中华胃肠外科杂志
中華胃腸外科雜誌
중화위장외과잡지
CHINESE JOURNAL OF GASTROINTESTINAL SURGERY
2009年
6期
623-626
,共4页
张益%周总光%王玲%张鹏%王默进%崔长富%关键婷%陈柯玲%詹兰
張益%週總光%王玲%張鵬%王默進%崔長富%關鍵婷%陳柯玲%詹蘭
장익%주총광%왕령%장붕%왕묵진%최장부%관건정%진가령%첨란
结直肠肿瘤%实时荧光定量聚合酶链反应%微RNAs
結直腸腫瘤%實時熒光定量聚閤酶鏈反應%微RNAs
결직장종류%실시형광정량취합매련반응%미RNAs
Colorectal neoplasms%Quantitative real-time PCR%MicroRNAs
目的 探讨miR-21和miR-125在结直肠癌中的表达与临床病理特征之间的关系.方法 选取2006年7月至2007年12月经手术切除的原发性结直肠癌标本100例,采用实时荧光定量PCR分析miR-21和miR-125的表达情况.结果 相对于癌旁组织,100例结直肠癌组织中miR-21表达上调2.3倍(P=0.025),其表达与TNM分期(P=0.028)以及浸润深度有关(P=0.023);而miR-125在癌组织中的表达则下调3.3倍(P=0.005),其表达与TNM分期、浸润深度和远处转移无明显关联(P>0.05).结论 miR-21可能参与了结直肠癌的发生和发展;而miR-125可能未参与.
目的 探討miR-21和miR-125在結直腸癌中的錶達與臨床病理特徵之間的關繫.方法 選取2006年7月至2007年12月經手術切除的原髮性結直腸癌標本100例,採用實時熒光定量PCR分析miR-21和miR-125的錶達情況.結果 相對于癌徬組織,100例結直腸癌組織中miR-21錶達上調2.3倍(P=0.025),其錶達與TNM分期(P=0.028)以及浸潤深度有關(P=0.023);而miR-125在癌組織中的錶達則下調3.3倍(P=0.005),其錶達與TNM分期、浸潤深度和遠處轉移無明顯關聯(P>0.05).結論 miR-21可能參與瞭結直腸癌的髮生和髮展;而miR-125可能未參與.
목적 탐토miR-21화miR-125재결직장암중적표체여림상병리특정지간적관계.방법 선취2006년7월지2007년12월경수술절제적원발성결직장암표본100례,채용실시형광정량PCR분석miR-21화miR-125적표체정황.결과 상대우암방조직,100례결직장암조직중miR-21표체상조2.3배(P=0.025),기표체여TNM분기(P=0.028)이급침윤심도유관(P=0.023);이miR-125재암조직중적표체칙하조3.3배(P=0.005),기표체여TNM분기、침윤심도화원처전이무명현관련(P>0.05).결론 miR-21가능삼여료결직장암적발생화발전;이miR-125가능미삼여.
Objective To investigate the expression of microRNA(miR)-21 and miR-125 in colorectal cancer (CRC) and its relationship with clinicopathological features. Methods Quantitative real-time PCR was applied to examine the expression of miR-21 and miR-125 in 100 primary CRC specimens which were diagnosed and operated in West China Hospital between 2006 and 2007, in comparison with the corresponding normal mucosa specimens. The relationship between the expression of miRNAs and clinicopathological features was analyzed. Results The expression of miR-21 in CRC was up-regulated by 2.3 times compared to normal mucosa (P=0.025), while the expression of miR-125 was down-regulated by 3.3 times in comparison with normal mucosa(P=0.005). Furthermore, the expression of miR-21 was related to TNM stage (P=0.028) and local invasion (P=0.023). On the other hand, no significant relationship was found between the expression of miR-125 and clinicopathological features (P>0.05). Conclusion The over-expression of miR-21 may play a role in the development and progression of CRC, while miR-125 may not be related to the pathogenesis of CRC.