期刊文献+

Pak1基因在乳腺癌组织中的表达及临床意义 被引量:2

Expression of Pak1 gene in breast carcinoma and its clinical significance
下载PDF
导出
摘要 目的研究乳腺肿瘤组织中p21激活激酶1(Pak1)mRNA及其蛋白在正常乳腺组织、良性乳腺肿瘤组织、乳腺癌组织中表达的情况,探讨Pak1与淋巴结转移、雌激素受体(ER)、孕激素受体(PR)及癌胚表达抗原(CerbB-2)表达的关系。方法采用实时荧光定量RT-PCR技术检测35例乳腺癌和20例乳腺良性病变、15例远癌正常乳腺小叶组织中Pak1 mRNA的丰度表达,免疫组化法检测35例乳腺癌和20例乳腺良性病变组织标本中Pak1蛋白的过度表达阳性率,并进行相关统计分析。结果乳腺癌、乳腺良性病变和正常乳腺小叶组织中Pak1 mRNA表达量分别为4.76±0.11、2.66±0.10、0.94±0.06,各组间比较差异有统计学意义(P<0.05)。在ER阳性与ER阴性组织中,Pak1 mRNA相对表达量为5.04±0.69、4.59±0.57,二者比较差异有统计学意义(P<0.05)。35例乳腺癌组织标本中,Pak1蛋白在ER阳性与ER阴性组织中过度表达阳性率分别为90.48%(19/21)和57.14%(8/14),二者比较差异有统计学意义(P<0.05);在PR阳性与PR阴性组织中过度表达阳性率分别为86.96%(20/22)和53.85%(7/13),二者比较差异有统计学意义(P<0.05)。Pak1 mRNA相对表达量和蛋白的过度表达阳性率均与乳腺癌患者年龄、肿瘤大小、CerbB-2表达水平和淋巴结是否转移未见相关性(P>0.05)。结论 Pak1基因表达增强是乳腺癌的普遍现象,且可能与ER、PR水平有关。 Objective To investigate mRNA and protein expression of Pak1 gene in normal breast tissue,benign mammary lesions and breast carcinoma,to explore whether the expression of Pak1gene in breast carcinoma is related to lymph node metastases,the level of ER,PR and CerbB-2 or not.Methods The mRNA expression of Pak1 gene was detected in 35 cases of breast carcinoma,20 cases of benign mammary lesions and 15 cases of normal breast tissue by fluorescent real-time RT-PCR;35 cases of paraffin-embedded specimens of breast carcinoma and 20 cases of benign mammary lesions were studied by immunohistochemical assay.Statistical analysis was carried out to analyze the correlation between Pak1 gene expression and clinical significance in these breast cancer patients.Results The mRNA expressions of Pak1 gene were detected in 35 cases of breast carcinoma,20 cases of benign mammary lesions and 15 cases of normal breast tissue by fluorescent real-time RT-PCR relative expression level of Pak1 mRNA were 4.76±0.11,2.66±0.10,0.94±0.06(P0.05);the relative expression level of Pak1 mRNA in breast carcinoma with ER positive and ER negative were 5.04±0.69,4.59±0.57(P0.05);the protein expression of Pak1 was detected in 35 cases of breast careinoma and 20 cases of benign mammary lesions by immunohistochemical assay.The over expression rate of Pak1 in breast carcinoma with ER positive and ER negative were 90.48%(19/21) and 57.14%(8/14,P0.05);in breast carcinoma with PR positive and PR negative were 86.96%(20/22) and 53.85%(7/13,P0.05);neither mRNA nor protein expression of Pak1 gene was correlated with age of patients,size of tumor,the level of CerbB-2(P0.05);Conclusion Pak1 over expression is a common phenomenon in breast cancer,and may be related to the level of ER and PR of breast carcinoma.
出处 《重庆医学》 CAS CSCD 北大核心 2011年第7期646-649,I0003,共5页 Chongqing medicine
关键词 乳腺肿瘤 逆转录聚合酶链反应 免疫组织化学 p21活化激酶类 breast neoplasms reverse transcriptase polymerase chain reaction immunohistochemistry p21-activated kinases
  • 相关文献

参考文献14

  • 1Bagheri-Yarmand R,Mandal M,Taludker AH,et al.Etk/Bmx tyrosine kinase activates Pak1 and regulates tumorigenicity of breast cancer cells[J].J Biol Chem,2001,276(31):29403-29409.
  • 2Livak KJ,Schmittgen TD.Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method[J].Methods,2001,25(4):402-408.
  • 3Eeienne-Manneille S,Hau A.RhoGTPase in Cell biology[J].Nature,2002,420(7):620-635.
  • 4Bokoch GM.Biology of the p21-activated kinases[J].Annu Rev Biochem,2003,72:743-81.
  • 5Carter JH,Douglass LE,Deddens JA,et al.Pak-1 expression increases with progression of colorectal carcinomas to metastasis[J].Clin Cancer Res,2004,10(10):3448-3456.
  • 6Mazumdar A,Kumar R.Estrogen regulation of Pak1 and FKHR pathways in breast cancer cells[J].FEBS Lett,2003,535(1-3):6-10.
  • 7Coniglio SJ,Zavarella S,Symons MH.Pak1 and Pak2 mediate tumor cell invasion through distinct signaling mechanisms[J].Mol Cell Biol,2008,28(12):4162-4172.
  • 8Chau CH,Chen KY,Deng HT,et al.Coordinating Etk/Bmx activation and VEGF upregulation to promote cell survival and proliferation[J].Oncogene,2002,21(57):8817-8829.
  • 9Molli PR,Li DQ,Murray BW,et al.PAK signaling in oncogenesis[J].Oncogene,2009,28(28):2545-2555.
  • 10罗勇军,刘昕.实时荧光定量PCR标准品的制备及应用[J].重庆医学,2005,34(3):414-415. 被引量:37

二级参考文献1

  • 1张鋆.荧光实时定量PCR技术初探[J].生命科学趋势,2003,12(1):1-28.

共引文献36

同被引文献15

引证文献2

二级引证文献6

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