检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]中国科学院上海生物化学研究所分子生物学国家重点实验室
出 处:《现代妇产科进展》1996年第4期321-323,共3页Progress in Obstetrics and Gynecology
摘 要:目的:建立一种比葡聚糖活性炭(DCC)法更灵敏、准确、简便的羟基磷灰石(HAP)法测定雌激素受体(ER)的含量。方法:以SD雌性大鼠子宫胞浆抽提液为材料,用HAP法多点饱和分析和单点饱和分析ER含量;比较在测定反应中总蛋白量对HAP法和DCC法测定值的影响,并比较两者在30例乳腺癌和30例子宫肌瘤中ER测定值的差异。结果:大鼠子宫胞浆ER含量为135fmol/mg蛋白,Kd=0.58nM。当测定反应中总蛋白量低于200μg时,DCC法测定值严重失真,而HAP法在总蛋白量为50μg时仍能准确测出真实值。在30例乳腺癌和30例子宫肌瘤ER测定值中,当ER含量较低时,DCC法测定值偏低甚至有假阴性.而ER含量高时两者接近。在ER含量较高时,两者测定值相近。结论:HAP法比DCC法灵敏、可靠。用以测定甾体激素高非特异性结合的靶组织与非靶组织中的ER低含量时,HAP法更有价值。Objective To establish HAP assay a powerful method to determine estrogen receptor more sensitively,more accurately and more conveniently than that of DCC assay. Methods Uterine cytosol extracts from SD female rats were used to establish the HAP multi point saturation assay and HAP single point saturation assay.The authors examined the effect of total protein level on HAP and DCC assays and compared the ER values measured by HAP and DCC in 30 breast cancer cases and 30 leiomyoma cases respectively. Results The ER value in rat uterine cytosol extract was 135 fmol/mg cytosol protein.Kd value was 0.58nM.HAP assay could exactly determine ER value when total protein was less than 50μg,but DCC assay could not determine even when total protein level was less than 200μg.When ER level in 30 breast cancer cases and 30 leiomyoma cases was low,the value examined by DCC assay was lower than its real value,but when ER level was high enough,the value measured by DCC and HAP were almost equal to each other. Conclusions HAP assay is a more sensitive,more accurate method than that of DCC assay and plays a more valuable role on determinating low ER value in all kinds of steroid target and nontarget tumor tissues with high nonspecific binding.
关 键 词:羟基磷灰石 葡聚糖活性炭 雌激素受体 测定 肿瘤
分 类 号:R730.43[医药卫生—肿瘤] Q579.130.3[医药卫生—临床医学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.145