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Malignant transformation alters intracellular trafficking of lysosomal cathepsin D in human breast epithelial cells

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Pathology & Oncology Research

Abstract

Increased expression and alteration of intracellular trafficking of lysosomal cathepsins have been reported in malignant tumors, or in cells transformed by the transfection with the ras oncogene. In the present study, immortal MCF-10A human breast epithelial cells were transformed with the mutated ras oncogene. Both cell lines were investigated for changes in the intracellular localization of lysosomal cathepsin D and lamp-1 (lysosome-associated membrane protein) employing specific antibodies and confocal immunofluorescence microscopy. The results revealed that staining for cathepsin D along with for lamp-1 was mostly localized in the perinuclear region of MCF-10A cells. In contrast, the staining for these proteins was found to be widely distributed throughout the cytoplasm and at the cell periphery in MCF-10AneoT cells. The organization of microtubules, but not actin, appeared to differ between MCF-10A cells and their oncogenic ras transfectants. When the microtubules were depoly-merized by treatment of MCF-10A cells with nocodazole, vesicles containing the lysosomal cathepsin D were dispersed in the cytoplasm and translocation of these vesicles to the cell periphery was observed. The intracellular localization of cathepsin D in the nocodazole-treated MCF-10A cells seemed to be similar to that observed in the oncogenic ras transfectants of these cells. When taxol, which inhibits microtubule depolymerization, was added to the culture medium of neoT cells, a polymerized microtubule network was observed, and the reclustering of cathepsin D and lamp-1 occurred in a unidirectional manner towards the perinuclear region. These findings support a model in which cytoskeletal microtubule organization is closely related to the trafficking of lysosomes/endodomes, and in which oncogenic ras interferes with such organization in human breast epithelial cells.

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References

  1. Albini A, Graf J, Kitten GT, et al: 17-Estradiol regulates and v-Ha-ras transfection constitutively enhances MCF7 breast cancer cell interactions with basement membrane. Proc Natl Acad Sci USA 83:8182–8186, 1986.

    Article  PubMed  CAS  Google Scholar 

  2. Aniento F, Emans N, Griffiths G, Gruenberg, J: Cytoplasmic dynein-dependent vesicular transport from early to late endo-somes. J Cell Biol 123:1373–1387, 1993.

    Article  PubMed  CAS  Google Scholar 

  3. Basolo F, Elliot J, Tait L, et al: Transformation of human breast epithelial cells by c-Ha-ras oncogene. Mol Carcinogen 4:25–35, 1991.

    Article  CAS  Google Scholar 

  4. Brouillet JP, Spyratos F, Hacene K., et al: Immunoradiometric assay of pro-cathepsin D in breast cancer cytosols-relative prognostic value versus total cathepsin D. Eur J Cancer 29A: 1248–1251, 1993.

    Article  PubMed  CAS  Google Scholar 

  5. Campo E, Munoz J, Miquel R., et al: Cathepsin B expression in colorectal carcinomas correlates with tumor progression and shortened patient survival. Am J Pathol 145:301–309, 1994.

    PubMed  CAS  Google Scholar 

  6. De Brabander M, Geuens G, Nuydens R., et al: Taxol induces the assembly of free microtubules in living cells and blocks the organizing capacity of the centrosomes and kinetochores. Proc Natl Acad Sci USA 78:5608–5612, 1981.

    Article  Google Scholar 

  7. Glotzer M, Hyman AA: The importance of being polar. Curr Biol 5:1102–1105, 1995.

    Article  PubMed  CAS  Google Scholar 

  8. Hasson T, Mooseker MS: Molecular motors, membrane movements and physiology: emerging roles for myosins. Curr Opin Cell Biol 7:587–594, 1995.

    Article  PubMed  CAS  Google Scholar 

  9. Herman B, Albertini DF: The intracellular movement of endo-cytic vesicles in cultured ovarian granulosa cells. Cell Motil 2:583–597, 1982.

    Article  PubMed  CAS  Google Scholar 

  10. Hollenbeck PJ, Swanson JA: Radial extension of macrophage tubular lysosomes supported by kinesin. Nature 346:864–866, 1990.

    Article  PubMed  CAS  Google Scholar 

  11. Honn KV, Timar J, Rozhin J, et al: A Lipoxygenase metabolite, 12-(S)-HETE, stimulates protein kinase C-mediated release of cathepsin B from malignant cells. Exp Cell Res 214.120–130, 1994.

