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Stem cells and the development of mammary cancers in experimental rats and in humans

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Abstract

Evidence based on immunocytochemical staining and ultrastructure suggests that morphological gradations between epithelial and myoepithelial cells, and possibly between epithelial cells and alveolar-like cells occur in terminal ductal structures of rat and human mammary glands. The benign carcinogen-induced rat and benign human mammary tumors can contain epithelial, myoepithelial-like and alveolar-like cells, whereas the malignant counterparts mainly contain only epithelial-like cells. Clonal epithelial cell lines from normal rat mammary glands, benign tumors, and SV40-transformed human mammary glands can differentiate to either myoepithelial-like or alveolar-like cells. In those of the rat, the differentiation processes occur in steps: intermediate cells along the myoepithelial-like pathway resemble intermediates in terminal ductal structures in vivo, and can also generate certain well-differentiated mesenchymal elements of the original tumours. Differentiation of the benign rat cells to alveolar-like cells with mammatrophic hormones and retinoids in vitro leads to a reduction in their tumor-forming ability in vivo. Cell lines from malignant rat mammary tumors of increasing metastatic potential and from human ductal carcinomas largely fail to yield myoepithelial-like or alveolar-like cells and are relatively slow-growing. Growth of the rat mammary epithelial cells in culture is stimulated by a pituitary-derived mammatrophic growth factor (PMGF), prostaglandin E2, and α-transforming growth factor; the response of the malignant cell lines to PMGF is reduced. It is suggested that stem cells exist in the rat and human glands that are capable of differentiating to the other major cell types of the mammary parenchyma, and that during the carcinogenic process they generate genetically unstable cells which lose their ability to differentiate and attempt to maximise their intrinsically slow growth rate.

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References

  1. Hollman KH: Cytology and fine structure of the mammary gland. In: Larson BL and Smith VR (ed). Lactation: a comprehensive treatise, Vol. 1, Academic Press, New York, 1974, pp 3–37

    Google Scholar 

  2. Dawson EK: A histological study of the normal mamma in relation to tumour growth. I. Early development to maturity. Edinburgh Med J 41: 653–682, 1934

    Google Scholar 

  3. Cole HA: The mammary gland of the mouse during the oestrus cycle, pregnacy and lactation. Proc Royal Soc London (Biol) 114: 136–161, 1933

    Google Scholar 

  4. Turner CV, Gomez ET: The normal development of the mammary gland of the male and female albino mouse. Mo Agric Station Res Bull 182: 3–20, 1933

    Google Scholar 

  5. Russo IH, Russo J: Developmental stage of the rat mammary gland as determinant of its susceptibility to 7,12 dimethylbenz[a]anthracene. J Natl Cancer Inst 61: 1439–1449, 1978

    Google Scholar 

  6. Russo J, Tay LK, Russo IH: Differentiation of the mammary gland and susceptibility to carcinogenesis. Breast Cancer Res and Treat 2: 5–73, 1982

    Google Scholar 

  7. Dawson EK: A histological study of the normal mamma in relation to tumour growth. II. The mature gland in pregnancy and lactation. Edinburgh Med J 42: 569–598, 1935

    Google Scholar 

  8. Bassler R: The morphology of hormone induced structural changes in female breast. Curr Top Pathol 53: 1–89, 1970

    Google Scholar 

  9. Salazar H, Tobon H: Morphologic changes of the mammary gland during development, pregnancy and lactation. In: Josinovich JB (ed) Lactogenic hormones, fetal nutrition, and lactation. Wiley, New York, 1974, pp 221–277

    Google Scholar 

  10. Russo J, Russo IH: Influence of differentiation and cell kinetics on the susceptibility of the rat mammary gland to carcinogenesis. Cancer Res 40: 2677–2687, 1980

    Google Scholar 

  11. Dulbecco R, Henahan M, Armstrong B: Cell types and morphogenesis in the mammary gland. Proc Natl Acad Sci USA 79: 7346–7350, 1982

    Google Scholar 

  12. Vorherr H: Development of the female breast. In: The breast, morphology, physiology and lactation. Academic Press, New York, 1974, pp 1–18

    Google Scholar 

  13. Ozzello L: Ultrastructure of the human mammary gland. Pathol Ann 6: 1–58, 1971

    Google Scholar 

  14. Radnor CJP: Myoepithelial cell differentiation in rat mammary glands. J Anat 111: 381–398, 1972

    Google Scholar 

  15. Ceriani RL, Peterson JA: Characterisation of differentiation antigens of the mouse mammary epithelial cell (MME antigens) carried on the mouse milk fat globule. Cell Differ 7: 355–366, 1978

    Google Scholar 

  16. Heyderman E, Steele K, Ormerod MG: A new antigen on the epithelial membrane: its immunoperoxidase localisation in normal and neoplastic tissue. J Clin Path 32: 35–39, 1979

    Google Scholar 

  17. Lane EB: Monoclonal antibodies provide specific intramolecular markers for the study of epithelial tonofilament organization. J Cell Biol 92: 665–673, 1982

    Google Scholar 

  18. Rudland PS: Stem cells in mammary development and cancer. In: Medina D, Kidwell W, Heppner G and Anderson E (eds) Cellular and molecular biology of experimental mammary cancer, Organ Systems Coordinating Center Publications, Roswell Park Memorial Institute, 1987, ch 1.

