中国癌症杂志 ›› 2013, Vol. 23 ›› Issue (7): 487-492.doi: 10.3969/j.issn.1007-3969.2013.07.002

• 论著 • 上一篇    下一篇

MicroRNA-31在食管鳞状细胞癌中的表达及其与预后的关系

罗君,凌志强,彭兵锋,袁嘉敏,郑智国,毛伟敏   

  1. 浙江省肿瘤医院,浙江省肿瘤研究所,浙江省胸部肿瘤( 肺、食管) 诊治技术研究重点实验室,浙江 杭州310022
  • 出版日期:2013-07-25 发布日期:2014-03-03
  • 通信作者: 凌志强 E-mail:lingzq@hotmail.com
  • 基金资助:
    卫生部科研基金(No:WKJ2010-2-004);浙江省自然基金项目(No:Y2091110)

The expression of microRNA-31 in esophageal squamous cell carcinoma and its prognostic value

LUO Jun,LING Zhi-qiang,PENG Bing-feng,YUAN Jia-min,ZHENG Zhi-guo,MAO Wei-min   

  1. Zhejiang Province Cancer Hospital, Zhejiang Cancer Research Institure, Zhejiang Key Laboratory of the Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou Zhejiang 310022, China
  • Published:2013-07-25 Online:2014-03-03
  • Contact: LING Zhi-qiang E-mail: lingzq@hotmail.com

摘要:

背景与目的:研究发现,许多微小RNA(microRNAsmiRNAs)与恶性肿瘤密切相关,其中miR-31(microRNA-31)在许多肿瘤中呈异常改变。中国是食管鳞状上皮细胞癌(esophageal squamous cell carcinomaESCC)最高发的地区之一。本研究旨在调查miR-31ESCC中的表达水平与临床病理学因素以及预后的关系。方法:采用实时反转录聚合酶链反应(reverse transcription-polymerase chain reactionRTPCR)技术检测食管癌细胞株KYSE410EC1EC9706,以及81ESCC组织和癌旁正常组织中miR-31的表达水平。结果与临床资料和随访结果结合作统计分析。结果:3ESCC细胞株以及75.31%ESCC组织中,miR-31表达上调。并且miR-31的高表达与更严重的淋巴结转移(P=0.043)、更深的浸润深度(P=0.002)以及更晚期的病理分期有关(P=0.027),而与其他临床病理学因素无关(P>0.05)。此外,miR-31的高表达与较差的无进展生存期(progression-free survivalPFS)有关(Kaplan-Meier分析P=0.014,多变量Cox分析P=0.021)结论:miR-31可能是ESCC一项新的诊断和预后评价指标。

关键词: 食管鳞状细胞癌, miR-31, 临床病理学, 生存期

Abstract:

Background and purpose: It was reported that many microRNAs (miRNAs) have close relation with carcinomas. miR-31 (microRNA-31) shows abnormal change in numerous cancers. China is one of the most high-risk areas of esophageal squamous cell carcinoma (ESCC). The aim of the present study was to investigate the expression of miR-31 in ESCC, and analyze the relationship of its expression with clinicopathological features and prognosis. Methods: The expression of miR-31 in KYSE410, EC1 and EC9706 cell lines, as well as 81 cases of ESCC tissues and adjacent normal esophageal tissues were detected by real-time reverse transcription-polymerase chain reaction (RT-PCR). The result was combined with clinical and follow-up data and statistical analysis was conducted. Results: MiR-31 was up-expression in 3 cell lines and 75.31% of the ESCC tissues. miR-31 up-expression was positively related to severer lymph node metastasis (P=0.043), deeper invasion of tumors (P=0.002) and advanced pathological stage (P=0.027). There was no relationship of miR-31 with other clinicopathological features (P>0.05). Furthermore, high expression of miR-31 was associated with poor progression-free survival (PFS) in 81 ESCC patients by Kaplan-Meier analysis (P=0.014) and by multivariate Cox analysis (P=0.021). Conclusion: Our results identified miR-31 may be a new diagnostic criteria and prognostic biomarker for ESCC.

Key words: Esophageal squamous cell carcinoma, miR-31, Clinicopathology, Survival