    Article  PubMed  CAS  Google Scholar 

  12. Ichikawa T, Kyprianou N, Isaacs JT: Genetic instability and the acquisition of metastatic ability by rat mammary cancer cells following v-H-ras oncogene transfection. Cancer Res 50:6349–6357, 1990.

    PubMed  CAS  Google Scholar 

  13. Johnson MD, Torri JA, Lippman ME, Dickson RB: The role of cathepsin D in the invasiveness of human breast cancer cells. Cancer Res 53.7873–7877, 1993.

    Google Scholar 

  14. Kageshita T, Yoshii A, Kimura T, et al: Biochemical and immu-nohistochemical analysis of cathepsins B, H, L and D in human melanocytic tumors. Arch Dermatol Res 287:266–272, 1995.

    Article  PubMed  CAS  Google Scholar 

  15. Kane SE, Gottesman MM: The role of cathepsin L in malignant transformation. Semin Cancer Biol 1:127–136, 1990.

    PubMed  CAS  Google Scholar 

  16. Keren Z, LeGrue SJ: Identification of cell surface cathepsin B-like activity on murine melanomas and fibrosarcomas: modulation by butanol extraction. Cancer Res 48:1416–1421, 1988.

    PubMed  CAS  Google Scholar 

  17. Langford GM: Actin- and microtubule-dependent organelle motors: interrelationships between the two motility systems. Curr Opin Cell Biol 7:82–88, 1995.

    Article  PubMed  CAS  Google Scholar 

  18. Lin SXH, Collins CA: Immunolocalization of cytoplasmic dyne-in to lysosomes in cultured cells. J Cell Sci 101:125–137, 1992.

    PubMed  CAS  Google Scholar 

  19. Lippincott-Schwartz J, Cole NB, Marotta A, et al: Kinesin is the motor for microtubule-mediated Golgi-to-ER membrane traffic. J Cell Biol 128:293–306, 1995.

    Article  PubMed  CAS  Google Scholar 

  20. Matteoni R, Kreis TE: Translocation and clustering of endo-somes and lysosomes depends on microtubules. J Cell Biol 105, 1253–1265, 1987.

    Article  PubMed  CAS  Google Scholar 

  21. Miller FR,, Soule HD, Tait L, et al: Xenograft model of human proliferative breast disease. J Natl, Cancer Inst, 85, 1725–1732, 1993.

    Article  CAS  Google Scholar 

  22. Moin K, Sameni M, Elliott E, et al: Ras oncogene alters localization of cathepsins. In Proteases Involved in Cancer, (eds. M Suzuki and T Hiwasa), pp. 51–58, Monduzzi Editore, S.p.A., Bologna, 1994.

    Google Scholar 

  23. Mort JS, Recklies AD: Interrelationship of active and latent secreted human cathepsin B precursors. Biochem J 233:57–63, 1986.

    PubMed  CAS  Google Scholar 

  24. Nakata T, Hirokawa N: Point mutation of adenosine triphos-phate-binding motif generated rigor kinesin that selectively blocks anterograde lysosome membrane transport. J Cell Biol 131:1039–1053, 1995.

    Article  PubMed  CAS  Google Scholar 

  25. Nishimura Y Higaki M, Kato K: Identification of a precursor form of cathepsin D in microsomal lumen: characterization of enzymatic activation and proteolytic processing in vitro. Biochem Biophys Res Commun 148:335–343, 1987.

    Article  PubMed  CAS  Google Scholar 

  26. Nishimura Y Kawabata T, Kato K: Identification of latent procathepsins B and L in microsomal lumen: characterization of enzymatic activation and proteolytic processing in vitro. Arch Biochem Biophys 261:64–71, 1988.

    Article  PubMed  CAS  Google Scholar 

  27. Ochieng J, Basolo F, Albini A, et al: Increased invasive, chemotactic and locomotive abilities of c-Ha-ras-transformed human breast epithelial cells. Invasion Metast 11:38–47, 1991.

    CAS  Google Scholar 

  28. Phaire-Washington L, Silverstein SC, Wang E: Phorbol myristate acetate stimulates microtubule and 10-nm filament extention and lysosome redistribution in mouse macrophages. J Cell Biol 86:641–655, 1980.

    Article  PubMed  CAS  Google Scholar 

  29. Poole AR, Tiltman KJ, Recklies AD, Stoker TAM: Differences in the secretion of the proteinase cathepsin B at the edges of human breast carcinomas and fibroadenomas. Nature 273, 545–547, 1980.

    Article  Google Scholar 

  30. Rempel SA, Rosenblum ML, Mikkelsen T, et al: Cathepsin B expression and localization in glioma progression and invasion. Cancer Res 54:6027–6031, 1994.