  19. Hughes CM: Lectin staining of the rat mammary gland. M. Phil. Dissertation, University of London, England, 1987

    Google Scholar 

  20. Monaghan P, Warburton MJ, Perusinghe N, Rudland PS: Topographical arrangement of basement membrane proteins in lactating rat mammary gland: comparison of the distribution of type IV collagen, laminin, fibronectin and Thy-1 at the ultrastructural level. Proc Natl Acad Sci, USA 80: 3344–3348, 1983

    Google Scholar 

  21. Dulbecco R: Immunological markers in the study of development and oncogenesis in the rat mammary gland. J Cell Physiol (Suppl 2): 19–22, 1982

  22. Rudland PS, Warburton MJ, Monaghan P, Ritter MA: Thy-1 antigen on normal and neoplastic rat mammary tissue: changes in location and amount of antigen during differentiation of cultured stem cells. J Natl Cancer Inst 68: 799–811, 1982

    Google Scholar 

  23. Warburton MJ, Mitchell D, Ormerod EJ, Rudland PS: Distribution of myoepithelial cells and basement membrane proteins in the resting, pregnant, lactating and involuting rat mammary gland. J Histochem Cytochem 30: 667–676, 1982

    Google Scholar 

  24. Taylor-Papadimitriou J, Lane EB, Chang SE: Cell lineages and interactions in neoplastic expression in the human breast. In: Rich MA, Hager JC, Furmanski P (eds) Understanding breast cancer, clinical and laboratory concepts. Marcel Dekker Inc, New York, 1983, pp 215–246

    Google Scholar 

  25. Jamieson S, Dunnington DJ, Ormerod EJ, Warburton MJ, Rudland PS: Dedifferentiation of rat mammary myoepithelial-like cell lines after passage in vivo or cloning in vitro. J Natl Cancer Inst 76: 247–256, 1986.

    Google Scholar 

  26. Foster CS, Edwards PAW, Dinsdale EA, Neville AM: Monoclonal antibodies to the human mammary gland: I. Distribution of determinants in non-neoplastic mammary and extramammary tissues. Virchows Arch A (Pathol Anat) 394: 279–293, 1982

    Google Scholar 

  27. Ormerod MG, Steele K, Edwards PAW, Taylor-Papadimitriou J: Monoclonal antibodies that react with epithelial membrane antigen. J Exptl Pathol 1: 263–271, 1984

    Google Scholar 

  28. McIlhinney RAJ, Patel S, Gore ME: Monoclonal antibodies recognise epitopes carried on both glycolipids and glycoproteins of the human milk fat globule membrane. Biochem J 227: 155–162, 1985

    Google Scholar 

  29. Gusterson BA, Warburton MJ, Mitchell D, Ellison M, Neville AM, Rudland PS: Distribution of myoepithelial cells and basment membrane proteins in the normal breast and in benign and malignant breast diseases. Cancer Res 42: 4763–4770, 1982

    Google Scholar 

  30. Gusterson BA; McIlhinney RAJ, Patel S, Knight J, Monaghan P, Ormerod MG: The biochemical and immunocytochemical characterisation of an antigen on the membrane of basal cells of the epidermis. Differentiation 30: 102–110, 1985

    Google Scholar 

  31. Gusterson BA, Monaghan P, Mahendran R, Ellis J, O'Hare MJ: Identification of myoepithelial cells in human and rat breasts by anti-common acute lymphoblastic leukemia antigen antibody A12. J Natl Cancer Inst 77: 343–349, 1986

    Google Scholar 

  32. Radnor CJP: Myoepithelium in the prelactating and lactating mammary glands of the rat. J Anat 112: 337–353, 1972

    Google Scholar 

  33. Newman RA, Klein PJ, Rudland PS: Binding of peanut lectin to breast epithelium, human carcinomas and a cultured rat mammary stem cell and its use as a marker of mammary differentiation. J Natl Cancer Inst 63: 1339–1346, 1979

    Google Scholar 

  34. Herbert DC, Burke RE, McGuire WL: Casein and α-lactalbumin detection in breast cancer cells by immunocytochemistry. Cancer Res 38: 2221–2223, 1978

    Google Scholar 

  35. Earl HM, McIlhinney RAJ: Monoclonal antibodies to human casein. Molecul Immunol 22: 981–991, 1985

    Google Scholar 

  36. Williams JM, Daniel CW: Mammary ductal elongation: differentiation of myoepithelium and basal lamina during branching morphogenesis. Devel Biol 97: 274–290, 1983

    Google Scholar 

  37. Ormerod EJ, Rudland PS: Cellular composition and organisation of ductal buds in developing rat mammary glands: evidence for morphological intermediates between epithelial and myoepithelial cells. Am J Anat 170: 631–652, 1984

    Google Scholar 

  38. Dulbecco R, Unger M, Armstrong B, Bowman M, Syka P: Epithelial cell types and their evolution in the rat mammary gland determined by immunological markers. Proc Natl Acad Sci USA 80: 1033–1037, 1983

    Google Scholar 

  39. Allen R, Dulbecco R, Syka P, Bowman M, Armstrong B: Developmental regulation of cytokeratins in cells of the rat mammary gland studied with monoclonal antibodies. Proc Natl Acad Sci USA 81: 1203–1207, 1984

    Google Scholar 

  40. Stirling JW, Chandler JA: The fine structure of the normal, resting terminal ductal-lobular unit of the female breast. Virchows Arch A (Pathol Anat) 372: 205–226, 1976

    Google Scholar 

  41. Smith CA, Monaghan P, Neville AM: Basal clear cells of the normal human breast. Virchows Arch A (Pathol Anat) 402: 319–329, 1984

    Google Scholar 

  42. Ferguson DJP: Ultrastructural characterisation of the proliferative (stem?) cells within the parenchyma of the normal ‘resting’ breast. Virchows Arch A (Pathol Anat) 407: 379–385, 1985

    Google Scholar 

  43. Hoshino K: Morphogenesis and growth potentiality of mammary glands in mice. II. Quantitative transplantation of mammary glands of normal male mice. J Natl Cancer Inst 30: 585–591, 1963

    Google Scholar 

  44. Hoshino K: Regeneration and growth of quantitatively transplanted mammary glands of normal female mice. Anat Record 150: 221–236, 1964

    Google Scholar 

  45. Ormerod EJ, Rudland PS: Regeneration of mammary glands in vivo from isolated mammary ducts. J Embryol Exptl Morphol 96: 229–243, 1986

    Google Scholar 

  46. Huggins C, Grand LC, Brillantes FP: Mammary cancer induced by a single feeding of polynuclear hydrocarbons and its suppression. Nature 189: 204–207, 1961

    Google Scholar 

  47. Dao TL: Mammary cancer induction by 7,12-dimethyl-benz[a]anthracene: relation to age. Science 165: 810–811, 1969

    Google Scholar 

  48. Russo J, Saby J, Isenburg WM, Russo IH: Pathogenesis of mammary carcinomas induced in rats by 7,12-dimethylbenz[a]anthracene. J Natl Cancer Inst 59: 435–455, 1977

