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MicroRNA-625 在食管鳞癌中的表达及临床意义*
引用本文:刘莎莎,岳冬丽,陈新峰,平玉,张毅.MicroRNA-625 在食管鳞癌中的表达及临床意义*[J].中国肿瘤临床,2016,43(18):825-829.
作者姓名:刘莎莎  岳冬丽  陈新峰  平玉  张毅
作者单位:作者单位:①郑州大学第一附属医院生物治疗中心(郑州市450052);②郑州大学生命科学学院
基金项目:本文课题受卫生部科技攻关项目(编号201501004)资助@@@@This work was supported by the Foundation for Science and Technology Program of Ministry of Public Health
摘    要:目的:探讨microRNA- 625(miR-625)在食管鳞癌(esophageal squamous cell carcinoma ,ESCC)中的表达及其与临床参数的相关性,探究miR-625 对ESCC细胞系KYSE70迁移和增殖的影响。方法:实时荧光定量(real-time polymerase chain reaction ,PCR )检测2014年2 月至2015年4 月郑州大学第一附属医院手术切除的86例ESCC及癌旁正常组织、ESCC细胞系和正常永生化食管上皮细胞系中miR-625 的表达,统计学分析其表达水平与ESCC患者临床病理参数及预后的相关性。Transwell 实验检测miR-625 对细胞迁移能力的影响,细胞计数Kit- 8(CCK-8)法检测miR-625 对细胞增殖的影响。结果:ESCC组织中miR-625 的表达明显低于癌旁正常组织(P < 0.05),ESCC细胞系中miR-625 表达水平与正常永生化食管上皮细胞相比,显著下调(P < 0.05)。miR-625 的表达与肿瘤直径、分化程度及淋巴结转移呈负相关(P < 0.05)。 随访数据提示miR-625 低表达组患者预后更差(P <0.05)。 miR-625 能够抑制ESCC的迁移和增殖(P < 0.05)。 结论:miR-625 作为抑癌基因参与ESCC的发生发展,提示miR-625 可能作为一个ESCC治疗靶点和预后判断的分子标志物。 

关 键 词:miR-625    食管鳞癌?    迁移?    增殖    预后
收稿时间:2016-06-06

Clinical significance of microrna-625 expression in esophageal squamous cell carcino-ma
Institution:1Biotherapy Center, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China;
Abstract:Objective: To analyze the correlation of miR-625 expression with clinicopathological characteristics in esophageal squa-mous cell carcinoma (ESCC) and to explore the effect of miR-625 on the migration and proliferation of ESCC cells. Methods:The expres-sion level of miR-625 was determined through real-time PCR in 86 paired human ESCC tissue specimens and tumor-adjacent normal esophageal tissue specimens, ESCC cell lines, and esophageal epithelial cell line. The associations of miR-625 expression with clinico-pathological characteristics and survival in ESCC patients were analyzed. Transwell and CCK-8 assays were performed to examine the effect of miR-625 expression on migration and proliferation of ESCC cells. Results:Compared with tumor-adjacent normal specimens, miR-625 was significantly downregulated in ESCC tissue specimens (P<0.05). MiR-625 expression was decreased in ESCC cell lines com-pared with human esophageal epithelial cell lines (P<0.05). Lower miR-625 expression was associated with poorer prognosis and sur-vival. The migration and proliferation abilities of ESCC cells were inhibited by miR-625 overexpression (P<0.05). Conclusion:MiR-625 acts as a tumor suppressor gene in the development and progression of ESCC, suggesting that miR-625 may serve as an efficient prog-nosis biomarker and a potential therapeutic target for ESCC.
Keywords:miR-625  ESCC  migration  proliferation  prognosis
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