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乳腺癌组织中E-cadherin的表达与外周血微转移的相关性及临床意义 被引量:3

Expression and significance of E-cadherin in benign and malignant mammary tumor .
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摘要 目的检测乳腺癌组织中E-cadherin的表达及患者外周血微转移的发生,探讨二者的相互关系及临床意义。方法应用逆转录-聚合酶链反应(RT-PCR)分别检测15例乳腺良性肿瘤患者及60例乳腺癌患者外周血CK-20及乳腺组织中E-cadherin mRNA的表达。结果15例乳腺良性肿瘤组织中,均有E-cadherin阳性表达(100%),而60例乳腺癌组织中,E-cadherin阳性表达23例(38.3%),二者差异显著(P<0.01);CK-20在乳腺良性肿瘤患者外周血中未见表达。在60例乳腺癌患者外周血中,检出CK-20阳性表达28例(46.7%),E-cadherin在相应癌组织中的阳性表达率为14.3%(4/28),32例外周血CK-20阴性的乳腺癌病例中,E-cadherin的阳性表达率为59.3%(19/32),二者差异显著(P<0.01)。结论乳腺癌组织中E-cadherin的低表达与外周血高转移率显著相关,提示E-cadherin的表达缺失或低表达可能是导致乳腺癌高转移的因素之一,可作为临床判断预后的参考指标。 Objective To explore the expression of E - cadherin in mammary tumor and its clinical significance as well as the relationship with the circulating tumor cell in blood of the breast cancer patients. Methods E - cadherin mRNA in 15 cases of benign breast disease and 40 cases of breast cancer were detected by reverse transcriptase -polymerase chain reaction( RT -PCR). CK20 mRNA was also detected by RT -PCR in blood as an index of circulating tumor cells in breast cancer patients. Results Positive rates of E - cadhefin in benign breast disease and breast cancer were 100% and 38. 3% , respectively. There was static significance between the two groups ( P 〈 0.01),CK20 mRNA was not detected in blood of patients with benign breast disease,In breast cancer patients,the positive rate was 46.7%,Positive rate of E-cadherin in breast cancer patients with CK20 positive disease and negative disease were 14.3%(4/28/)and 59.3%(19/32/),respectively,There was a significant difference between the two groups(P〈0.01),Conclusion Aberrant expression of E-cadherin was closely related with the development of blood metastasis in breast cancer.The expressed deficiency or low expression of E-cadherin may be one of the factors responsible for the high metastasis.It may be a prognostic maker of breast cancer.
出处 《现代肿瘤医学》 CAS 2005年第6期758-760,共3页 Journal of Modern Oncology
关键词 E-CADHERIN 乳腺肿瘤 转移 E-cadherin mammary neoplasm metastasis
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  • 1Albelda SM. Role of integrins and other cell adhesion molecules in tumor progression and metastasis[J]. Lab Invest,1993, 68(1):4~17.
  • 2Charalabopoulos K, Gogali A, Kostoula OK, et al. Cadherin superfamily of adhesion molecules in primary lung cancer[J]. Exp Oncol, 2004, 26(4): 256~260.
  • 3Khoursheed MA, Mathew TC, Makar RR, et al. Expression of E-cadherin in human colorectal cancer[J]. Surgeon, 2003, 1(2): 86~91.
  • 4Takeichi M. Cadherin cell adhesion receptors as a morphogenetic regulator[J]. Science,1991, 251(5000):1451~1455.
  • 5Behrens J, Mareel MM, Van Roy FM, et al. Dissecting tumor cell invasion: epithelial cells acquire invasive properties after the loss of uvomorulin-mediated cell-cell adhesion[J]. J Cell Biol, 1989,108(6): 2435~2447.
  • 6Reynolds AB, Carnahan RH. Regulation of cadherin stability and turnover by p120ctn: implications in disease and cancer[J]. Semin Cell Dev Biol, 2004 , 15(6):657~663.
  • 7Mell LK, Meyer JJ, Tretiakova M, et al. Prognostic significance of E-cadherin protein expression in pathological stage I-III endometrial cancer[J]. Clin Cancer Res, 2004,10(16):5546~5553.
  • 8Kudo Y, Kitajima S, Ogawa I, et al. Invasion and metastasis of oral cancer cells require methylation of E-cadherin and/or degradation of membranous beta-catenin[J]. Clin Cancer Res, 2004,10(16):5455~5463.
  • 9Moersig W, Horn S, Hilker M, et al. Transfection of E-cadherin cDNA in human lung tumor cells reduces invasive potential of tumors[J]. Thorac Cardiovasc Surg, 2002,50(1):45~48.
  • 10Datta YH, Adams PT, Drobyski WR, et al.Sensitive detection of occult breast cancer by the reverse-transcriptase polymerase chain reaction[J]. J Clin Oncol, 1994,12(3):475~482.

同被引文献47

  • 1周永宁,徐采朴,韩彪,姬瑞.胃癌E-cadherin基因启动子CpG岛甲基化的研究[J].癌症,2005,24(10):1220-1224. 被引量:9
  • 2Braun S,Pantel K,Muller P,et al.Cytokeratin-positive cells inthe bone marrow and survival of patients with stage I,II,or IIIbreast cancer[J].N Engl J Med,2000,342:525-533.
  • 3Husemann Y,Creigi BJ,Schubert,et al.Systemic spread is anearly step in breast cancer[J].Cancer Cell,2008,13:58-68.
  • 4Datta YH,Adams PT,Drobyski WR,et al.Sensitive detection of occult breast cancer by the reverse-transcriptase polymerase chainreaction[J].J Clin Oncol,1994,12(3):475-482.
  • 5Krishnamurthy S,Cristofanilli M,Singh B,et al.Detection of minimal residual disease in blood and bone marrow in early stagebreast cancer[J].Cancer,2010,116(14):3330-3337.
  • 6Gilje B,Nordgrd O,Tjensvoll K,et al.Mitotic activity and bonemarrow micrometastases have independent prognostic value in nodepositive breast cancer patients.Breast[J].Cancer Res Treat,2011,128(1):137-146.
  • 7SoláM,MargelíM,CastelláE,et al.Prognostic value of hema-togenous dissemination and biological profile of the tumor in earlybreast cancer patients:A prospective observational study[J].BMCCancer,2011,11:252.
  • 8Bozionellou V,Mavroudis D,Perraki M,et al.Trastuzumab ad-ministration can effectively target chemotherapy-resistant cytoker-atin-19 messenger RNA-positive tumor cells in the peripheralblood and bone marrow of patients with breast cancer[J].ClinCancer Res,2004,10(24):8185-8194.
  • 9Rack B,Jückstock J,Günthner-Biller M,et al.Trastuzumab clears HER2/neu-positive isolated tumor cells from bone marrowin primary breast cancer patients[J].Arch Gynecol Obstet,2011,6:30.
  • 10Herzig M, Savarese F, Novatehkova M, et al. Tumor progression induced by the loss of E - cadherin independent of beta - catenin/ Tcf- mediated Wnt signaling [J]. Oncogene, 2007, 26 (16) : 2290 - 2298.

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