    Google Scholar 

  49. Gullino PM, Pettigrew HM, Grantham FH: N-nitrosomethylurea as mammary gland carcinogen in rats. J Natl Cancer Inst 54: 401–414, 1975

    Google Scholar 

  50. Williams JC, Gusterson BA, Humphreys J, Monaghan P, Coombes RC, Rudland P, Neville AM: N-methyl-N-nitrosourea-induced rat mammary tumors: hormone responsiveness but lack of spontaneous metastasis. J Natl Cancer Inst 66: 147–155, 1981

    Google Scholar 

  51. Kim U: On the immunogenicity of tumor cells and the pattern of metastasis. In: Nicolson GL and Milas L (eds) Cancer invasion and metastasis, biologic and therapeutic aspects. Raven Press, New York, 1984, pp 337–351

    Google Scholar 

  52. Williams JC, Gusterson BA, Coombes RC: Spontaneous metastasising variants derived from MNU-induced rat mammary tumor. Brit J Cancer 45: 588–597, 1982

    Google Scholar 

  53. Kim U: Factors influencing metastasis of breast cancer. In: McGuire WL (ed) Breast cancer, vol 3, Plenum Publishing Corp, New York, 1979, pp 1–49

    Google Scholar 

  54. Williams JC, Gusterson BA, Monaghan P, Coombes RC, Rudland PS: Isolation and characterization of clonal cell lines from a transplantable metastasizing rat mammary tumor, TR2CL. J Natl Cancer Inst 74: 415–428, 1985

    Google Scholar 

  55. Archer FL: Fine structure of spontaneous and estrogeninduced secretion in breast tumors in the rat induced by 7,12 dimethylbenz[a]anthacene. J Natl Cancer Inst 42: 347–362, 1969

    Google Scholar 

  56. Murad TM, von Haam E: The ultrastructure of DMBA-induced breast tumors in Sprague Dawley rats. Acta Cytol 16: 447–453, 1972

    Google Scholar 

  57. Dunnington DJ, Kim U, Hughes CM, Monaghan P, Ormerod EJ, Rudland PS: Loss of myoepithelial cell characteristics in metastasizing rat mammary tumors relative to their nonmetastasizing counterparts. J Natl Cancer Inst 72: 455–466, 1984

    Google Scholar 

  58. Ormerod EJ, Warburton MJ, Gusterson B, Hughes CM, Rudland PS: Abnormal deposition of basement membrane and connective tissue components in dimethylbenzanthracene-induced rat mammary tumours: an immunocytochemical and ultrastructural study. Histochem J 17: 1155–1166, 1985

    Google Scholar 

  59. Supowit SC, Rosen JM: Hormonal induction of casein gene expression is limited to a small subpopulation of 7,12-dimethylbenz[a]anthracene induced mammary cells. Cancer Res 42: 1355–1360, 1982

    Google Scholar 

  60. Rudland PS, Hughes CM, Davies AC, Warburton MJ: Immunocytochemical demonstration of hormonally regulable casein in tumors produced by a rat mammary stem cell line. Cancer Res 43: 3305–3309, 1983

    Google Scholar 

  61. Pitelka DR, Hamamoto ST, Taggart BN: Basal lamina and tissue recognition in malignant mammary tumors. Cancer Res 40: 1600–1611, 1980

    Google Scholar 

  62. Unenormi EN, Ways N, Pitelka DR: Metastasis of murine mammary tumor lines from the mammary gland and ectopic sites. Brit J Cancer 49: 603–614, 1984

    Google Scholar 

  63. McGregor DH, Land CE, Choi K, Tokuoka S, Liv PI: Breast cancer incidence among atomic bomb survivors, Hiroshima and Nagasaki 1950–1969. J Natl Cancer Inst 59: 799–811, 1977

    Google Scholar 

  64. Rudland PS: Animal viruses and cancer: changes in gene organisation in human cancers. In: Davies AJS and Rudland PS (eds) Medical perspectives in cancer research, Ellis Horwood Ltd, Chichester UK, 1985, pp 91–137.

    Google Scholar 

  65. Wellings SR, Jensen HM, Marcum RG: An atlas of subgross pathology of the human breast with special reference to possible precancerous lesions. J Natl Cancer Inst 55: 231–275, 1975

    Google Scholar 

  66. Wellings SR, Yang J: Human mammary pathology: a guide to breast cancer biology. In: Rich MA, Hager JC and Furmanski P (eds) Understanding breast cancer, clinical and laboratory concepts, Marcel Dekker Inc, New York, 1983, pp 27–41

    Google Scholar 

  67. Azzopardi JG: Problems in breast pathology, WB Saunders and Co. Philadelphia, 1979

    Google Scholar 

  68. DeOme KB, Faulkin LJ, Bern HA, Blair PB: Development of mammary tumors from hyperplastic alveolar nodules transplanted into gland-free mammary fat pads of C3H mice. Cancer Res 19: 515–520, 1959

    Google Scholar 

  69. Lee YT: Patterns of metastasis and natural courses of breast carcinoma. Cancer Metastasis Rev 4: 153–172, 1985

    Google Scholar 

  70. Ahmed A: Atlas of the ultrastructure of human breast diseases, Churchill Livingstone, Edinburgh, 1978

    Google Scholar 

  71. Gould VE, Jao W, Battifora H: Ultrastructural analysis in the differential diagnosis of breast tumours. Pathol Res Pract 167: 45–70, 1980

    Google Scholar 

  72. Macartney JC; Roxburgh J, Curran RC: Intracellular filaments in human cancer cells: a histological study. J Pathol 129: 13–20, 1979

    Google Scholar 

  73. Albrechstein R, Nielson M, Wewer U, Engvall E, Ruoslahti E: Basement membrane changes in breast cancer detected by immunohistochemical staining for laminin. Cancer Res 41: 5076–5081, 1981

    Google Scholar 

  74. Barsky SH. Siegal GP, Janotta F, Liotta LA: Loss of basement membrane components by invasive tumors but not by their benign counterparts. Lab Invest 46: Abstract p7A, 1982

