期刊文献+

胃癌组织中微小RNA-1468的表达及临床意义 被引量:2

Expression and clinical significance of microRNA-1468 in gastric cancer tissues
下载PDF
导出
摘要 目的探讨微小RNA-1468(miR-1468)在胃癌组织中的表达并分析其临床意义。方法收集2013年6月至2015年1月于本院手术切除的胃癌组织123例和对应癌旁组织78例,采用实时定量PCR(QPCR)法检测以上组织中的miR-1468水平并比较其在癌组织和癌旁组织中的表达差异,采用受试者工作特征曲线(ROC)分析组织miR-1468水平诊断胃癌的效能,分析癌组织miR-1468水平与胃癌临床病理特征(性别、年龄、肿瘤大小、Lauren分型、浸润深度、淋巴结转移、组织分化和TNM分期)的关系,采用Kaplan-Meier法进行生存分析并比较胃癌患者中不同miR-1468水平的预后情况。结果胃癌组织的miR-1468水平为2.524±1.282,高于癌旁组织的1.122±0.850(P<0.05);ROC分析显示组织miR-1468水平诊断胃癌的曲线下面积为0.844(95%CI:0.787~0.900),当以约登指数最大的1.199为诊断界值时,其灵敏度和特异度分别为87.0%和74.4%。胃癌组织miR-1468水平与性别、年龄、Lauren分型和组织分化无关(P>0.05),而与肿瘤大小、浸润深度、淋巴结转移和TNM分期有关(P<0.05);51例Ⅲ期胃癌患者中,miR-1468低表达者的中位无病生存期为40.0个月,优于高表达者的29.0个月(P<0.05),而miR-1468低表达者的中位生存期为56.0个月,与高表达组45.0个月的差异无统计学意义(P>0.05)。结论胃癌组织中miR-1468高表达且与肿瘤大小、浸润深度、淋巴结转移和TNM分期有关,高表者的预后较差,在胃癌的诊治和预后预测中有一定价值。 Objective To investigate the expression of microRNA-1468(miR-1468) in gastric cancer and analyze its clinical significance. Methods One hundred and twenty-three gastric cancer tissues and 78 corresponding paracancerous tissues were collected from our hospital from June 2013 to January 2015. The levels of miR-1468 in the above tissues were detected by real-time quantitative PCR(QPCR) and their distribution differences in cancer tissues and paracancerous tissues were compared. The diagnostic efficacy of miR-1468 in gastric cancer tissues was analyzed by receiver operating characteristic curve(ROC). The relationship between miR-1468 level and clinicopathological characteristics of gastric cancer(gender, age, size of tumors, Lauren classification, depth of invasion, lymph node metastasis, tissue differentiation and TNM stage) was analyzed. Kaplan-Meier survival analysis was used to compare the prognosis of different levels of miR-1468 expression in gastric cancer patients. Results The level of miR-1468 in gastric cancer tissues was 2.524±1.282, higher than 1.122±0.850 in adjacent tissues(P<0.05). ROC analysis showed that the area under the curve of miR-1468 in gastric cancer tissues was 0.844(95% CI: 0.787-0.900), and when 1.199 with the largest Yoden index as the diagnostic threshold, the sensitivity and specificity were 87.0% and 74.4%. In 51 gastric cancer patients with stage Ⅲ, the median disease-free survival in the low expression group was 40.0 months, higher than 29.0 months in the high expression group(P<0.05). The median overall survival in the low expression group was 56.0 months, similar to 45.0 months in the high expression group(P>0.05). Conclusion The high expression of miR-1468 in gastric cancer is related to tumor size, depth of invasion, lymph node metastasis and TNM stage. The prognosis of high expression is poor, and it has a certain value in the diagnosis, treatment and prognosis prediction of gastric cancer.
作者 郭东栋 李晓艳 张福林 GUO Dongdong;LI Xiaoyan;ZHANG Fulin(Department of Oncology,Yan'an People's Hospital,Yan'an 716000,China)
出处 《临床肿瘤学杂志》 CAS 北大核心 2019年第5期396-400,共5页 Chinese Clinical Oncology
关键词 胃癌 微小RNA-1468 临床意义 预后 Gastric cancer MicroRNA-1468 Clinical significance Prognosis
  • 相关文献

参考文献3

二级参考文献26

  • 1Tindara Franchina,Valeria Amodeo,Giuseppe Bronte,Giuseppina Savio,Giuseppina R.R. Ricciardi,Maria Picciotto,Antonio Russo,Antonio Giordano,Vincenzo Adamo.Circulating miR‐22, miR‐24 and miR‐34a as Novel Predictive Biomarkers to Pemetrexed‐Based Chemotherapy in Advanced Non‐Small Cell Lung Cancer[J]. J. Cell. Physiol. . 2014 (1) 被引量:1
  • 2Dhiraj Yadav,Albert B. Lowenfels.The Epidemiology of Pancreatitis and Pancreatic Cancer[J]. Gastroenterology . 2013 (6) 被引量:1
  • 3K. E. Poruk,D. Z. Gay,K. Brown,J. D. Mulvihill,K. M. Boucher,C. L. Scaife,M. A. Firpo,S. J. Mulvihill.The Clinical Utility of CA 19-9 in Pancreatic Adenocarcinoma: Diagnostic and Prognostic Updates[J]. Current Molecular Medicine . 2013 (3) 被引量:1
  • 4Bo Ling,Gui-Xue Wang,Guang Long,Ju-Hui Qiu,Zhong-Lei Hu.Tumor suppressor miR -22 suppresses lung cancer cell progression through post-transcriptional regulation of ErbB3[J]. Journal of Cancer Research and Clinical Oncology . 2012 (8) 被引量:1
  • 5N. Lubezky,S. Lowenstein,M. Ben-Haim,E. Brazowski,S. Marmor,M. Pasmanik-Chor,Varda Oron-Karni,G. Rechavi,J.M. Klausner,G. Lahat.MicroRNA Expression Signatures in Intraductal Papillary Mucinous Neoplasm of the Pancreas[J]. Surgery . 2012 被引量:1
  • 6Jun Shen,Sanford A. Stass,Feng Jiang.MicroRNAs as potential biomarkers in human solid tumors[J]. Cancer Letters . 2012 被引量:2
  • 7Xianwei Wang,Jianfeng Zhao,Jianhua Huang,Huihuan Tang,Shuyi Yu,Yuxiang Chen.The regulatory roles of miRNA and methylation on oncogene and tumor suppressor gene expression in pancreatic cancer cells[J]. Biochemical and Biophysical Research Communications . 2012 (1) 被引量:1
  • 8Wei Yan,Wei Zhang,Lihua Sun,Yanwei Liu,Gan You,Yongzhi Wang,Chunsheng Kang,Yongping You,Tao Jiang.Identification of MMP-9 specific microRNA expression profile as potential targets of anti-invasion therapy in glioblastoma multiforme[J]. Brain Research . 2011 被引量:1
  • 9Yi Ting,Daniel J. Medina,Roger K. Strair,Dale G. Schaar.Differentiation-associated miR-22 represses Max expression and inhibits cell cycle progression[J]. Biochemical and Biophysical Research Communications . 2010 (3) 被引量:1
  • 10ThomasGreither,Lukasz F.Grochola,AndrejUdelnow,ChristineLautenschl?ger,PeterWürl,HelgeTaubert.Elevated expression of microRNAs 155, 203, 210 and 222 in pancreatic tumors is associated with poorer survival[J]. Int. J. Cancer . 2009 (1) 被引量:1

共引文献17

同被引文献19

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部