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Subcellular Distribution of Androgen Receptors in Human Normal, Benign Hyperplastic, and Malignant Prostatic Tissues: Characterization of Nuclear Salt-resistant Receptors¹

The James Buchanan Brady Urological Institute, The Johns Hopkins Hospital [E. R. B., P. B., P. C. W.], and The Department of Urology, The Johns Hopkins University School of Medicine [E. R. B., P. B., P. C. W.], Baltimore, Maryland 21205

Two populations of nuclear androgen receptors have been characterized in human prostatic tissue, and the levels and proportions of each were found to differ in normal prostates, benign hyperplastic prostates (BPH), and malignant prostates. A significant percentage (35 to 50%) of total nuclear androgen receptors was associated with the salt-resistant nuclear matrix fraction. The remainder were easily extracted from nuclei by 0.6 M KCI. Optimal conditions for measuring receptors in both compartments involved the use of an inhibitor of proteolysis (phenylmethylsulfonyl fluoride) and the omission of dithiothreitol from buffers. In the presence of dithiothreitol, most of the nuclear salt-resistant receptors were rendered salt extractable. Cytosol androgen receptor levels were not significantly different in normal, BPH, or malignant prostatic tissues. In contrast, the levels and distribution of nuclear salt-extractable and salt-resistant androgen receptors exhibited characteristic patterns. Compared to normal prostatic tissue, nuclear salt-extractable receptors were significantly elevated in both BPH and cancer, whereas nuclear salt-resistant receptors were elevated in BPH but not in cancer. The ratio of salt-extractable to salt-resistant receptors was approximately 1:1 in both normal and BPH tissues and 2:1 in cancer. In addition, a microassay has been developed for the measurement of androgen receptors in the three subcellular compartments of needle biopsy specimens of prostatic cancer. Studies are in progress to determine whether the measurement of both nuclear salt-extractable and salt-resistant receptors may improve the usefulness of receptor levels to predict the hormonal responsiveness of prostatic cancer.

¹ Supported by Grant CA-16924 from the National Cancer Institute and Grants AM 19300 and AM 22000 from the National Institute of Arthritis, Metabolism and Digestive Diseases, NIH.

² To whom requests for reprints should be addressed, at The Brady Urological Institute, Marburg 115, The Johns Hopkins Hospital, 600 North Wolfe Street, Baltimore, Md. 21205.

Received 7/30/82. Accepted 11/23/82.

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