[糖皮质激素受体的激活能力,作为人类肿瘤激素敏感性的可能标准]。

Eksperimental'naia onkologiia Pub Date : 1990-01-01
E S Gershteĭn, K D Smirnova, L S Bassalyk
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引用次数: 0

摘要

为评价糖皮质激素受体(GR)的功能活性,建立了在大鼠肝脏实验模型上测定其活性形态的方法。该方法是基于GR与dna -纤维素的相互作用。研究表明,大鼠肝脏总GR的26-41%能够被激活并与dna -纤维素结合。在88例肾肿瘤和37例黑色素瘤中研究了活化GR。20%的肾肿瘤和33%的黑色素瘤含有不能被激活的GR。在大多数情况下,激活的GR数远低于GR总数。总GR浓度与活化GR浓度之间无直接关系,总GR含量与整个受体池中活化形式的百分比之间无直接关系。研究活化GR可能比测定总受体含量提供更可靠的肿瘤激素敏感性信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The capacity of glucocorticoid receptors for activation as a possible criterion of the hormonal sensitivity of human tumors].

For the functional activity evaluation of glucocorticoid receptors (GR) a specific method for their activated form determination was developed on the experimental model of the rat liver. The method is based on the interaction of GR with DNA-cellulose. It has been shown that 26-41% of the total rat liver GR are able of undergoing activation and being bound to DNA-cellulose. Activated GR were studied in 88 renal tumours and in 37 melanomas. 20% of renal tumours and 33% of melanomas contain GR which are not able to undergo activation. The number of activated GR in most cases is much lower than the total GR number. There is no direct correlation between the concentrations of total and activated GR, as well as between the total GR content and the percent of activated forms in the whole receptor pool. It appears that the study of activated GR may give more reliable information about the hormone sensitivity of tumours than the determination of the total receptor content.

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