Mode of estrogen action on cell proliferative kinetics in CAMA-1 cells. I. Effect of serum and estrogen.

Both serum and estrogen affect cell proliferation in CAMA-1 cells. Their effects on cell cycle kinetics are being investigated with partially synchronized cells following 48 hours of serum deprivation. By comparing the growth kinetics of synchronized (serum-deprived) cells with asynchronized (normal-fed) cells, we observed that there was a delay of cell proliferation for approximately 25 hr for synchronized cells and that estrogen only induced cell proliferation in serum-supplemented culture. A serum protein (RPF), precipitated by ammonium sulfate, dialyzed in 3,500 daltons cut off membrane and reconstituted in culture medium, was shown to stimulate cell proliferation in a dose-related manner. In the absence of RPF, estrogen had no effect on cell growth and S-phase formation in serum-free medium, but significantly induced cell growth in the presence of RPF. Experiments conducted with a synchronized cell population showed that estrogen increased the proportion of G1 phase cells to enter S phase, shortened the G1 phase duration, and ultimately increased the proportion of mitotic cells per cycle. Collectively, these results show that (a) estrogen effects of cell proliferation in vitro requires a serum component, a "G1/S-promoting factor" and (b) estrogen-induced tumor growth is a result of an accelerated rate of G1/S transition and an increased number of dividing cells per cycle. The knowledge of the interaction of estrogen with the G1/S promoting factor on cell growth is of both fundamental and therapeutic importance.

[1]  B. Leung,et al.  Mode of estrogen action on cell proliferation in CAMA‐1 cells: II. Sensitivity of G1 phase population , 1987, Journal of cellular biochemistry.

[2]  M. Dell'aquila,et al.  Response of malignant mammary cell lines to a growth inhibitor partially purified from plasma-derived human serum. , 1984, Journal of the National Cancer Institute.

[3]  P. Darbre,et al.  Effects of estradiol and tamoxifen on human breast cancer cells in serum-free culture. , 1984, Cancer research.

[4]  I. Christensen,et al.  Effects of the antioestrogen tamoxifen on the cell cycle kinetics of the human breast cancer cell line, MCF-7. , 1984, British Journal of Cancer.

[5]  L. Murphy,et al.  Effects of biologically active metabolites of tamoxifen on the proliferation kinetics of MCF-7 human breast cancer cells in vitro. , 1983, Cancer research.

[6]  W. Pledger,et al.  A model of cell cycle control: Sequential events regulated by growth factors , 1983, Molecular and Cellular Endocrinology.

[7]  P. Berlinski,et al.  Steroid stimulation of plasminogen activator production in a human breast cancer cell line (MCF-7). , 1983, Cancer research.

[8]  J. Field,et al.  Serum regulation of the estrogen responsiveness of the human breast cancer cell line MCF-7. , 1983, Cancer research.

[9]  B. Leung,et al.  Response to estrogen by the human mammary carcinoma cell line CAMA-1. , 1982, Cancer research.

[10]  D. Edwards,et al.  Immunohistochemical detection of an estrogen-regulated protein by monoclonal antibodies. , 1982, Cancer research.

[11]  Grace Y Sun,et al.  Prostaglandins, Fatty Acids and Phospholipids in Normal and Neoplastic Breast Tissues , 1982 .

[12]  B. Leung,et al.  Effects of 17 beta-estradiol on progesterone receptors and the uptake of thymidine in human breast cancer cell line CAMA-1. , 1981, Cancer Research.

[13]  A. Potter,et al.  Interaction of prolactin, estrogen and progesterone in a human mammary carcinoma cell line, CAMA-1 - I Cell growth and thymidine uptake. , 1981, Journal of steroid biochemistry.

[14]  H. Rochefort,et al.  A secreted glycoprotein induced by estrogen in human breast cancer cell lines , 1980, Cell.

[15]  M. Lippman,et al.  The effects of estrogens and antiestrogens on hormone-responsive human breast cancer in long-term tissue culture. , 1976, Cancer research.

[16]  A. Pardee,et al.  A restriction point for control of normal animal cell proliferation. , 1974, Proceedings of the National Academy of Sciences of the United States of America.