中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2015年
4期
695-697
,共3页
徐学虎%吴小兵%伍尚标%孙嫣%刘海波%陈戎
徐學虎%吳小兵%伍尚標%孫嫣%劉海波%陳戎
서학호%오소병%오상표%손언%류해파%진융
微小RNA-193b%结肠癌%直肠癌%诊断标记
微小RNA-193b%結腸癌%直腸癌%診斷標記
미소RNA-193b%결장암%직장암%진단표기
MicroRNA-193b%Colon cancer%Rectal cancer%Diagnostic marker
目的 观察微小RNA(miRNA,miR)-193b在结直肠癌(CRC)中的表达水平,探讨其作为CRC诊断标记的潜能.方法 采用实时荧光定量聚合酶链反应(FQ-PCR)分析miR-193b在Ⅱ、Ⅲ、Ⅳ期及整体CRC中的表达水平,采用t检验及受试者特征曲线(ROC)分析miR-193b作为CRC诊断标记的敏感性和特异性.并应用Cluster聚类法分析其表达水平与CRC分期的相关性.结果 miR-193b在Ⅱ、Ⅲ、Ⅳ期及整体CRC中分别下调3.860倍(P<0.05)、2.680倍(P<0.05)、5.280倍(P<0.05)、3.410倍(P<0.05).miR-193b筛查CRC的特异性和敏感性分别是61.29%和77.42%,曲线下面积(AUC)为0.728.而其表达水平和CRC的分期无明显相关.结论 miR-193b具有作为CRC诊断标记的潜能.
目的 觀察微小RNA(miRNA,miR)-193b在結直腸癌(CRC)中的錶達水平,探討其作為CRC診斷標記的潛能.方法 採用實時熒光定量聚閤酶鏈反應(FQ-PCR)分析miR-193b在Ⅱ、Ⅲ、Ⅳ期及整體CRC中的錶達水平,採用t檢驗及受試者特徵麯線(ROC)分析miR-193b作為CRC診斷標記的敏感性和特異性.併應用Cluster聚類法分析其錶達水平與CRC分期的相關性.結果 miR-193b在Ⅱ、Ⅲ、Ⅳ期及整體CRC中分彆下調3.860倍(P<0.05)、2.680倍(P<0.05)、5.280倍(P<0.05)、3.410倍(P<0.05).miR-193b篩查CRC的特異性和敏感性分彆是61.29%和77.42%,麯線下麵積(AUC)為0.728.而其錶達水平和CRC的分期無明顯相關.結論 miR-193b具有作為CRC診斷標記的潛能.
목적 관찰미소RNA(miRNA,miR)-193b재결직장암(CRC)중적표체수평,탐토기작위CRC진단표기적잠능.방법 채용실시형광정량취합매련반응(FQ-PCR)분석miR-193b재Ⅱ、Ⅲ、Ⅳ기급정체CRC중적표체수평,채용t검험급수시자특정곡선(ROC)분석miR-193b작위CRC진단표기적민감성화특이성.병응용Cluster취류법분석기표체수평여CRC분기적상관성.결과 miR-193b재Ⅱ、Ⅲ、Ⅳ기급정체CRC중분별하조3.860배(P<0.05)、2.680배(P<0.05)、5.280배(P<0.05)、3.410배(P<0.05).miR-193b사사CRC적특이성화민감성분별시61.29%화77.42%,곡선하면적(AUC)위0.728.이기표체수평화CRC적분기무명현상관.결론 miR-193b구유작위CRC진단표기적잠능.
Objective To analysis the expression level of microRNA (miRNA,miR)-193b in colorectal cancer (CRC),and give a research on the sensitivity and specificity of distinguishing CRC from normal people.Methods Real time-Polymerase Chain Reaction was used to analysis the expression level of miR-193b between tumor and paired normal tissues in Ⅱ,Ⅲ,Ⅳ stages of CRC,t-test and Receiver operating characteristic (ROC) curve was performed to identify evaluate the specificity and sensitivity of using miR-193b as biomarker to discriminate CRC patients from normal person with P <0.05.Cluster was performed to find the relationship between the expressing level and cancer staging.Results miR-193b was performed down-regulated 3.860 folds (P < 0.05),2.680 folds (P < 0.05),5.280 folds (P < 0.05)and 3.410 folds (P <0.05) in stage Ⅱ,Ⅲ,Ⅳ and mixtured cancer sample.MiR-193b could screening CRC from normal group with high sensitivity and specificity,but the dysregulation of miR-193b has no relation with pathological stage.Conclusion miR-193b showed high likely to be potential diagnostic marker of CRC.