  75. Bussolati G, Alfani V, Weber K, Osborn M: Immunocytochemical detection of actin on fixed and embedded tissues: its potential use in routine pathology. J Histochem Cytochem 28: 169–173, 1980

    Google Scholar 

  76. Macartney JC, Trevithick MA; Kricka L, Curran RC: Identification of myosin in human epithelial cancers with immunofluorescence. Lab Invest 41: 437–445, 1979

    Google Scholar 

  77. Hamperl H: The myothelia (myoepithelial cells). Curr Top Pathol 53: 161–210, 1970

    Google Scholar 

  78. Bailey AJ, Sloane JP, Trickey BS, Ormerod MG: An immunocytochemical study of α-lactalbumin in human breast tissue. J Pathol 137: 13–23, 1982

    Google Scholar 

  79. Stevens U, Laurence DJR, Ormerod MG: Antibodies to lactalbumin interfere with its radioimmunoassay in human plasma. Clinical Chim Acta 87: 149–157, 1978

    Google Scholar 

  80. Hallowes RC, Rudland PS, Hawkins RA, Lewis DJ, Bennett DC, Durbin H: Comparison of the effects of hormones on DNA synthesis in cell cultures of non-neoplastic and neoplastic mammary epithelium from rats. Cancer Res 37: 2492–2504, 1977

    Google Scholar 

  81. Rudland PS, Hallowes RC, Durbin H, Lewis D: Mitogenic activity of pituitary hormones on cell cultures of normal and carcinogen-induced tumor epithelium from rat mammary glands. J Cell Biol 73: 561–577, 1977

    Google Scholar 

  82. Rudland PS, Bennett DC, Warburton MJ: Growth and Differentiation of cultured rat mammary epithelial cells. In: Iacobelli S (ed) Hormones and cancer, Raven Press, New York, 1980, pp 255–269

    Google Scholar 

  83. McGrath CM: Cell organization and responsiveness to hormones in vitro: genesis of domes on mammary cultures. Amer J Zool 15: 231–236, 1975

    Google Scholar 

  84. Warburton MJ, Ferns SA, Hughes CM, Rudland PS: Characterisation of rat mammary cell types in primary culture: lectin and antisera to basement membrane and intermediate filament proteins as indicators of cellular heterogeneity. J Cell Sci 79: 287–304, 1985

    Google Scholar 

  85. Kidwell WR, Wicha MS, Salmon D, Liotta LA: Hormonal controls of collagen substratum formation by cultured mammary cells: implications for growth and differentiation. In: Jimenez de Asua L (ed) Control mechanisms in animal cells, Raven Press, New York, 1980, pp 333–340

    Google Scholar 

  86. Wicha MS, Lowrie G, Kohn E, Bagavandoss P, Mahn T: Extracellular matrix promotes mammary epithelial growth and differentiation in vitro. Proc Natl Acad Sci USA 79: 3213–3217, 1982

    Google Scholar 

  87. Richards J, Hamamoto S, Smith S, Pasco D, Guzman R, Nandi S: Response of end bud cells from immature rat mammary gland to hormones when cultured in collagen gel. Exptl Cell Res 147: 95–109, 1983

    Google Scholar 

  88. Ormerod EJ, Rudland PS: Isolation and characterisation of cloned epithelial cell lines from normal rat mammary glands. In Vitro 21: 143–153, 1985

    Google Scholar 

  89. Bennett DC, Peachey LA, Durbin H, Rudland PS: A possible mammary stem cell line. Cell 15: 296–308, 1978

    Google Scholar 

  90. Dunnington DJ, Monaghan P, Hughes CM, Rudland PS: Phenotypic instability of rat mammary tumor epithelial cells. J Natl Cancer Inst 71: 1227–1240, 1983

    Google Scholar 

  91. Dulbecco R, Henahan M, Bowman M, Okada S, Battifora H, Unger M: Generation of fibroblast-like cells from cloned epithelial mammary cells in vitro: a possible new cell type. Proc Natl Acad Sci USA 78: 2345–2349, 1981

    Google Scholar 

  92. Rudland PS, Bennett DC, Warburton MJ: Hormonal control of growth and differentiation of cultured rat mammary gland epithelial cells. Cold Spr Hb Symp Cell Proliferation 6: 677–699, 1979

    Google Scholar 

  93. Dexter DL, Kowalski HM, Blazar BA, Fligiel S, Vogel R, Heppner GH: Heterogeneity of tumor cells from a single mouse mammary tumor. Cancer Res 38: 3174–3181, 1978

    Google Scholar 

  94. Hager JC, Fligiel S, Stanley W, Richardson AM, Heppner GH: Characterization of a variant producing tumor cell line from a heterogeneous strain Balb/cfC3H mouse mammary tumor. Cancer Res 41: 1293–1300, 1981

    Google Scholar 

  95. Ormerod EJ, Rudland PS: Mammary gland morphogenesis in vitro: formation of branched tubules in collagen gels by a cloned rat mammary cell line. Devel Biol 91: 360–375, 1982

    Google Scholar 

  96. Warburton MJ, Ferns SA, Rudland PS: Enhanced synthesis of basement membrane proteins during the differentiation of rat mammary tumour epithelial cells into myoepithelial-like cells in vitro. Exptl Cell Res 137: 373–380, 1982

    Google Scholar 

  97. Warburton MJ, Head LP, Rudland PS: Redistribution of fibronectin and cytoskeletal proteins during the differentiation of rat mammary tumour cells. Exptl Cell Res 132: 57–66, 1981

    Google Scholar 

  98. Warburton MJ, Ormerod EJ, Monaghan P, Ferns S, Rudland PS: Characterisation of a myoepithelial cell line derived from a neonatal rat mammary gland. J Cell Biol 91: 827–836, 1981

    Google Scholar 

  99. Rudland PS, Paterson FC, Monaghan P, Davies AC, Warburton MJ: Isolation and properties of rat cell lines morphologically intermediate between cultured mammary epithelial and myoepithelial cells. Devel Biol 113: 388–405, 1986

