagenase which is identical to that secreted by normal human macrophages. J Biol Chem 264:17213–17221, 1989.

    PubMed  CAS  Google Scholar 

  46. Bejarano PA, Noekken ME, Suzuki K, Hudson BG, Nagase H. Degradation of basement membranes by human matrix metalloproteinase 3 (stromelysin). Biochem J 256:413–419, 1988.

    PubMed  CAS  Google Scholar 

  47. Matrisian LM. Metalloproteinases and their inhibitors in matrix remodeling. Trends Genet 6:121–125, 1990.

    Article  PubMed  CAS  Google Scholar 

  48. Bernhard EJ, Muschel RJ, Hughes EN. Mr 92,000 gelatinase release correlates with the metastatic phenotype in transformed rat embryo cells. Cancer Res 50:3872–3877, 1990.

    PubMed  CAS  Google Scholar 

  49. Ura H, Bonfil RD, Reich R, Pfeifer A, Harris CC. Expression of type IV collagenase and procollagen genes and its correlation with the tumorigenic, invasive, and metastatic abilities of oncogene-tranformed human bronchial epithelial cells. Cancer Res 49:4615–4621, 1989.

    PubMed  CAS  Google Scholar 

  50. Garbisa S, Pozzatti R, Mushcel RJ, Saffiotti U, Ballin M, Goldfarb R, Khoury G, Liotta L. Secretion of type IV collagenase protease and metastatic phenotype: Induction by trans-fection with c-Ha-ras but not c-Ha-ras plus Ad2-Ela. Cancer Res 47:1523–1528, 1987.

    PubMed  CAS  Google Scholar 

  51. Nakajima M, Welch DR, Belloni PN, Nicolson GL. Degradation of basement membrane type IV collagen and lung subendothelial matrix by rat mammary adenocarcinoma cell clones of differing metastatic potentials. Cancer Res 47:4869–4876, 1987.

    PubMed  CAS  Google Scholar 

  52. DeClerck Y, Perez N, Shimada H, Boone T, Langley K, Taylor S. Inhibition of invasion and metastasis in cells transfected with an inhibitor of metalloproteinases. Cancer Res 52:701–708, 1992.

    PubMed  CAS  Google Scholar 

  53. Schultz RM, Silberman S, Persky B, Bajkoski AS, Carmichael DF. Inhibition by human recombinant tissue inhibitor of metalloproteinases of human amnion invasion and lung colonization by murine B16-F10 melanoma cells. Cancer Res 48:5539–5545, 1988.

    PubMed  CAS  Google Scholar 

  54. Khokha R, Waterhouse P, Yagel S, Lala P, Overall C, Norton G, Denhardt D. Antisense RNA-induced reduction in murine TIMP levels confers oncogenicity on Swiss 3T3 cells. Science 243:947–950, 1989.

    Article  PubMed  CAS  Google Scholar 

  55. Kusukawa J, Sasaguri Y, Shima I, Kameyama T, Morimatsu M. Production of matrix metalloproteinase 2 (gelatinase/type IV collagenase) and 3 (stromelysin) by cultured oral squamous cell carcinoma. J Oral Pathol Med 21:221–224, 1992.

    Article  PubMed  CAS  Google Scholar 

  56. Muller D, Breathnach R, Engelmann A, Millon R, Bronner G, Flesch H, Dumont P, Eber M, Abecassis J. Expression of collagenase-related metalloproteinase genes in human lung or head and neck tumours. Int J Cancer 48:550–556, 1991.

    Article  PubMed  CAS  Google Scholar 

  57. Polette M, Clavel C, Muller D, Abecassis J, Binninger I, Birembaut P. Detection of mRNA encoding collagenase I and stromelysin 2 in carcinomas of the head and neck by in situ hybridization. Invasion Metastasis 11:76–83, 1991.

