首页 | 本学科首页   官方微博 | 高级检索  
     

PCNA在前列腺癌及良性前列腺增生症组织中的表达及其临床意义
引用本文:胡广平,毕学成,何慧婵,叶永康,韩兆冬,梁宇翔,钟惟德. PCNA在前列腺癌及良性前列腺增生症组织中的表达及其临床意义[J]. 岭南现代临床外科, 2008, 8(4): 285-286
作者姓名:胡广平  毕学成  何慧婵  叶永康  韩兆冬  梁宇翔  钟惟德
作者单位:广东省乳源县人民医院外科,512700;广东省广州市第一人民医院泌尿外科,510180
摘    要:
目的探讨PCNA存前列腺癌及良性前列腺增生症组织中的表达及其在诊断前列腺癌的临床意义。方法运用实时荧光定量PCR方法检测40例前列腺癌病理组织以及良性前列腺增生症组织的PCNA的基冈表达水平。结果PCNA在前列腺癌组织中表达值为9.23±0.55,在良性前列腺增生症组织中表达值为1.23±0.04,前列腺癌中PCNA表达值高于良性前列腺增生症组织,差异有显著性(P〈0.01)。结论前列腺癌组织中PCNA基斟呈现为高表达,它有助于对前列腺癌的诊断。

关 键 词:实时荧光定量PCR  前列腺癌  良性前列腺增生症  增殖细胞核抗原

Expression of PCNA in prostatic carcinoma and BPH tissue and its clinical value
HU Guangpin,BI Xuecheng,HE Huichan,YE Yongkang,HAN Zhaodong,LIANG Yuxiang,ZHONG Weide. Expression of PCNA in prostatic carcinoma and BPH tissue and its clinical value[J]. Lingnan Modern Clinics in Surgery, 2008, 8(4): 285-286
Authors:HU Guangpin  BI Xuecheng  HE Huichan  YE Yongkang  HAN Zhaodong  LIANG Yuxiang  ZHONG Weide
Affiliation:HU Guangpin ,BI Xuecheng,HE Huichan, YE Yongkang,HAN Zhaodong,ZHONG Weide ( 1.Department of Surgery, Ruyuan Xian People's Hospital, Guangdong 512700; 2. Department of Urology, The First people's Hospital of Guangzhou 510080)
Abstract:
Objective To study the PCNA mRNA expression in prostatic carcinoma(PCa) and BPH tissue by real-time fluorescence quantitative PCR and its clinical value for diagnosing cancer of prostate. Methods A real-time quantitative PCR assay was used to detect the level of PCNA gene expressions in 40 cases with cancer of prostate and 45 cases with benign prostate hyperplasia tissue. Results The expression level of PCNA in PCa and BPH tissue were 9.23±0.55, and 1.23±0.04 respectively and there were significant difference between two groups (P〈0.01). Conclusion In the tissue of cancer of prostate,PCNA gene shows a high expression. It would contribute to diagnose the cancer of prostate.
Keywords:Real-time fluorescence quantitative PCR  Cancer of prostate  Benign prostatic hyperplasia  Proliferating cell nuclear antigen (PCNA)
本文献已被 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