    Google Scholar 

  100. Rudland PS, Bennett DC, Ritter MA, Newman RA, Warburton MJ: Differentiation of a rat mammary stem cell line in culture. In: Jimenez de Asua L (ed) Control mechanisms in animal cells, Raven Press, New York, 1980, pp 341–365

    Google Scholar 

  101. Friend C, Scher W, Holland JG, Sato T: Hemoglobin synthesis in murine virus-induced leukemic cells in vitro: stimulation of erythroid differentiation by dimethyl sulfoxide. Proc Natl Acad Sci USA 68: 378–382, 1971

    Google Scholar 

  102. Rudland PS, Davies AT, Warburton MJ: Prostaglandin induced differentiation or dimethyl sulfoxide-induced differentiation: reduction of the neoplastic potential of a rat mammary tumor stem cell line. J Natl Cancer Inst 69: 1083–1093, 1982

    Google Scholar 

  103. Rudland PS, Paterson FC, Davies AT, Warburton MJ: Retinoid-specific induction of differentiation and reduction of the DNA synthesis rate and tumor-forming ability of a stem cell line from a rat mammary tumor. J Natl Cancer Inst 70: 949–958, 1983

    Google Scholar 

  104. Warburton MJ, Head LP, Ferns SA, Rudland PS: Induction of differentiation in a rat mammary epithelial stem cell line by dimethyl sulphoxide and mammatrophic hormones. Europ J Biochem 133: 707–715, 1983

    Google Scholar 

  105. Bennett DC: Morphogenesis of branching tubules in cultures of cloned mammary epithelial cells. Nature 285: 657–659, 1980

    Google Scholar 

  106. Ormerod EJ, Warburton MJ, Hughes CM, Rudland PS: Synthesis of basement membrane proteins by rat mammary epithelial cells. Devel Biol 96: 269–275, 1983

    Google Scholar 

  107. Ormerod EJ, Rudland PS: Mammary gland morphogenesis in vitro: extracellular requirements for the formation of tubules in collagen gels by a cloned rat mammary cell line. In Vitro: In press

  108. Hallowes RC, Millis R, Pigott D, Shearer M, Stoker MGP, Taylor-Papadimitriou J: Results on a pilot study of cultures of human lacteal secretions and benign and malignant breast tumors. J Clin Oncol 3: 81–90, 1977

    Google Scholar 

  109. Stampfer M, Hallowes RC, Hackett AJ: Growth of normal human mammary cells in culture. In Vitro 16: 414–425, 1980

    Google Scholar 

  110. Kirkland WL, Yang N-S, Jorgensen T, Longley C, Furmanski P: Growth of normal and malignant human mammary epithelial cells in culture. J Natl Cancer Inst 63: 29–41, 1979

    Google Scholar 

  111. Easty GC, Easty DM, Monaghan P, Ormerod MG, Neville AM: Preparation and identification of human breast epithelial cells in culture. Int J Cancer 26: 577–584, 1980

    Google Scholar 

  112. Gusterson BA, Williams J, Bunnage H, O'Hare MJ, Dubois JD: Human breast epithelium transplated into nude mice. Virchows Arch A (Pathol Anat) 404: 325–333, 1984

    Google Scholar 

  113. Yang N-S, Kube D, Park C, Furmanski P: Growth of human mammary epithelial cells on collagen gel surfaces. Cancer Res 41: 4093–4100, 1981

    Google Scholar 

  114. Foster CS, Smith CA, Dinsdale EA, Monaghan P, Neville AM: Human mammary gland morphogenesis in vitro: the growth and differentiation of normal breast epithelium in collagen gel cultures defined by electron microscopy, monoclonal antibodies and autoradiography. Devel Biol 96: 197–216, 1983

    Google Scholar 

  115. Smith CA, Bunnage H, Monaghan P, Neville AM: Human breast epithelium in vitro: the re-expression of structural and functional cellular differentiation in longterm culture. Cell Tissue Res 247: 433–440, 1987

    Google Scholar 

  116. Edwards PAW, Brooks IM, Monaghan P: Antigenic subsets of human breast epithelial cells distinguished by monoclonal antibodies. Differentiation 25: 247–258, 1984

    Google Scholar 

  117. Sloane JP, Ormerod MG: Distribution of epithelial membrane antigen in normal and neoplastic tissues and its value in diagnostic tumor pathology. Cancer 47: 1786–1795, 1981

    Google Scholar 

  118. Stoker MGP, Perryman M, Eeles R: Clonal analysis of morphological phenotype in cultured mammary epithelial cells from human milk. Proc Royal Soc London Series B 215: 231–240, 1982

    Google Scholar 

  119. Edwards PAW, Brooks IM, Bunnage HJ, Foster AV, Ellison ML, O'Hare MJ: Clonal analysis of expression of epithelial antigens in cultures of normal human breast. J Cell Sci 80: 91–101, 1986

    Google Scholar 

  120. Joshi K, Smith JA, Perusinghe N, Monaghan P: Cell proliferation in the human mammary epithelium: differential contribution by epithelial and myoepithelial cells. Am J Pathol 124: 199–206, 1986

    Google Scholar 

  121. Chang SE, Keen J, Lane EB, Taylor-Papadimitriou J: Establishment and characterization of SV40-transformed human breast epithelial cell lines. Cancer Res 42: 2040–2053, 1983

    Google Scholar 

  122. Rudland PS, Ferns SA, Monaghan P, Hughes CM, Barraclough R: Isolation of simian virus 40 transformed human mammary epithelial stem cell lines: differentiation to myoepithelial-like cells is associated with increased expression of large T antigen: In preparation

  123. Taylor-Papadimitriou J, Shearer M, Tilly R: Some properties of cells cultured from early lactation milk. J Natl Cancer Inst 58: 1563–1571, 1977

    Google Scholar 

  124. Rogers CS, Hill SM, Hulten MA, Chang SE, Keen J, Taylor-Papadimitriou J: Cytogenetic analysis of SV40-transformed human breast epithelial cells. Cancer Gen Cytogen 8: 213–221, 1983

