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前列腺癌与前列腺增生Ki-67/PCNA mRNA特异性表达比值的研究 被引量:2

Ratio of Ki-67/PCNA mRNA and its application in the diagnosis of BHP and prostate cancer
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摘要 目的以实时荧光定量RT-PCR技术研究良性前列腺增生(BPH)与前列腺癌(PCa)组织标本Ki-67蛋白和组织核增殖抗原(PCNA)mRNA的比值,探讨此比值在PCa诊断中的特异性意义。方法通过实时荧光定量RT-PCR检测63例PCa和37例BPH前列腺组织Ki-67/PCNAmRNA的表达,比较其在PCa与BPH组织中定量的差异。结果BPH与PCa组织Ki-67/PC-NA mRNA的定量表达值分别为2.264±0.460与5.905±0.780,差异有统计学意义(P<0.05)。结论实时荧光定量RT-PCR检测Ki-67/PCNA mRNA为PCa的诊断提供了可靠的辅助指标。 Objective To study the ratio of Ki-67/PCNA mRNA and explore its application in the diagnosis of BPH and PCa. Methods A sensitive, real-time quantitative PCR assay was used to compare the expression difference of Ki-67/PCNA mRNA in BPH, PCa prostate tissue. Totally 63 samples of PCa and 37 BHP were studied. Results The ratio of Ki-67/PCNA mRNA in BPH and PCa prostate tissue is 2. 264±0. 460 and 5. 905±0. 780 respectively (P〈0. 05). Conclusions The detection result of Ki-67/PCNA mRNA expression by QRT-PCR may provide reliable diagnostic information for differential diagnosis of PCa.
出处 《现代泌尿生殖肿瘤杂志》 2009年第1期28-31,共4页 Journal of Contemporary Urologic and Reproductive Oncology
基金 国家自然科学基金资助项目(30872960) 国家高科技863资助项目(2006AA02A245) 广东省自然科学基金资助项目(04003650)
关键词 前列腺肿瘤 基因表达 实时荧光定量RT-PCR Ki-67/PCNA Prostatic neoplasms Gene expression Real-time quantitative RT-PCR Ki-67/PCNA
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  • 1董昌元,王玲,王贤明,易建华,姚启盛.前列腺癌组织中PCNA、MVD表达与彩超血流检测的研究[J].中国临床医学影像杂志,2007,18(1):56-58. 被引量:2
  • 2冯晓莉.泌尿系统及男性生殖器官肿瘤病理学和遗传学[M].北京:人民卫生出版社.2006:176.
  • 3Mousses S, Bubendorf L,Waqner U,et al. Clinical validation ofcandidate genes associated with prostate cancer progression in theCWR22 model system using tissue microarrays[ J]. Cancer Res,2002,62(5):1256 -60.
  • 4Basu G D,Azorsa D 0,Kiefer J A, et al. Functional evidenceimplicating S100P in prostate cancer progression [ J ]. Int J Canc-er, 2008,123(2) :330 -9.
  • 5Logsdon C D,Simeone D M,Binkley C,et al. Molecular profilingof pancreatic adenocarcinoma and chronic pancreatitis identifiesmultiple genes differentially regulated in pancreatic cancer [ J ].Cancer Res, 2003,63(12) :2649 -57.
  • 6Diederichs S, Bulk E, Steffen B, et al. S-100 family membersand trypsinogens are predictors of distant metastasis and survival inearly-stage non-small cell lung cancer[J]. Cancer Res, 2004,64(16):5564 -9.
  • 7Fuentes M K, Nigavekars S, Arumgam T, et al. RAGE activationby S100P in colon cancer stimulates growth, migration, and cellsignaling pathways[ J]. Dis Colon Rectum, 2007,50(8) :1230 -40.
  • 8Higgins J P, Kaygusuz G,Wang L,et al. Placental S100(S100P) and GATA3 : markers for transitional epithelium andurothelial carcinoma discovered by complementary DNA microarray[J]. Am J Surg Pathol, 2007,31(5) :673 -80.
  • 9Fuentes M K, Nigavekars S, Arumgam T, et al. RAGE activationby SlOOp in colon cancer stimulates growth, migration, and cellsignaling pathways[ J]. Dis Colon Rectum, 2007,50(8) :1230 -40.
  • 10Schmidt M H, Broil R, Bruch HP,et al. The proliferation mark-er pKi-67 organizes the nucleolus during the cell cycle dependingon Ran and cyclin B[J]. J Pathol, 2003 ,199( 1) : 18 -27.

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