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Open AccessJournal Article

Role of serum in the prolactin responsiveness of MCF-7 human breast cancer cells in long-term tissue culture.

Ratna Biswas, +1 more
- 01 Jul 1987 - 
- Vol. 47, Iss: 13, pp 3509-3514
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TLDR
The results clearly demonstrate that, under the proper conditions of culture, the human breast cancer cell line MCF-7 is highly responsive to growth stimulation by homologous lactogenic hormones, and affords an excellent model for further studies on the possible role of prolactin in growth and maintenance of human Breast cancer.
Abstract
MCF-7 human breast cancer cells, grown in long-term tissue culture, were found to be highly responsive to prolactin in terms of growth even in the presence of serum. Human prolactin, placental lactogen, and growth hormone (50–250 ng/ml) stimulated MCF-7 cells to grow when added to culture medium of cells in the presence of charcoal-stripped serum. Within 3 days of the hormone addition, a 4.4-fold increase in cell number was achieved with human prolactin at 100 ng/ml in the presence of 10% charcoal-stripped serum. Under these same conditions, estradiol-17β at 10 -8 m achieved only a 2-fold increase. After 6 days of culture, both estradiol-17β and prolactin gave a total 5-fold increase in cell number. No prolactin effect was achieved in the presence of 10% fetal bovine serum. Stripping fetal bovine serum with dextran-coated charcoal removes as much as 85% of the endogenous lactogens. Removal of these hormones is essential for demonstration of subsequent prolactin-induced growth response in MCF-7 cells, since bovine prolactin binds effectively to lactogen receptors on the surface of the cells but does not transmit a growth signal. When added simultaneously with human prolactin, bovine prolactin blocks the growth response to the former hormone. These results clearly demonstrate that, under the proper conditions of culture, the human breast cancer cell line MCF-7 is highly responsive to growth stimulation by homologous lactogenic hormones. This then affords us an excellent model for further studies on the possible role of prolactin in growth and maintenance of human breast cancer.

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Citations
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Journal ArticleDOI

Prolactin (PRL) and Its Receptor: Actions, Signal Transduction Pathways and Phenotypes Observed in PRL Receptor Knockout Mice

TL;DR: It is clear that there are multiple actions associated with PRL, and the technique of gene targeting in mice has been used to develop the first experimental model in which the effect of the complete absence of any lactogen or PRL-mediated effects can be studied.
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Null mutation of the prolactin receptor gene produces multiple reproductive defects in the mouse.

TL;DR: This work establishes the prolactin receptor as a key regulator of mammalian reproduction, and provides the first total ablation model to further study the role of the prolACTin receptor and its ligands.
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Identification of a cDNA Encoding a Long Form of Prolactin Receptor in Human Hepatoma and Breast Cancer Cells

TL;DR: Human PRL receptor cDNA clones from hepatoma and breast cancer libraries were isolated by using a rat PRL receptors cDNA probe to better understand the role of PRL in the development and growth of human breast cancer.
Journal Article

Expression of prolactin and prolactin receptor in human breast carcinoma. Evidence for an autocrine/paracrine loop.

TL;DR: Analysis of data indicates that prolactin may participate in an autocrine/paracrine stimulatory loop within breast tissues and suggest a role for this growth factor in the pathogenesis of breast cancer.
Journal Article

Prolactin Synthesis and Secretion by Human Breast Cancer Cells

TL;DR: The addition of a panel of anti-human Prl mAbs to T47Dco and MCF7 human breast adenocarcinoma cells suggests that human breast cancer cells synthesize and secrete biologically active Prl.
References
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Journal Article

The effects of androgens and antiandrogens on hormone-responsive human breast cancer in long-term tissue culture.

TL;DR: One of six lines of human breast cancer maintained in long-term tissue culture for at least 1 year and examined for estrogen responsiveness, MCF-7, shows marked stimulation of macromolecular synthesis and cell division with physiological concentrations of estradiol.
Book ChapterDOI

Measurement of growth and viability of cells in culture.

TL;DR: This chapter focuses on cell culture measurements that can be divided into four major categories: visual methods, which employ the use of light microscopy and devices commonly used in hematology; chemical methods,which employ commonly used analytical biochemical procedures adapted to tissue culture; electronic systems using flow-through cells or apertures for measurement of incorporated dyes or cell numbers; and an array of miscellaneous procedures.
Journal Article

Prolactin and Murine Mammary Tumorigenesis: A Review

TL;DR: If prolactin can be shown to influence human breast epithelium in a manner similar to its effect on rodent mammary tissue, then prophylactic and/of chemotherapeutic control of human breast tumorigenesis may be feasible by appropriate drug-mediated Prolactin suppression.
Journal ArticleDOI

Serum-free growth of human mammary epithelial cells: rapid clonal growth in defined medium and extended serial passage with pituitary extract.

TL;DR: A serum-free medium with bovine pituitary extract as the only undefined supplement has been developed for long-term culture of human mammary epithelial cells, enabling multiple experiments over a period of time with cells from a single donor.
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