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A microassay for the measurement of androgen receptors in human prostatic tissue.

作者信息

Hicks L L, Walsh P C

出版信息

Steroids. 1979 Apr;33(4):389-406. doi: 10.1016/0039-128x(79)90014-x.

DOI:10.1016/0039-128x(79)90014-x
PMID:442131
Abstract

A microassay utilizing R 1881 (methyltrienolone) has been developed for the measurement of androgen receptor sites in the cytosol and nuclear extract of human prostatic tissue. Binding of R 1881 to the progesterone binding molecule in cytosol was eliminated by the addition of triamcinolone acetonide. Utilizing a six tube, single point assay, the number of binding sites estimated in nuclear extract averaged 95% of the number measured by a full 7 point Scatchard analysis; the number estimated by the microassay in cytosol averaged 91%. When the single point assay was applied to needle biopsy specimens (200 mg of tissue), the estimated number of binding sites in nuclei averageed 83% of the number measured in bulk tissue (2 grams) utilizing a 7 point Scatchard analysis; the number in cytosol estimated by the microassay on needle biopsy specimens averaged 73%. It is hoped that this technique may be useful in correlating receptor content with hormonal responsiveness in men with metastatic carcinoma of the prostate.

摘要

相似文献

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A microassay for the measurement of androgen receptors in human prostatic tissue.
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Binding of [3H]methyltrienolone to androgen receptor in rat liver.
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[Prostatic cytoplasmic androgen receptor in prostatic disease. I. Serum androgen levels, cytoplasmic androgen levels and cytoplasmic R1881 receptor in prostatic disease].
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