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Two new estrogen-supersensitive variants of the MCF-7 human breast cancer cell line
Authors:Clara Natoli MD  Gigliola Sica MD  Vittoria Natoli ScD  Angelo Serra PhD  Stefano Iacobelli MD
Institution:1. Laboratorio di Endocrinologia Molecolare, Università Cattolica del S. Cuore Largo Gemelli, 8-00168, Roma, Italy
2. Istituto di Istologia ed Embriologia Generale, Università Cattolica del S. Cuore Largo Gemelli, 8-00168, Roma, Italy
3. Istituto di Genetica Umana, Università Cattolica del S. Cuore Largo Gemelli, 8-00168, Roma, Italy
4. Laboratorio di Endocrinologia Molecolare, Università Cattolica del S. Cuore Largo Gemelli, 8-00168, Roma, Italy
Abstract:Two new estrogen-sensitive variants of MCF-7 human breast cancer cells, CG-4 and CG-5, are described in this report. These cells were derived from a casual contamination by MCF-7 cells of primary cultures from a human adenocarcinoma of the breast and a pleural effusion of a patient with advanced breast cancer, respectively. Careful characterization of these variants revealed chromosomal properties highly similar to and alloenzyme phenotypes identical to those of MCF-7 cells which were simultaneously cultured in the laboratory. MCF-7, CG-4 and CG-5 cells were tested for estrogen responsiveness under identical growth conditions, that is in the presence of culture medium supplemented with 5% charcoal-treated serum. While the number of MCF-7 cells increases by about 40% over the controls in the presence of physiological concentrations of estradiol, the number of CG-4 cells doubles and the number of CG-5 cells triples. All these cell lines have approximately the same number of estrogen, androgen, glucocorticoid, and progesterone receptor sites/cell. Since several difficulties arise in demonstrating the estrogen responsive growth stimulation of currently available human breast cancer cells, these two new variants, characterized by a high and reproducible estrogen responsiveness, afford a new model for studying the mechanisms by which estrogen regulates cell proliferation. The problems related to the careful characterization of every established cell line are discussed.
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