    Google Scholar 

  125. Paterson FC, Graham JM, Rudland PS: The effect of ionophores and related agents on the induction of doming in a rat mammary epithelial cell line. J Cell Physiol 123: 89–100, 1985

    Google Scholar 

  126. Paterson FC, Warburton MJ, Rudland PS: Differentiation of mammary epithelial stem cells to alveolar-like cells in culture: cellular pathways and kinetics of the conversion process. Devel Biol 107: 301–313, 1985

    Google Scholar 

  127. Paterson FC, Rudland PS: Identification of novel, stage-specific polypeptides associated with the differentiation of mammary epithelial stem cells to alveolar-like cells in culture. J Cell Physiol 124: 525–538, 1985

    Google Scholar 

  128. Barraclough R, Dawson KJ, Rudland PS: Control of protein synthesis in cuboidal rat mammary epithelial cells in culture: changes in gene expression accompany the formation of elongated cells. Europ J Biochem 129: 336–341, 1982

    Google Scholar 

  129. Paterson FC, Rudland PS: Microtubule-disrupting drugs increase the frequency of conversion of a rat mammary epithelial stem cell line to elongated, myoepithelial-like cells in culture. J Cell Physiol 125: 135–150, 1985

    Google Scholar 

  130. Barraclough R, Kimbell R, Rudland PS: Enhanced expression of a normal cell mRNA sequence accompanies the conversion of rat mammary cuboidal epithelial cells to an elongated morphology in culture. Nucleic Acid Res 21: 8097–8114, 1984

    Google Scholar 

  131. Differential control of mRNA levels for Thy-1 antigen and laminin in rat mammary epithelial and myoepithelial-like cells. J Cell Physiol in press

  132. Warburton MJ, Kimbell R, Rudland PS, Ferns SA, Barraclough R: Control of type IV collagen production in rat mammary epithelial and myoepithelial-like cells. J Cell Physiol 128: 76–84, 1986

    Google Scholar 

  133. Barraclough R, Dawson KJ, Rudland PS: Elongated cells derived from rat mammary cuboidal epithelial cell lines resemble cultured mesenchymal cells in their pattern of protein synthesis. Biochem Biophys Res Comm 120: 351–358, 1984

    Google Scholar 

  134. Rudland PS, Dunnington DJ, Gusterson B, Monaghan P, Hughes CM: Production of skeletal muscle elements by cell lines derived from neoplastic rat mammary epithelial stem cells. Cancer Res 44: 2089–2102, 1984

    Google Scholar 

  135. Rudland PS, Gusterson BA, Hughes CM, Ormerod EJ, Warburton MJ: A neoplastic rat mammary stem cell line generates two forms of tumours in nude mice. Cancer Res 42: 5196–5208, 1982

    Google Scholar 

  136. Dao TL, Bock FG, Greiner MJ: Mammary carcinogenesis by 3-methylcholanthrene. II. Inhibitory effect of pregnancy and lactation on tumor induction. J Natl Cancer Inst 25: 991–1003, 1960

    Google Scholar 

  137. Moon RC: Relationship between previous reproductive history and chemical induced mammary cancer in rats. Int J Cancer 4: 312–317, 1969

    Google Scholar 

  138. Sporn MB, Newton DL: Chemoprevention of cancer with retinoids. Fed Proc 38: 2528–2534, 1979

    Google Scholar 

  139. McCormick DL, Burns FJ, Albert RE: Inhibition of rat mammary carcinogenesis by short dietary exposure to retinyl acetate. Cancer Res 40: 1140–1143, 1980

    Google Scholar 

  140. Thompson HJ, Becci PJ, Brown CC, Moon RC: Effect of the duration of retinyl acetate feeding on inhibition of 1-methyl-1-nitrosourea-induced mammary carcinogenesis in the rat. Cancer Res 39: 3977–3980, 1979

    Google Scholar 

  141. MacMahon B, Cole P, Brown J: Etiology of human breast cancer: a review. J Natl Cancer Inst 50: 21–42, 1973

    Google Scholar 

  142. Peto R, Doll R, Buckley JD, Sporn MB: Can dietary betacarotene materially reduce human cancer rates. Nature 290: 201–208, 1981

    Google Scholar 

  143. Ghosh S, Roholt OA, Kim U: Establishment of two non-metastasizing and one metastasizing rat mammary carcinoma cell lines. In Vitro 19: 919–928, 1983

    Google Scholar 

  144. Rudland PS, Dunnington DJ, Kim U, Gusterson BA, O'Hare MJ, Monaghan P: Alterations in the tumorigenic and metastatic properties of cultured SMT-2A rat mammary tumor cells following transplantation in athymic mice. Submitted

  145. Neri A, Welch D, Kawaguchi T, Nicolson GL: Development and biological properties of malignant cell sublines and clones of spontaneously metastasizing rat mammary adenocarcinoma. J Natl Cancer Inst 68: 507–517, 1982

    Google Scholar 

  146. Dunnington DJ, Kim U, Hughes CM, Monaghan P, Rudland PS: Lack of production of myoepithelial variants by cloned epithelial cell lines derived from the TMT-081 metastasizing rat mammary tumor. Cancer Res 44: 5338–5346, 1984

    Google Scholar 

  147. Rudland PS, Jimenez de Asua L: The action of growth factors in the cell cycle. Biochim Biophys Acta 560: 91–133, 1979

    Google Scholar 

  148. Rudland PS, Jimenez de Asua L: The action of growth factors in normal and transformed cells. Brit J Cancer 39: 464–465, 1979

    Google Scholar 

  149. North SM, Nicolson GL: Effect of host immune status on the spontaneous metastasis of clonal cell lines of the 13762NF rat mammary adenocarcinoma. Brit J Cancer 52: 747–755, 1985

    Google Scholar 

  150. Dunnington DJ: The development and study of single cell-cloned metastasizing mammary tumour cell systems in the rat. Ph D Dissertation, University of London, England, 1984

    Google Scholar 

  151. Nowell PC: The clonal evolution of tumor cell populations. Science 194: 23–28, 1976

    Google Scholar 

  152. Nicolson GL, Steck PA, Welch DR, Lembo TM: Heterogeneity and instability of phenotypic and metastatic properties of local tumor- and metastasis-derived clones of a mammary adenocarcinoma. In: Rich MA, Hager JC, Furmanski P (eds) Understanding breast cancer, clinical and laboratory concepts, Marcel Dekker Inc, New York, 1983, pp 145–166