    PubMed  CAS  Google Scholar 

  58. Kudlow JE, Bjorge JD. TGF-α in normal physiology. Semin Cancer Biol 1:293–302, 1990.

    PubMed  CAS  Google Scholar 

  59. Presta M, Tiberio L, Rusnati M, Dell’era P, Ragnotti G. Basic fibroblast growth factor requires a long-lasting activation of protein kinase C to induce cell proliferation in transformed fetal bovine aortic endothelial cells. Cell Regul 2:719–726, 1991.

    PubMed  CAS  Google Scholar 

  60. Tiefenbrun N, Kimichi A. The involvement of protein kinase C in mediating growth suppressive signals of interferons in hematopoietic cells. Oncogene 6:1001–1007, 1991.

    PubMed  CAS  Google Scholar 

  61. Schutze S, Machleidt T, Kronke M. Mechanisms of tumor necrosis factor action. Semin Oncol 19:16–24, 1992.

    PubMed  CAS  Google Scholar 

  62. Murphy P, Hart D. Modulation of plasminogen activator and plasminogen activator inhibitor expression in the human U373 glioblastoma/astrocytoma cell line by inflammatory mediators. Exp Cell Res 198:93–100, 1992.

    Article  PubMed  CAS  Google Scholar 

  63. Presta M, Maier A, Rusnati M, Moscatelli D, Ragnotti G. Modulation of plasminogen activator activity in human endometrial adenocarcinoma cells by basic fibroblast growth factor and transforming growth factor ß. Cancer Res 48:6384–6389, 1988.

    PubMed  CAS  Google Scholar 

  64. Collart M, Belin D, Vassalli J, Kossodo S, Vassalli P. Gamma interferon enhances macrophage transcription of the tumor necrosis factor/cachetin, interleukin 1, and urokinase genes, which are controlled by short-lived repressors. J Exp Med 164:2113–2118, 1986.

    Article  PubMed  CAS  Google Scholar 

  65. Tienari J, Alanko T, Lehtonen E, Saksela O. The expression and localization of urokinase-type plasminogen activator and its type-1 inhibitor are regulated by retinoic acid and fibroblast growth factor in human teratocarcinoma cells. Cell Regul 2:285–297, 1991.

    PubMed  CAS  Google Scholar 

  66. Okada Y, Tsuchiya H, Shimizu H, Tomita K, Nakanishi I, Sato H, Seike M, Yamashita K, Hayakawa T. Induction and stimulation of 92-kDa gelatinase/type IV collagenase production in osteosarcoma and fibrsarcoma cell lines by tumor necrosis factor a. Biochem Biophys Res Commun 171:610–617, 1990.

    Article  PubMed  CAS  Google Scholar 

  67. Salo T, Lyons JG, Rahemtulla F, Birkedal-Hansen H, Larjava H. Transforming growth factor-ß up-regulates type IV collagenase expression in cultured human keratinocytes. J Biol Chem 266:11436–11441, 1991.

    PubMed  CAS  Google Scholar 

  68. Unemori EN, Hibbs MS, Amento EP. Constitutive expression of a 92-kD gelatinase (type IV collagenase) by rheumatoid synovial fibroblasts and its induction in normal human fibroblasts by inflammatory cytokines. J Clin Invest 88:1656–1662, 1991.

    Article  PubMed  CAS  Google Scholar 

  69. Turksen K, Choi Y, Fuchs E. Transforming growth factor alpha induces collagen degradation and cell migration in differentiating human epidermal raft cultures. Cell Regul 2: 613–625, 1991.

    PubMed  CAS  Google Scholar 

  70. Somers K, Cartwright SL, Schechter GL. Amplification of the int-2 gene in human head and neck squamous cell carcinomas. Oncogene 5:915–920, 1990.

    PubMed  CAS  Google Scholar 

  71. Santini J, Formento J, Francouai M, Milano G, Schneider M, Dassonville O, Demard F. Characterization, quantification, and potential clinical value of the epidermal growth factor receptor in head and neck squamous cell carcinomas. Head Neck 13:132–139, 1991.

