期刊文献+

DELFIA检测血清PSA、fPSA及fPSA/PSA在前列腺疾病诊断中的应用 被引量:5

Application of serum PSA, fPSA detections and fPSA/PSA evaluation for diagnosis and therapy of prostatic diseases with DELFIA technique
下载PDF
导出
摘要 目的:探讨双标记时间分辨荧光免疫分析(DELFIA)检测血清PSA、fPSA及fPSA/PSA在前列腺疾病诊断中的应用。方法:应用DELFIA法检测正常对照组(34例)、前列腺炎组(46例)、前列腺增生症组(123例)及前列腺癌组(39例)血清PSA、fPSA含量及fPSA/PSA。结果:前列腺癌组PSA、fPSA与其他三组比较差异均有显著性(P<0·01),而其他3组之间比较差异显著性(P>0·05);前列腺癌组fPSA/PSA明显降低,与其他3组比较差异均有显著性(P<0·05)。结论:应用DELFIA检测PSA、fPSA含量及fPSA/PSA是提高前列腺疾病诊断与鉴别诊断更为有效的方法,尤其对前列腺癌诊断更有意义。 Objective To investigate the application of PSA, fPSA concentrations and fPSA/PSA value for diagnosis and therapy of prostatic diseases detected with dissociation enhanced lautbanide fluoroimmunoassay (DELFIA) technique. Methods Thirty-four cases of normal individuals were used as control group, 46 patients with prostatitis as prostatitis group, 123 patients with prostatic hyperplasia as BPH group and 39 patients with prostate cancer as prostate cancer group. PSA, fPSA concentrations and fPSA/PSA value were detected with DELFIA technique. Results In prostate cancer group, the PSA and fPSA concentrations were significantly higher than those in other 3 groups (P〈0.01), as fPSA/PSA value was remarkably lower than those in the other 3 groups (P〈0.05). However, the fPSA/PSA values in other 3 groups demonstrated no significant difference (P 〉 0.05 ). Conclusion DELFIA technique is an effective method to improve the diagnosis and differential diagnosis of prostatic diseases, especially for prostate cancer.
出处 《吉林大学学报(医学版)》 CAS CSCD 北大核心 2006年第5期851-853,共3页 Journal of Jilin University:Medicine Edition
基金 教育部留学回国科研启动基金资助课题[(2003)科技学(164)号]
关键词 DELFIA 前列腺肿瘤 PSA fPSA、fPSA/PSA DELFIA prostatic neoplasms PSA fPSA fPSA/PSA
  • 相关文献

参考文献8

二级参考文献50

  • 1王寅 黄长海 等.前列腺特异抗原不同评价结果与前列腺癌的关系分析[J].中华医学杂志,2000,80(9):678-680.
  • 2Borgono CA,Michael IP,Diamandis EP.Human tissue kalliikreins:physiologic roles and applications in caner. Mol Cancer Res,2004,2(5) :257 -80.
  • 3Yousef GM, Diamandis EP. Expanded human tissue kallikrein family - a novel panel of cancer biomarkers. Tumour Biol,2002,23(3): 185 - 92.
  • 4Stephen D, Mikolajczyk, Harry G. Pro PSA:a more cancer specific form of prostate specific antigen for the early detection of prostate cancer. Keio J Med,2003,52(2) :86 - 91.
  • 5Henrique R, Jeronimo C.Molecular Detection of Prostate Cancer. A Role for G STP1 Hypermethylation. Eur Urol,2004,46(5) :660 - 669.
  • 6Li LC,Okino ST,Dahiya R.DNA methylation in prostate cancer. Biochim Biophys Acta,2004,1704(2) :87- 102.
  • 7Lee WH,Morton RA, Epstein JI,et al. Cytidine methylation of regulatory sequences near the pi - class glutathione S - transferase gene accompanies human prostatic carcinogenesis. Proc Natl Acad Sci USA, 1994,91 (24):11733 - 7.
  • 8Nakayarna M, Bennett CJ, Hicks JL, et al. Hypermethylation of the human glutathione S - transferase - pi gene (GSTP1) CpG island is present in a subset of proliferative inflammatory atrophy lesions but not in normal or hyperplasfc epithelium ofthe prostate: a detailed study using laser- capture microdissection. Am J Pathol, 2003,163(3) :923 - 33.
  • 9Goessl C, Muller M, Heicappell R, et al. DNA - based detection of prostate cancer in urine after prostatic msssage. Urology, 2001,58 (3):335 - 8.
  • 10Cairns P, Esteller M, Herman JG, et al. Molecular detection of prostate cancer in urine by G STP1 hypermethylation. Clin Cancer Res, 2001,7(9) :2727 - 30.

共引文献53

同被引文献29

引证文献5

二级引证文献22

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部