检验医学与临床
檢驗醫學與臨床
검험의학여림상
JOURNAL OF LABORATORY MEDICINE AND CLINICAL SCIENCES
2015年
3期
314-316
,共3页
林剑勇%邓益斌%罗艳红%陆小婵%黄永秩
林劍勇%鄧益斌%囉豔紅%陸小嬋%黃永秩
림검용%산익빈%라염홍%륙소선%황영질
miRNA-449a%肺癌%miRNAs%分子诊断
miRNA-449a%肺癌%miRNAs%分子診斷
miRNA-449a%폐암%miRNAs%분자진단
miRNA-449a%lung cancer%microRNAs%molecular diagnostic
目的:探讨miRNA‐449a在肺癌细胞中的表达及其临床应用价值。方法收集右江民族医学院附属医院2011年1月1日至2013年6月30日收治的58例肺癌患者作为研究对象,采用逆转录荧光定量聚合酶链反应检测miRNA‐449a在肺癌组织和癌旁正常组织中的表达量,分析miRNA‐449a与临床病理特征的关系,并采用荧光电子显微镜观察miRNA‐449a模拟物对体外培养肺癌细胞株95D细胞凋亡的影响。结果鳞癌组和腺癌组miR‐NA‐449a平均表达量均明显低于癌旁正常对照组(t=6.712,P<0.05;t=4.572,P<0.05),其相对表达量与瘤体大小(U=78.412,P=0.012)有关,与患者年龄(U=920.000,P=0.615)、性别(U=800.000,P=0.215)、病理类型(χ2=4.221,P=0.155)和临床分期(U=754.000,P=0.009)无关。与阴性对照组比较,miRNA‐449a模拟物可明显促进肺癌细胞的凋亡,且呈剂量依赖性。结论 miRNA‐449a在肺癌组织中呈低表达,可诱导肺癌细胞凋亡,发挥抑癌基因的作用,可能成为肺癌早期诊断与治疗的新分子靶标。
目的:探討miRNA‐449a在肺癌細胞中的錶達及其臨床應用價值。方法收集右江民族醫學院附屬醫院2011年1月1日至2013年6月30日收治的58例肺癌患者作為研究對象,採用逆轉錄熒光定量聚閤酶鏈反應檢測miRNA‐449a在肺癌組織和癌徬正常組織中的錶達量,分析miRNA‐449a與臨床病理特徵的關繫,併採用熒光電子顯微鏡觀察miRNA‐449a模擬物對體外培養肺癌細胞株95D細胞凋亡的影響。結果鱗癌組和腺癌組miR‐NA‐449a平均錶達量均明顯低于癌徬正常對照組(t=6.712,P<0.05;t=4.572,P<0.05),其相對錶達量與瘤體大小(U=78.412,P=0.012)有關,與患者年齡(U=920.000,P=0.615)、性彆(U=800.000,P=0.215)、病理類型(χ2=4.221,P=0.155)和臨床分期(U=754.000,P=0.009)無關。與陰性對照組比較,miRNA‐449a模擬物可明顯促進肺癌細胞的凋亡,且呈劑量依賴性。結論 miRNA‐449a在肺癌組織中呈低錶達,可誘導肺癌細胞凋亡,髮揮抑癌基因的作用,可能成為肺癌早期診斷與治療的新分子靶標。
목적:탐토miRNA‐449a재폐암세포중적표체급기림상응용개치。방법수집우강민족의학원부속의원2011년1월1일지2013년6월30일수치적58례폐암환자작위연구대상,채용역전록형광정량취합매련반응검측miRNA‐449a재폐암조직화암방정상조직중적표체량,분석miRNA‐449a여림상병리특정적관계,병채용형광전자현미경관찰miRNA‐449a모의물대체외배양폐암세포주95D세포조망적영향。결과린암조화선암조miR‐NA‐449a평균표체량균명현저우암방정상대조조(t=6.712,P<0.05;t=4.572,P<0.05),기상대표체량여류체대소(U=78.412,P=0.012)유관,여환자년령(U=920.000,P=0.615)、성별(U=800.000,P=0.215)、병리류형(χ2=4.221,P=0.155)화림상분기(U=754.000,P=0.009)무관。여음성대조조비교,miRNA‐449a모의물가명현촉진폐암세포적조망,차정제량의뢰성。결론 miRNA‐449a재폐암조직중정저표체,가유도폐암세포조망,발휘억암기인적작용,가능성위폐암조기진단여치료적신분자파표。
Objective To investigate the expression and and its clinical significance of miRNA‐449a in lung cancer. Methods Totally 58 patients with lung cancer were selected as research objects from Affiliated Hospital of Youjiang Medical College for Nationalities on January 1, 2011 to June 30, 2013. The expression of miRNA‐449a in lung cancer tissues and matched normal tissues were detected by real time PCR. And the relationship between clinical pathological features and the level of miRNA‐449a were analysed. Fluorescent electronic microscope was applied to analyze the apoptosis after transfecting mimics of miRNA‐449a into non‐small cell lung cancer. Results The level of miRNA‐449a was significantly lower in squamous carcinoma group and adenocarcinoma group than that of control group(t=6. 712, P<0. 05 ;t=4. 572, P<0. 05 ;respectively). There was correlation between miRNA‐449a and tumor size(U=78. 412, P=0. 012) and no correlation between miRNA‐449a and age(U=920. 000, P=0. 615), gender(U=800. 000, P=0. 215), pathological type(χ2 =4. 221, P= 0. 155)and clinic stage(U=754. 000, P= 0. 009), all P>0. 05. Compared with negative control group, miRNA‐449a mimics could induce apoptosis of lung cancer cell 95D with dose‐effect dependent. Conclusion miRNA‐449a is lower expression in lung cancer, can induced apoptosis, which maybe play a role as a tumor suppressor gene, and as a new molecular targets of early diagnosis and treatment of lung cancer.