国际肿瘤学杂志
國際腫瘤學雜誌
국제종류학잡지
JOURNAL OF INTERNATIONAL ONCOLOGY
2012年
3期
237-240
,共4页
张宇%倪泽称%胡岚亭%张宁%汪清
張宇%倪澤稱%鬍嵐亭%張寧%汪清
장우%예택칭%호람정%장저%왕청
荧光原位杂交技术%尿路上皮肿瘤%染色体畸变%诊断
熒光原位雜交技術%尿路上皮腫瘤%染色體畸變%診斷
형광원위잡교기술%뇨로상피종류%염색체기변%진단
Fluorescence in situ hybridization%Urothelial cancinoma%Chromosome aberration%Diagnosis
目的 探讨双色荧光原位杂交技术( FISH)诊断膀胱尿路上皮肿瘤的临床应用价值.方法 标记为3、7、17号染色体着丝粒及9号染色体p16位点9p21区带探针,采用FISH对80例膀胱尿路上皮肿瘤患者尿液间期细胞核进行FISH,同时选取20例健康体检者作为正常对照组,建立阈值,以组织病理结果作为诊断“金标准”,统计染色体畸变情况,分析其与病理分期、分级的关系以及染色体畸变组合诊断膀胱尿路上皮肿瘤的敏感性.结果 3、7、17号染色体和9p21的畸变率分别为47.5%(38/80)、60.7%(49/80)、51.3%(41/80)和58.8%(47/80),3、7、9和17号染色体联合检测膀胱癌的阳性率为76.3%(61/80),畸变和肿瘤分期无相关性,3、7、17号染色体与肿瘤病理分级有显著相关性(P<0.05).结论 膀胱尿路上皮肿瘤的进展可能与染色体的畸变有关,FISH可以作为膀胱尿路上皮肿瘤诊断的一项重要方法,并可能在术后监测复发以及预后判断中具有重要临床意义.
目的 探討雙色熒光原位雜交技術( FISH)診斷膀胱尿路上皮腫瘤的臨床應用價值.方法 標記為3、7、17號染色體著絲粒及9號染色體p16位點9p21區帶探針,採用FISH對80例膀胱尿路上皮腫瘤患者尿液間期細胞覈進行FISH,同時選取20例健康體檢者作為正常對照組,建立閾值,以組織病理結果作為診斷“金標準”,統計染色體畸變情況,分析其與病理分期、分級的關繫以及染色體畸變組閤診斷膀胱尿路上皮腫瘤的敏感性.結果 3、7、17號染色體和9p21的畸變率分彆為47.5%(38/80)、60.7%(49/80)、51.3%(41/80)和58.8%(47/80),3、7、9和17號染色體聯閤檢測膀胱癌的暘性率為76.3%(61/80),畸變和腫瘤分期無相關性,3、7、17號染色體與腫瘤病理分級有顯著相關性(P<0.05).結論 膀胱尿路上皮腫瘤的進展可能與染色體的畸變有關,FISH可以作為膀胱尿路上皮腫瘤診斷的一項重要方法,併可能在術後鑑測複髮以及預後判斷中具有重要臨床意義.
목적 탐토쌍색형광원위잡교기술( FISH)진단방광뇨로상피종류적림상응용개치.방법 표기위3、7、17호염색체착사립급9호염색체p16위점9p21구대탐침,채용FISH대80례방광뇨로상피종류환자뇨액간기세포핵진행FISH,동시선취20례건강체검자작위정상대조조,건립역치,이조직병리결과작위진단“금표준”,통계염색체기변정황,분석기여병리분기、분급적관계이급염색체기변조합진단방광뇨로상피종류적민감성.결과 3、7、17호염색체화9p21적기변솔분별위47.5%(38/80)、60.7%(49/80)、51.3%(41/80)화58.8%(47/80),3、7、9화17호염색체연합검측방광암적양성솔위76.3%(61/80),기변화종류분기무상관성,3、7、17호염색체여종류병리분급유현저상관성(P<0.05).결론 방광뇨로상피종류적진전가능여염색체적기변유관,FISH가이작위방광뇨로상피종류진단적일항중요방법,병가능재술후감측복발이급예후판단중구유중요림상의의.
Objective To evaluate the clinical application value of dual color fluorescence in-situ hybridization (FISH) in detecting urothelial carcinoma of the urinary bladder.Methods The probes of chromosome 3,7,17centromeres and chromosome 9p21 region (p16) were labeled by random primer method.FISH was performed on interphase nuclei of 80 urine specimens of cancer of the urinary bladder and 20 cases of healthy persons served as normal controls.Threshold value was established.The pathological diagnosis was the "golden standard".Chromosome aberration was counted.The correlations between chromosome aberration and pathologic grading and staging and their sensibility of diagnosis for urothelial carcinoma of the urinary bladder were analyzed. Results The rate of numerical aberration of chromosome 3,7,17,9p21 was 47.5%(38/80),60.7% (49/80),51.3% (41/80) and 58.8% (47/80) respectively.The positive rate of the combined use of 3,7,17 and 9p21 chromosome probes for detecting urothelial carcinoma of urinary bladder was 76.3% (61/80).The aberrations had no correlation to tumor stage.The aberration of chromosome 3,7 and 17 were correlated to pathologic grade significantly (P < 0.05).Conclusion The progression of urothelial carcinoma of the urinary bladder is related to the aberrations of chromosome.FISH is believed to be a very important method in diagnosis of urothelial carcinoma of the urinary bladder,which may have important clinical significance for the postoperative recurrence detection and prognosis.