首页 | 本学科首页   官方微博 | 高级检索  
检索        

癌性胸腔积液端粒酶活性的检测
引用本文:严玉兰,郑金旭,王绪,汪毅,杨剑影.癌性胸腔积液端粒酶活性的检测[J].江苏大学学报(医学版),2002,12(2):146-147.
作者姓名:严玉兰  郑金旭  王绪  汪毅  杨剑影
作者单位:1. 江苏大学附属医院呼吸内科,江苏,镇江,212001
2. 徐州医学院影像系,江苏,徐州,221002
摘    要:目的:探讨端粒酶活性水平检测对癌性胸腔积液的诊断价值。方法:采用Telomerase-PCR-ELISA法检测了30例癌性胸腔积液及21例良性胸腔积液的端粒酶活性水平,并与细胞学检查比较结果:癌性胸腔积液端粒酶活性阳性率76.6%,结核性胸腔积液20%(3/15),其他病因胸腔积液0%(0/6),癌性胸腔积液端粒酶活性高于细胞学检查率36.6%(P<0.005),两者平行试验阳性率83.3%。结论:端粒酶活性的检测可能成为诊断癌性胸腔积液的重要辅助手段。

关 键 词:肿瘤  胸腔积液  端粒酶
文章编号:1006-7655(2002)02-0146-02
修稿时间:2002年1月14日

Detection of Telomerase Activity in Pleural Effusion Cells from Patients with Malignant Neoplasm
YAN Yu-lan,ZHENG Jin-xu,WANG Xu,WANG Yi,YANG Jiang-yeng.Detection of Telomerase Activity in Pleural Effusion Cells from Patients with Malignant Neoplasm[J].Journal of Jiangsu University Medicine Edition,2002,12(2):146-147.
Authors:YAN Yu-lan  ZHENG Jin-xu  WANG Xu  WANG Yi  YANG Jiang-yeng
Abstract:Objective:To investigate the diagnostic significance of the detection of telomerase activity in pleural effusion cells from patients with malignant neoplasm. Methods:The technique telomerase polymerase chain reaction(PCR)-enzyme-linked immunosorbent assay (ELISA) was employed to detect telomerase activity in 30 samples of pleural effusion cells of patients with malignant neoplasm, 20 samples of tuberculotic patients and 6 samples of patients with other diseases. Results:It was found that the positive rate of telomerase activity in samples from patients with malignant diseases were higher (76.6%) than that from tuberculotic patients(20%) or other patients(0%). The positive rate of telomerase activity in samples from patients with malignant diseases was much higher than that of cytologic measure. The combining positive rate of the two examinations was 83.3%. Conclusions:Detection of telomerase activity in pleural effusion cells would be helpful to the cytologic measure in diagnosis of patients with malignant neoplasm.
Keywords:Lung neoplasm  Pleural effusion  Telomerase
本文献已被 CNKI 维普 万方数据 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