    Google Scholar 

  153. Poste G: Tumor cell biology and the metastatic process. In: Rich MA, Hager JC, Furmanski P (eds) Understanding breast cancer, clinical and laboratory concepts, Marcel Dekker Inc, New York, 1983, pp 119–144

    Google Scholar 

  154. Welch DR, Nicolson GL: Phenotypic drift and heterogeneity in response to metastatic mammary adenocarcinoma cell clones to adriamycin, 5-fluoro-2-deoxyuridine and methotrexate treatment in vitro. Clin Exptl Metastasis 1: 317–325, 1983

    Google Scholar 

  155. Tomasovic SP, Thames HD, Nicolson GL: Heterogeneity in hyperthermic sensitivities of rat 13762NF mammary adenocarcinoma cell clones of differing metastatic potentials. Radiat Res 91: 555–563, 1982

    Google Scholar 

  156. Welch DR, Milas L, Tomasovic SP, Nicolson GL: Heterogeneous response and clonal drift of sensitivities of metastatic 13762NF mammary adenocarcinoma clones to γ-radiation in vitro. Cancer Res 43: 6–10, 1983

    Google Scholar 

  157. Rudland PS: The relationship of the transformed cell in culture to the malignant breast cancer cell. In: Cellular aspects of breast cancer. Ciba Gergy, Media Medica Ltd, Liphock Hamps, 1985

    Google Scholar 

  158. Beuhring GC, Williams RR: Growth rates of normal and abnormal mammary epithelia in cell culture. Cancer Res 36: 3742–3746, 1976

    Google Scholar 

  159. Lasfargues EY, Ozzello L: Cultivation of human breast carcinomas. J Natl Cancer Inst 21: 1131–1147, 1958

    Google Scholar 

  160. Nordquist RE; Ishmael DR; Lovig CA: The tissue culture and morphology of human breast tumor cell line BOT-2. Cancer Res 35: 3100–3105, 1975

    Google Scholar 

  161. Hackett AJ, Smith HS; Springer EL; Owens RB, Nelson-Rees WA, Riggs JL, Gardner MB: Two syngeneic cell lines from human breast tissue; the aneuploid mammary epithelial (Hs578T) and the diploid myoepithelial (Hs598Bst) cell lines, J Natl Cancer Inst 58: 1705–1806, 1977

    Google Scholar 

  162. Lasfargues EY, Coutinko WG, Redfield ES: Isolation of two human tumor epithelial cell lines from solid breast carcinomas. J Natl Cancer Inst 61: 967–978, 1978

    Google Scholar 

  163. Hallowes RC, Peachey LA, Cox S: Epithelium from human breast cancers in cultures: is it really cancer. In Vitro 19: 286, 1983

    Google Scholar 

  164. Rudland PS, Hallowes RC, Cox SA, Ormerod EJ, Warburton MJ: Loss of production of myoepithelial cells and basement membrane proteins but retention of response to certain growth factors and hormones by a new malignant human breast cancer cell strain. Cancer Res 45: 3864–3877, 1985

    Google Scholar 

  165. Smith HS, Lan S, Ceriani R, Hackett AJ, Stampfer MR: Clonal proliferation of cultured nonmalignant and malignant human breast epithelia. Cancer Res 41: 4637–4643, 1981

    Google Scholar 

  166. Cailleau RM: Old and new problems in human tumor cell cultivation. In: Fogh J (ed) Human tumor cells in vitro, Plenum Publishing Corp, New York, 1975, pp 79–114

    Google Scholar 

  167. Langlois AJ, Holder WD, Iglehart JD, Nelson-Rees WA, Welds SA, Bolognesi DP: Morphological and biochemical properties of a new human breast cancer cell line. Cancer Res 39: 2604–2613, 1979

    Google Scholar 

  168. Whitehead RH, Bertoncello I, Webber LM, Pedersen JS: A new human breast carcinoma cell line (PMC42) with stem cell characteristics. 1. Morphological characterisation. J Natl Cancer Inst 70: 649–661, 1983

    Google Scholar 

  169. Feller WF, Stewart SE, Kanton J: Primary tissue culture expiants of human breast cancer. J Natl Cancer Inst 48: 1117–1120, 1972

    Google Scholar 

  170. Owens RB, Smith HS, Nelson-Rees WA, Springer EL: Epithelial cell cultures from normal and cancerous human tissues. J Natl Cancer Inst 56: 843–849, 1976

    Google Scholar 

  171. Engel LW, Young NA, Tralka TS, Lippman ME, O'Brien SJ, Joyce MJ: Establishment and characterization of three new continuous cell lines derived from human breast carcinomas. Cancer Res 38: 3352–3364, 1978

    Google Scholar 

  172. Semen G, Hunter SJ, Miller RC, Dmochowski L: Characterisation of an established cell line (SH-3) derived from plural effusion of a patient with breast cancer. Cancer 37: 1814–1824, 1976

    Google Scholar 

  173. McManus MJ, Welsch CW: DNA synthesis of benign human breast tumors in the untreated athymic ‘nude” mouse. Cancer 45: 2160–2165, 1980

    Google Scholar 

  174. Smith HS, Wolman SR, Hackett AJ: The biology of breast cancer at the cellular level. Biochem Biophys Acta 738: 103–123, 1984

    Google Scholar 

  175. Monaghan P, Whitehead RH, Perusinghe N, O'Hare MJ: An immunocytochemical and ultrastructural study of heterogeneity in the human breast carcinoma cell line PMC-42. Cancer Res 45: 5088–5097, 1985

    Google Scholar 

  176. Barsky SH, Togo S, Garbisa S, Liotta LA: Type IV collagenase immunoreactivity in invasive breast carcinoma. Lancet 8319: 296–297, 1983

    Google Scholar 

  177. Lyons RW, Li CH, Johnson RE: The hormonal control of mammary growth and lactation and the growth of tumors, Recent Prog Horm Res 94: 219–254, 1958

