Sex steroid binding patterns in primary biliary cirrhosis complicated by hepatocellular carcinoma.

Owing to recent findings of certain unusual sex steroid binding in liver disease--particularly an allosteric biphasic pattern (pattern A) unique to the serum of patients with hepatocellular carcinoma--the serum binding characteristics for 5 alpha-dihydrotestosterone were examined in serum samples from six patients with primary biliary cirrhosis who had developed hepatocellular carcinoma. In all serum samples taken after the development of tumour pattern A binding only was obtained, and in four cases in which earlier samples were also examined there was a transformation from the normal, non-specific binding pattern, or an allosteric plateau pattern seen in non-malignant liver disease (designated D and C respectively), to pattern A coincident with the rise in serum alpha fetoprotein. In one patient chemotherapy leading to a fall in alpha fetoprotein abolished pattern A binding, showing further its close association with tumour growth. The value of pattern A binding as a tumour marker in hepatocellular carcinoma warrants further study.

[1]  J. Neuberger,et al.  Hepatocellular carcinoma in primary biliary cirrhosis: detection by alpha-fetoprotein estimation. , 1984, Gastroenterology.

[2]  P. Johnson,et al.  Sex steroid receptor proteins in foetal, adult and malignant human liver tissue. , 1983, British Journal of Cancer.

[3]  M. Soloff,et al.  Oxytocin receptors and parturition. I. Control of oxytocin receptor concentration in the rat myometrium at term. , 1980, Endocrinology.

[4]  R. N. Macsween,et al.  Hepatocellular carcinoma in primary biliary cirrhosis: report of four cases. , 1979, Gut.

[5]  M. Iqbal,et al.  Study of steroid-protein binding by a novel "two-tier" column employing Cibacron Blue F3G-A-Sepharose 4B. I-Sex hormone binding globulin. , 1977, Journal of steroid biochemistry.

[6]  M. Soloff,et al.  The Lack of Estrogen Binding by Human α-Fetoprotein1 , 1974 .

[7]  E. Jensen,et al.  THE DEPRESSION OF ESTRONE-INDUCED UTERINE GROWTH BY PHENOLIC ESTROGENS WITH OXYGENATED FUNCTIONS AT POSITIONS 6 OR 16: THE IMPEDED ESTROGENS , 1955, The Journal of experimental medicine.

[8]  J. Thijssen,et al.  In vivo uptake and subcellular distribution of tritium-labeled estrogens in human endometrium, myometrium, and vagina. , 1983, The Journal of clinical endocrinology and metabolism.

[9]  E. W. Bergink Oestriol receptor interactions: their biological importance and therapeutic implications. , 1980, Acta endocrinologica. Supplementum.

[10]  P. Insel,et al.  alpha Adrenoreceptors but not beta adrenoreceptors increase in rabbit uterus with oestrogen. , 1977, Nature.

[11]  J. H. Clark,et al.  Estrogen-induced uterine responses and growth: relationship to receptor estrogen binding by uterine nuclei. , 1975, Endocrinology.

[12]  M. Soloff,et al.  The lack of estrogen binding by human alpha-fetoprotein. , 1974, The Journal of clinical endocrinology and metabolism.

[13]  P. Siiteri,et al.  Placental estrogen biosynthesis during human pregnancy. , 1966, The Journal of clinical endocrinology and metabolism.