首页 | 本学科首页   官方微博 | 高级检索  
     

应用化学发光酶免疫法测定妇科肿瘤组织雌激素受体
引用本文:顾美皎 周宜开. 应用化学发光酶免疫法测定妇科肿瘤组织雌激素受体[J]. 中华妇产科杂志, 1994, 29(9): 531-534
作者姓名:顾美皎 周宜开
作者单位:同济医科大学附属同济医院妇产科,同济医科大学环境医学研究所
摘    要:为了寻找一种理想的性激素受体的检测方法,本研究首先应用化学发光酶免疫法(CLEIA)测定34例妇科肿瘤(子宫内膜癌15例、卵巢肿瘤15例及其他肿瘤4例)组织的雌激素受体(ER),并与葡聚糖包裹活性碳法(DCC)及酶免疫测定法(EIA)进行对照。结果:(1)CLEIA标准曲线显示发光强度和ER浓度线性关系良好(r=0.9786)。(2)CLEIA测得ER值与DCC或EIA所测ER值的相关性极显著(P<0.001),相符率>90%。(3)三种方法测得的ER阳性率,差异无显著性,而ER均值以CLEIA为最高。结论:CLEIA测定ER的敏感性较另两法为高。

关 键 词:化学发光酶免疫法,雌激素受体,生殖器肿瘤,女性

A controlled study of chemiluminescent enzymeimmunoassay for the measurement of estrogenreceptor in tissue of gynecological neoplasms
.Gu MeiJiao, Zhou Yikai, Zheng Wen,et al.. A controlled study of chemiluminescent enzymeimmunoassay for the measurement of estrogenreceptor in tissue of gynecological neoplasms[J]. Chinese Journal of Obstetrics and Gynecology, 1994, 29(9): 531-534
Authors:.Gu MeiJiao   Zhou Yikai   Zheng Wen  et al.
Abstract:n this study, chemiluminescent enzyme im-munoassay (CLEIA) has been developed for the mea-surement of estrogen receptor (ER) in 34 gynecologicaloncological tissues from 15 cases of endometrial carci-noma, 15 cases of ovarian tumors and 4 cases of othergynecological tumors. The accuracy , specificity and sen-sitivity of CLEIA for ER were compared with that ofdextrancoated charcoal (DCC) and enzyme immunoas-say (EIA).Results: (1) the standard curve of ER-CLEIAshowed a significant llnear correlation between the lumi-nosity and ER concentration (r=0. 9786 , P<0. 001);( 2) The results of CLEIA and that of the other twomethods were compared; the correlation coefficientswere>0. 8 and their corresponding rates were>90%;; (3)the positive rate of ER determind by these threemethods showed no significant differences, however,the mean value of ER-CLEIA was the highest amongthem.It is concluded that the CLEIA has a higher sensi-tivity than that of the other two methods for the mea-surement of ER.
Keywords:Chemiluminescent enzyme im-munoassay Estrogen receptor Genital neo-plasms    female
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号