    Google Scholar 

  178. Nandi S: Endocrine control of mammary gland development and function in the C3H/HcCrgl mouse. J Natl Cancer Inst 21: 1039–1055, 1958

    Google Scholar 

  179. Smith JA, Winslow DP, Rudland PS: Different growth factors stimulate cell division of rat mammary epithelial, myoepithelial and stromal cell lines in culture. J Cell Physiol 119: 320–326, 1984

    Google Scholar 

  180. Jimenez de Asua L, Richmond V, Otto AM, Kubler AM, O'Farrell MK, Rudland PS: Growth factors and hormones interact in a series of temporal steps to regulate the rate of initiation of DNA synthesis in mouse fibroblasts. Cold Spr Hb Conf Cell Prolif 6: 403–424, 1979

    Google Scholar 

  181. Gospodarowicz D: Localisation of a fibroblast growth factor and its effect alone and with hydrocortisone on 3T3 cell growth. Nature 249: 123–127, 1974

    Google Scholar 

  182. Rudland PS, Seifert WE, Gospodarowicz D: Growth control and mitogenic response in cultured mouse fibroblasts: induction of the pleiotypic and mitogenic responses by a purified growth factor. Proc Natl Acad Sci USA 71: 2600–2604, 1974

    Google Scholar 

  183. Smith JA, Winslow DP, O'Hare MJ, Rudland PS: Brain and pituitary fibroblast growth factor activities behave identically on three independent high performance liquid chromatography systems. Biochem Biophys Res Comm 119: 311–318, 1984

    Google Scholar 

  184. Beuving LJ, Bern HA, DeOme KB: Occurrence and transplantation of carcinogen-induced hyperplastic nodules in Fischer rats. J Natl Cancer Inst 39: 431–447, 1967

    Google Scholar 

  185. Gould MN, Biel WF, Clifton KH: Morphological and quantitative studies of gland formation from inocula of monodispersed rat mammary cells. Exptl Cell Res 107: 405–416, 1977

    Google Scholar 

  186. Kratachowil K: Organ specificity in mesenchymal induction demonstrated in the embryonic development of the mammary gland of the mouse. Devel Biol 20: 46–71, 1969

    Google Scholar 

  187. Sakakura T, Nishizuka T, Dawe C. Mesenchyme dependent morphogenesis and epithelial-specific cytodifferentiation in mouse mammary gland. Science 194: 1439–1441, 1976

    Google Scholar 

  188. Sakakura T, Sakagami Y, Nishizuka Y: Dual origin of mesenchymal tissues participating in mouse mammary gland embryogenesis. Devel Biol 91: 202–207, 1982

    Google Scholar 

  189. Rudland PS, Davies AC, Tsao S-W: Rat mammary preadipocytes in culture produce a trophic agent for mammary epithelia-prostaglandin E2. J Cell Physiol 120: 364–376, 1984

    Google Scholar 

  190. Marquardt H, Hunkapiller MW, Hood LE, Todaro GJ: Rat transforming growth factor Type 1: structure and relation to epidermal growth factor. Science 223: 1079–1082, 1984

    Google Scholar 

  191. Smith JA, Ham J, Winslow DP, O'Hare MJ, Rudland PS: The use of HPLC in the isolation and characterisation of mouse and rat epidermal growth factors and examination of their apparent heterogeneity. J Chromatogr 305: 295–308, 1984

    Google Scholar 

  192. Simpson RJ, Smith JA, Moritz RL, O'Hare MJ, Rudland PS, Morrison JR, Lloyd CJ, Grego B, Burgess AW, Nice EC: Rat epidermal growth factor: complete amino acid sequence. Europ J Biochem 153: 629–637, 1985

    Google Scholar 

  193. Rayter Z: Glycoprotein expression in human squamous and breast careinoma. Ph.D Dissertation, University of London, England, 1987

    Google Scholar 

  194. Azzopardi JG et al: Histological typing of breast tumors (2nd edition). In. International histological classification of tumours, Vol 2, WHO, Geneva, 1981

    Google Scholar 

  195. Sloane JP: Infiltrating carcinoma. In: Biopsy pathology of the breast, Chapman and Hall, London, 1985, pp 147–200

    Google Scholar 

  196. Jamieson S: Induction of metastatic ability in benign rat mammary epithelial cells by DNA transfection experiments. Ph.D Dissertation, University of London, England, 1987

    Google Scholar 

  197. Sukumar S, Notario V, Martin-Zanca D, and Barbacid M: Induction of mammary carcinomas in rats by nitrosomethylurea involves malignant activation of H-ras-1 locus by single point mutations. Nature 306: 658–661, 1983

    Google Scholar 

  198. Mak TW, Tannock I (eds): Cellular and molecular biology of neoplasia, AR Liss Inc. New York, 1984

    Google Scholar 

  199. Dynan WS, Tjian R: Isolation of transcription factors that discriminate between different promoters recognized by RNA polymerase II. Cell 32: 669–680, 1983

    Google Scholar 

  200. Tjian R: T antigen binding and the control of SV40 gene expression. Cell 26: 1–2, 1981

    Google Scholar 

  201. Schiffer LM: The cell kinetics of mammary cancers. In: McGuire WL (ed) Breast cancer advances in research and treatment, Vol 2, Plenum Press, New York, 1978, pp 259–282

    Google Scholar 

  202. Fournier DV, Weber E, Hoeffken W, Bauer M, Kubli E, Barth V: Growth rate of 147 mammary carcinomas. Cancer 45: 2198–2207, 1980

    Google Scholar 

  203. Tubiana M, Pejovic MJ, Renaud A, Contesso G, Chavaudra N, Gioanni J, Malaise LP: Kinetic parameters and the course of the disease in breast cancer. Cancer 47: 937–943, 1981

    Google Scholar 

  204. Vorherr H: Breast cancer, Urban and Schwarzenberg Inc, Baltimore-Munich, 1980

    Google Scholar 

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Rudland, P.S. Stem cells and the development of mammary cancers in experimental rats and in humans. Cancer Metast Rev 6, 55–83 (1987). https://doi.org/10.1007/BF00047609

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