Joint Laboratory of Immunogenomics, Zhoushan Hospital-BIGCAS, Zhejiang, People's Republic of China.
PLoS One. 2011;6(10):e26502. doi: 10.1371/journal.pone.0026502. Epub 2011 Oct 27.
Using DNA microarrays, we generated both mRNA and miRNA expression data from 6 non-small cell lung cancer (NSCLC) tissues and their matching normal control from adjacent tissues to identify potential miRNA markers for diagnostics. We demonstrated that hsa-miR-96 is significantly and consistently up-regulated in all 6 NSCLCs. We validated this result in an independent set of 35 paired tumors and their adjacent normal tissues, as well as their sera that are collected before surgical resection or chemotherapy, and the results suggested that hsa-miR-96 may play an important role in NSCLC development and has great potential to be used as a noninvasive marker for diagnosing NSCLC. We predicted potential miRNA target mRNAs based on different methods (TargetScan and miRanda). Further classification of miRNA regulated genes based on their relationship with miRNAs revealed that hsa-miR-96 and certain other miRNAs tend to down-regulate their target mRNAs in NSCLC development, which have expression levels permissive to direct interaction between miRNAs and their target mRNAs. In addition, we identified a significant correlation of miRNA regulation with genes coincide with high density of CpG islands, which suggests that miRNA may represent a primary regulatory mechanism governing basic cellular functions and cell differentiations, and such mechanism may be complementary to DNA methylation in repressing or activating gene expression.
利用 DNA 微阵列,我们从 6 个非小细胞肺癌(NSCLC)组织及其相邻组织的正常对照中生成了 mRNA 和 miRNA 表达数据,以鉴定用于诊断的潜在 miRNA 标志物。我们证明 hsa-miR-96 在所有 6 个 NSCLC 中均显著且一致地上调。我们在独立的 35 对肿瘤及其相邻正常组织以及手术切除或化疗前收集的血清中验证了这一结果,结果表明 hsa-miR-96 可能在 NSCLC 的发展中起重要作用,并具有作为非侵入性 NSCLC 诊断标志物的巨大潜力。我们基于不同的方法(TargetScan 和 miRanda)预测了潜在的 miRNA 靶 mRNA。根据 miRNA 与靶基因的关系对 miRNA 调控基因进行进一步分类,结果表明 hsa-miR-96 和某些其他 miRNA 倾向于下调 NSCLC 发展过程中靶基因的表达,这些靶基因的表达水平允许 miRNA 与其靶基因直接相互作用。此外,我们还发现 miRNA 调控与高 CpG 岛密度的基因存在显著相关性,这表明 miRNA 可能代表一种调节基本细胞功能和细胞分化的主要调控机制,这种机制可能与 DNA 甲基化在抑制或激活基因表达方面互补。