刘莎莎①②, 岳冬丽①, 陈新峰①, 平玉①②, 张毅①②. 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. DOI: 10.3969/j.issn.1000-8179.2016.18.656
引用本文: 刘莎莎①②, 岳冬丽①, 陈新峰①, 平玉①②, 张毅①②. 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. DOI: 10.3969/j.issn.1000-8179.2016.18.656
Shasha LIU1, 2, Dongli YUE1, Xinfeng CHEN1, Yu PING1. Clinical significance of microrna- 625 expression in esophageal squamous cell carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2016, 43(18): 825-829. DOI: 10.3969/j.issn.1000-8179.2016.18.656
Citation: Shasha LIU1, 2, Dongli YUE1, Xinfeng CHEN1, Yu PING1. Clinical significance of microrna- 625 expression in esophageal squamous cell carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2016, 43(18): 825-829. DOI: 10.3969/j.issn.1000-8179.2016.18.656

MicroRNA-625 在食管鳞癌中的表达及临床意义*

Clinical significance of microrna- 625 expression in esophageal squamous cell carcinoma

  • 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。

     

    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 in86paired 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.

     

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