文模板,文格式样本

点赞:5125 浏览:19821 近期更新时间:2024-03-25 作者:网友分享原创网站原创

论文格式样本

退修稿:稿号

肾透明细胞癌中血管内皮生长因子表达及微血管密度的临床病理研究

鲁海珍冯晓莉孙耘田应建明陈雁石素胜刘秀云(

[摘 要]目的探讨肾透明细胞癌中血管内皮生长因子(VEGF)表达及微血管密度(MVD)的临床病理意义.方法应用免疫组织化学方法检测VEGF蛋白表达,通过CD34抗体标记血管内皮来计算MVD值.结果66例肾透明细胞癌VEGF蛋白表达阳性率为54.5%(36/66),其表达强弱与肿瘤分级,大小,分期等无显着相关性.MVD值为12~96.3,与肿瘤分级(P等于0.005P等于0.000P等于0.011肿瘤体积较大时MVD50的病例(26.7%)少于50的病例(73.3%).ClinicopathologicalsignificanceofVEGFexpressionandmicrovasculardensityinrenalclearcellcarcinomaLuHaizhen,FengXiaoli,SunYuntian,YingJianming,ChenYan,ShiSusheng,LiuXiuyun.DepartmentofPathology,CancerHospital,ChineseAcademyofMedicalScience,Beijing100021,China

[Abstract]ObjectiveToevaluatevascularendothelialgrowthfactor(VEGF)expressionandmicrovasculardensity(MVD),andtheirclinicopathologicalsignificanceinclearcellrenalcarcinoma(CCRCC).MethodsImmunohistochemistrymethodwasusedtoexaminetheexpressionofVEGF.CD34stainingendothelialcellswereappliedtomeasuretheMVD.ResultsSixty-sixcasesofCCRCCwerecollected.VEGFexpressionsin36(54.5%)caseswerepositive.NosignificantrelationshipwasdetectedbetweenVEGFexpressionandclinicopathologicalparameters.ThelevelsofMVDweresignificantlylowerinadvancedTNMstaging(P等于0.000,highgrading(P等于0.005andmetastasizedtumors(P等于0.011.Inlargertumors,thecasesofMVD>,50(26.7%)(73.3%)TherewasnosignificantrelationshipbetweentheexpressionofVEGFandMVD,andneitherofthemwascorrelatedwiththerenalcapsuleinfiltration.ConclusionTheoverexpressionofVEGFinCCRCCshowthatitmaybethetargetmolecularfortreatment.ThedegreeofMVDisinverselycorrelatedwiththegradingandstagingofCCRCC,indicatingit'ssignificanceintheprognosisassesentofCCRCC.

文模板,文格式样本参考属性评定
有关论文范文主题研究: 关于内皮的论文范例 大学生适用: 专科论文、自考论文
相关参考文献下载数量: 73 写作解决问题: 毕业论文怎么写
毕业论文开题报告: 论文任务书、论文摘要 职称论文适用: 期刊目录、高级职称
所属大学生专业类别: 毕业论文怎么写 论文题目推荐度: 经典题目

[Keywords]Kidneyneoplas,Vascularendothelialgrowthfactors,Immunohistochemistry,Microvasculardensity

肾细胞癌(renalcellcarcinomaRCC)约占成人肾脏恶性肿瘤的90%,发病率仅次于膀胱癌,在泌尿系统恶性肿瘤中占第位血管丰富为其特点.

DOI:10.3760/cma.j.issn.1673-422X.2016.04.(001

作者单位:100021北京,中国医学科学院肿瘤医院病理科(鲁海珍,冯晓莉,孙耘田,应建明,石素胜,刘秀云),诊断科(陈雁)

Tel:010-8778750713552141545,办公室010-87787514