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Meta-analysis of human lung cancer microRNA expression profiling studies comparing cancer tissues with normal tissues

机译:对人肺癌组织与正常组织进行比较的人类肺癌microRNA表达谱研究的荟萃分析

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Background Lung cancer is the major cause of cancer death globally, it is often diagnosed at an advanced stage and has one of the lowest survival rates of any type of cancer. The common interest in the field of lung cancer research is the identification of biomarkers for early diagnosis and accurate prognosis. There is increasing evidence to suggest that microRNAs play important and complex roles in lung cancer. Methods A meta-analysis was conducted to review the published microRNA expression profiling studies that compared the microRNAs expression profiles in lung cancer tissues with those in normal lung tissues. A vote-counting strategy that considers the total number of studies reporting its differential expression, the total number of tissue samples used in the studies and the average fold change was employed. Results A total of 184 differentially expressed microRNAs were reported in the fourteen microRNA expression profiling studies that compared lung cancer tissues with normal tissues, with 61 microRNAs were reported in at least two studies. In the panel of consistently reported up-regulated microRNAs, miR-210 was reported in nine studies and miR-21 was reported in seven studies. In the consistently reported down-regulated microRNAs, miR-126 was reported in ten studies and miR-30a was reported in eight studies. Four up-regulated microRNAs (miR-210, miR-21, miR-31 and miR-182) and two down-regulated mcroiRNAs (miR-126 and miR-145) were consistently reported both in squamous carcinoma and adenocarcinoma-based subgroup analysis, with the other 14 microRNAs solely reported in one or the other subset. Conclusions In conclusion, the top two most consistently reported up-regulated microRNAs were miR-210 and miR-21. The results of this meta-analysis of human lung cancer microRNA expression profiling studies might provide some clues of the potential biomarkers in lung cancer. Further mechanistic and external validation studies are needed for their clinical significance and role in the development of lung cancer.
机译:背景技术肺癌是全球癌症死亡的主要原因,它经常被诊断为晚期,并且是任何类型癌症中最低的生存率之一。肺癌研究领域的共同兴趣是为早期诊断和准确预后确定生物标志物。越来越多的证据表明,microRNA在肺癌中起着重要而复杂的作用。方法进行荟萃分析,回顾已发表的microRNA表达谱研究,该研究比较了肺癌组织和正常肺组织中的microRNA表达谱。采用一种计票策略,该策略考虑了报告其差异表达的研究总数,研究中使用的组织样本总数以及平均倍数变化。结果十四项microRNA表达谱研究共报告了184个差异表达的microRNA,将肺癌组织与正常组织进行了比较,至少两项研究报告了61种microRNA。在持续报道的上调的microRNA中,有9项研究报道了miR-210,而7项研究报道了miR-21。在一致报道的下调的microRNA中,十项研究报道了miR-126,八项研究报道了miR-30a。在鳞癌和基于腺癌的亚组分析中一致报告了四个上调的microRNA(miR-210,miR-21,miR-31和miR-182)和两个下调的mcroiRNA(miR-126和miR-145)。 ,另外14个microRNA仅在一个或另一个子集中报告。结论总之,最一致报告的前两个最上调的microRNA是miR-210和miR-21。人类肺癌microRNA表达谱研究的荟萃分析结果可能为肺癌的潜在生物标志物提供一些线索。由于它们的临床意义和在肺癌发展中的作用,需要进一步的机理和外部验证研究。

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