Kohigashi K, Fukuda Y, Imura H
Gastroenterol Jpn. 1987 Jun;22(3):322-30. doi: 10.1007/BF02774258.
Specimens of human liver obtained at the time of operation were assayed for cytosolic estrogen receptors by the binding assay and enzyme immunoassay (EIA). Mean estrogen receptor contents determined by the binding assay were 17.8 fmol/mg protein in non-cirrhotic liver, 7.1 in cirrhotic liver, and 0.7 in hepatocellular carcinoma, by EIA the contents were 12.1, 5.9, and 0.8 fmol/mg protein, respectively. There were significant differences among the three groups. In particular, hepatocellular carcinoma specimens contained very little or no detectable amounts of estrogen receptors in either assay. The correlation between the estrogen receptor content determined by the binding assay and that determined by EIA was significant (r = 0.822, p less than 0.001). It is suggested that the estrogen receptor content decreases with the development of liver cirrhosis and hepatocellular carcinoma and that antiestrogen endocrine therapy for hepatocellular carcinoma may be ineffective.
通过结合分析法和酶免疫分析法(EIA)对手术时获取的人体肝脏标本进行细胞溶质雌激素受体检测。结合分析法测定的非肝硬化肝脏中雌激素受体平均含量为17.8 fmol/mg蛋白质,肝硬化肝脏中为7.1,肝细胞癌中为0.7;EIA法测定的含量分别为12.1、5.9和0.8 fmol/mg蛋白质。三组之间存在显著差异。特别是,在两种检测方法中,肝细胞癌标本所含雌激素受体极少或检测不到。结合分析法测定的雌激素受体含量与EIA法测定的含量之间存在显著相关性(r = 0.822,p < 0.001)。提示雌激素受体含量随肝硬化和肝细胞癌的发展而降低,肝细胞癌的抗雌激素内分泌治疗可能无效。