Literature DB >> 2908646

Human mammary epithelial cells in culture: differentiation and transformation.

M R Stampfer, J C Bartley.   

Abstract

Large quantities of normal and malignant human mammary epithelial tissues are readily available as surgical discard material. We have developed culture conditions that permit long term, active proliferation of these HMEC in a serum-free medium. Thus, large pools HMEC can be stored frozen for repetition of experiments from the same individual's cell population, and for use of the same cell pool by multiple investigators. Of all the specimens that we have thus far examined, we have observed no instances of spontaneous transformation to immortality, nor any karyotypic abnormalities in the cells derived from reduction mammoplasties. However, exposure of normal HMEC to the chemical carcinogen, benzo(a)pyrene did lead to expression of an extended life in culture, and two instances of transformation to immortality. These two established cell lines contain some chromosomal abnormalities, yet retain a relatively stable karyotype upon continued passage in culture. Transformation to malignancy was achieved by exposing these cell lines to tumor viruses and oncogenes. Both the normal HMEC, and the HMEC transformed in vitro, are now being utilized to understand the factors controlling expression of mammary specific properties, response to and production of various growth factors, and the nature of the progressive events leading to malignancy. The maximal usefulness of this, and other human epithelial cell systems, for elucidating the mechanisms of normal and diseased human cellular physiology will require continued efforts to optimize the culture conditions so that they resemble as closely as possible the processes occurring in humans in vivo.

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Year:  1988        PMID: 2908646     DOI: 10.1007/978-1-4613-1733-3_1

Source DB:  PubMed          Journal:  Cancer Treat Res        ISSN: 0927-3042


  17 in total

1.  Fidelity of the methylation pattern and its variation in the genome.

Authors:  Toshikazu Ushijima; Naoko Watanabe; Eriko Okochi; Atsushi Kaneda; Takashi Sugimura; Kazuaki Miyamoto
Journal:  Genome Res       Date:  2003-05       Impact factor: 9.043

Review 2.  Can ends justify the means?: telomeres and the mechanisms of replicative senescence and immortalization in mammalian cells.

Authors:  J M Sedivy
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-04       Impact factor: 11.205

3.  Exome-wide mutation profile in benzo[a]pyrene-derived post-stasis and immortal human mammary epithelial cells.

Authors:  Paul L Severson; Lukas Vrba; Martha R Stampfer; Bernard W Futscher
Journal:  Mutat Res Genet Toxicol Environ Mutagen       Date:  2014-11-04       Impact factor: 2.873

4.  Molecular distinctions between stasis and telomere attrition senescence barriers shown by long-term culture of normal human mammary epithelial cells.

Authors:  James C Garbe; Sanchita Bhattacharya; Batul Merchant; Ekaterina Bassett; Karen Swisshelm; Heidi S Feiler; Andrew J Wyrobek; Martha R Stampfer
Journal:  Cancer Res       Date:  2009-09-22       Impact factor: 12.701

Review 5.  Culture models of human mammary epithelial cell transformation.

Authors:  M R Stampfer; P Yaswen
Journal:  J Mammary Gland Biol Neoplasia       Date:  2000-10       Impact factor: 2.673

Review 6.  Xenograft models of premalignant breast disease.

Authors:  F R Miller
Journal:  J Mammary Gland Biol Neoplasia       Date:  2000-10       Impact factor: 2.673

7.  Multiple mechanisms are responsible for transactivation of the epidermal growth factor receptor in mammary epithelial cells.

Authors:  Karin D Rodland; Nikki Bollinger; Danielle Ippolito; Lee K Opresko; Robert J Coffey; Richard Zangar; H Steven Wiley
Journal:  J Biol Chem       Date:  2008-09-09       Impact factor: 5.157

8.  Stepwise DNA methylation changes are linked to escape from defined proliferation barriers and mammary epithelial cell immortalization.

Authors:  Petr Novak; Taylor J Jensen; James C Garbe; Martha R Stampfer; Bernard W Futscher
Journal:  Cancer Res       Date:  2009-06-09       Impact factor: 12.701

9.  An imbalance in progenitor cell populations reflects tumour progression in breast cancer primary culture models.

Authors:  Simona Donatello; Lance Hudson; David C Cottell; Alfonso Blanco; Igor Aurrekoetxea; Martin J Shelly; Peter A Dervan; Malcolm R Kell; Maurice Stokes; Arnold D K Hill; Ann M Hopkins
Journal:  J Exp Clin Cancer Res       Date:  2011-04-26

10.  Exogenous expression of beta-catenin regulates contact inhibition, anchorage-independent growth, anoikis, and radiation-induced cell cycle arrest.

Authors:  K Orford; C C Orford; S W Byers
Journal:  J Cell Biol       Date:  1999-08-23       Impact factor: 10.539

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