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Stimulation of Apolipoprotein D Secretion by Steroids Coincides with Inhibition of Cell Proliferation in Human LNCaP Prostate Cancer Cells¹

Medical Research Council Group in Molecular Endocrinology, CHUL Research Center and Laval University, Quebec G1V 4G2, Canada [J. S., R. V., Y. d. L., F. L.], and Department of Surgery, Washington University School of Medicine, St. Louis, Missouri 63110 [D. E. H.]

Although steroid hormones are known to play a predominant role in the regulation of cell growth in hormone-sensitive cancers, their mechanisms of action, especially their interaction with growth factors and/or growth inhibitors, is poorly understood. We have recently observed that the effects of androgens and estrogens on the expression of the major protein found in human breast gross cystic disease fluid, protein-24, are opposite to their respective action on cell proliferation in human breast cancer cell lines. Somewhat surprisingly, the recent elucidation of the amino acid sequence of this progesterone binding protein reveals that this tumor marker is apolipoprotein D (apo D), a member of a superfamily of lipophilic ligand carrier proteins. The present study was designed to determine whether apo D is secreted by human prostate cancer cells and could thus be a new marker of steroid action in these cancer cells, and whether the sex steroid-induced stimulation of apo D secretion coincides with inhibition of cell proliferation. We took advantage of the biphasic pattern of the effect of steroids on the proliferation of the human prostate cancer LNCaP cell line, which offers the opportunity to discriminate between positive and negative steroid receptor-regulated cell growth processes. A 10-day exposure to low concentrations of dihydrotestosterone and testosterone caused a potent stimulation of LNCaP cell proliferation, whereas incubation with higher concentrations of these androgens led to a progressive decrease in cell proliferation towards basal levels. The biphasic action of androgens was also observed on apo D secretion, the effects on apo D secretion being inversely related to their action on LNCaP cell proliferation. Similar opposite biphasic effects were also observed with 9 other steroids, thus indicating that the stimulation of secretion of this new biochemical marker coincides with inhibition of cell proliferation in LNCaP human prostatic cancer cells.

¹ Financial support was from Pharmacia Canada and Endorecherche. J. S. is holder of a Scholarship from the Medical Research Council of Canada. Y. d. L. is holder of a postdoctoral fellowship from the Medical Research Council of Canada.

² To whom requests for reprints should be addressed, at MRC Group in Molecular Endocrinology, CHUL Research Center, 2705 Laurier Boulevard, Quebec G1V 4G2, Canada.

Received 4/24/91. Accepted 6/ 4/91.

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