    Article  PubMed  CAS  Google Scholar 

  72. Hart IR. Mechanisms of tumor cell invasion. Cancer Biol Rev 2:29–58, 1981.

    Google Scholar 

  73. Mareel MMK. Invasion in vitro: Methods of analysis. Cancer Metastasis Rev 2:201–218, 1983.

    Article  PubMed  CAS  Google Scholar 

  74. Nicolson GL, Poste G. Tumor cell diversity and host responses in cancer metastasis. I. Properties of metastatic cells. Curr Prob Cancer 7:1–83, 1982.

    Article  CAS  Google Scholar 

  75. Varani J. Chemotaxis of metastatic cells. Cancer Metastasis Rev 1:17–28, 1982.

    Article  PubMed  CAS  Google Scholar 

  76. Orr FW, Varani J, Delikatny J, Jain N, Ward PA. Comparison of the chemotactic responsiveness of two fibrosarcoma subpopulations of differing malignancy. Am J Pathol 102:160–167, 1981.

    PubMed  CAS  Google Scholar 

  77. Lacovara J, Cramer EB, Quigley JP. Fibronectin enhancement of directed migration of B16 melanoma cells. Cancer Res 44:1657–1663, 1984.

    PubMed  CAS  Google Scholar 

  78. Graff J, Iwamoto Y, Sasaki M, Martin GM, Kleinman HK, Robey FA, Yamada Y. Identification of an amino acid sequence in laminin mediating cell attachment, chemotaxis, and receptor binding. Cell 48:989–996, 1987.

    Article  Google Scholar 

  79. Wever UM, Taraboletti G, Sobel ME, Albrechtsen R, Liotta LA. Role of laminin in tumor cell migration. Cancer Res 47:5691–5698, 1987.

    Google Scholar 

  80. Hujanen ES, Terranova VP. Migration of tumor cells to organ-derived chemoattractants. Cancer Res 45:3517–3521, 1985.

    PubMed  CAS  Google Scholar 

  81. Bresalier RS, Hujanen ES, Raper SE, Roll FJ, Itzkowitz SH, Martin GR, Kim YS. An animal model for colon cancer metastasis: Establishment and characterization of murine cell lines with enhanced liver-metastasizing ability. Cancer Res 47:1398–1406, 1987.

    PubMed  CAS  Google Scholar 

  82. Cerra RF, Nathanson SD. Organ-specific chemotactic factors present in lung extracellular matrix. Surg Res 46:422–426, 1989.

    Article  CAS  Google Scholar 

  83. Liotta LA, Mandler R, Murano G, Katz DA, Gordon RK, Chang PK, Schiffman E. Autocrine motility factors. Proc Natl Acad Sci USA 83:3302–3306, 1986.

    Article  PubMed  CAS  Google Scholar 

  84. Atnip KD, Carter LM, Nicolson GL, Dabbous MK. Chemotactic response of rat mammary adenocarcinoma cell clones to tumor-derived cytokines. Biochem Biophys Res Commun 146:996–1002, 1987.

    Article  PubMed  CAS  Google Scholar 

  85. Nabi IR, Watanabi H, Raz A. Identification of B16-F1 melanoma autocrine motility-like factor receptor. Cancer Res 50:409–414, 1990.

    PubMed  CAS  Google Scholar 

  86. Erdel M, Spiess E, Trefz G, Boxberger HJ, Ebert W. Cell interactions and motility in human lung tumor cell lines HS-24 and SB-3 under the influence of extracellular matrix components and proteinase inhibitors. Anticancer Res 12:349–359, 1992.

    PubMed  CAS  Google Scholar 

  87. Salge U, Kilian P, Newmann K, Elsasser HP, Havemann K, Heidtmann HH. Differentiation capacity of human non-small cell lung cancer cell lines after exposure to phorbol ester. Int J Cancer 45:1143–1150, 1990.

    Article  PubMed  CAS  Google Scholar 

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Boyd, D.D., Nicolson, G.L. (1995). Mechanisms of invasion by head and neck cancers. In: Hong, W.K., Weber, R.S. (eds) Head and Neck Cancer. Cancer Treatment and Research, vol 74. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-2023-8_6

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