    PubMed  CAS  Google Scholar 

  31. Rochefort H: Biological and clinical significance of cathepsin D in breast cancer. Semin Cancer Biol 1:153–160, 1990.

    PubMed  CAS  Google Scholar 

  32. Rochefon H, Capony F, Garcia M: Cathepsin D:a protease involved in cancer metastasis. Cancer Metast Rev 9:321–331. 1990.

    Article  Google Scholar 

  33. Rochefort H: Cathepsin D in breast cancer: A tissue marker associated with metastasis. Fur J Cancer 28 A: 1780–1783, 1992.

    Google Scholar 

  34. Roederer M, Bowser R., Murphy RF: Kinetics and temperature dependence of exposure of endocytosed material to proteolytic enzymes and low pH: evidence for a maturation model for the formation of lysosomes. J Cell Physiol 131, 200–209, 1987.

    Article  PubMed  CAS  Google Scholar 

  35. Rowinsky EK, Cazenave LA, Donehower RC: Taxol: A novel investigational antimicrotubule agent. J Natl Cancer Inst 82:1247–1259, 1990.

    Article  PubMed  CAS  Google Scholar 

  36. Rozhin J, Sameni M, Ziegler G, Sloane BF: Pericellular pH affects distribution and secretion of cathepsin B in malignant cells. Cancer Res 54, 6517–6525, 1994.

    PubMed  CAS  Google Scholar 

  37. Sameni M, Elliott E, Ziegler G, et al: Cathepsin B and D are localized at the surface of human breast cancer cells. Pathol Oncol Res 1:43–53, 1995.

    Article  PubMed  CAS  Google Scholar 

  38. Sloane BF, Honn KV: Cysteine proteinases and metastasis. Cancer Metast Rev 3:249–263, 1984.

    Article  CAS  Google Scholar 

  39. Sloane BF, Rozhin J, Johnson K, et al: Cathepsin B:association with plasma membrane in metastatic tumors. Proc Natl Acad Sci USA 83:2483–2487, 1986.

    Article  PubMed  CAS  Google Scholar 

  40. Sloane BF, Rozhin J, Hatfield JS, et al: Plasma membrane-associated cysteine proteinases in human and animal tumors. Exp Cell Biol 55:209–224, 1987.

    PubMed  CAS  Google Scholar 

  41. Sloane BF: Cathepsin B and cystatins: evidence for a role in cancer progression. Semin Cancer Biol 1:137–152, 1990.

    PubMed  CAS  Google Scholar 

  42. Sloane BF, Moin K, Krepela E, Rozhin J: Cathepsin B and its endogenous inhibitors: role in tumor malignancy. Cancer Metast Rev 9:333–352, 1990.

    Article  CAS  Google Scholar 

  43. Sloane BF, Moin K, Lah TT: Regulation of lysosomal endopep-tidases in malignant neoplasia. In Aspects of the Biochemistry and Molecular Biology of Tumors (eds. TG Pretlow and TP Pretlow), pp.411–466. Academic Press, New York, 1994.

    Google Scholar 

  44. Sloane BF, Moin K, Sameni M, et al: Membrane association of cathepsin B can be induced by transfection of human breast epithelial cells with c-Ha-ras oncogene. J Cell Sci 107:373–384, 1994.

    PubMed  CAS  Google Scholar 

  45. Soule H, Maloney TM, Wolman SR. et al: Isolation and characterization of a spontaneously immortalized human breast epithelial cell line MCF-10. Cancer Res 50, 6075–6086, 1990.

    PubMed  CAS  Google Scholar 

  46. Timar. J, Tang D. Bazaz R, et al: PKC mediates 12-(S)-HETE-induced cytoskeletal rearrangement in B16a melanoma cells. Cell Motil Cytoskel 26: 49–65, 1993.

    Article  CAS  Google Scholar 

  47. Timar J, Bazaz R, Kimler V, et al: Immunomorphological characterization and effects of 12-(S)-HETE on a dynamic intracel-lular pool of the α11bβ3-integrin in melanoma cells..J Cell Sci 108:2175–2186. 1995

    PubMed  CAS  Google Scholar 

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Correspondence to Yukio Nishimura.

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Nishimura, Y., Sameni, M. & Sloane, B.F. Malignant transformation alters intracellular trafficking of lysosomal cathepsin D in human breast epithelial cells. Pathol. Oncol. Res. 4, 283–296 (1998). https://doi.org/10.1007/BF02905219

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