Zhang Xiaoying, Cairns Murray, Rose Barbara, O'Brien Christopher, Shannon Kerwin, Clark Jonathan, Gamble Jennifer, Tran Nham
The Sydney Head and Neck Cancer Institute, Sydney Cancer Centre, Royal Prince Alfred Hospital and University of Sydney, Sydney, New South Wales, Australia.
Int J Cancer. 2009 Jun 15;124(12):2855-63. doi: 10.1002/ijc.24298.
Genome-wide microRNA (miRNA) expression profiling of salivary gland pleomorphic adenomas revealed a distinct expression signature consisting largely of upregulated miRNAs compared with matched normal tissue. Microarray data were confirmed by quantitative real time RT-PCR (q-RTPCR). Five miRNA genes upregulated in the tumours were found in close proximity to fragile sites and/or cancer associated genomic regions. Interestingly, q-RTPCR revealed an increase in the expression of components of the miRNA processing machinery (Dicer, Drosha, DGCR8 and p68) in tumours suggesting that the deregulation of miRNA expression may result from increased miRNA biogenesis. Target gene prediction analysis of the altered miRNAs indicated that genes in a number of signalling pathways important in tumourigenesis including WNT, MAPK and JAK-STAT were overrepresented. Significantly, the oncogene PLAG1 was overexpressed in our cohort and may be potentially regulated by these miRNAs. This is the first study to examine changes in the miRNA milieu in pleomorphic adenoma, the most common salivary gland tumour. This study has demonstrated an upregulation of both miRNAs genes and an upregulation of the miRNA processing machinery. These changes may be potential underlying mechanisms for the development of these benign tumours.
涎腺多形性腺瘤的全基因组微小RNA(miRNA)表达谱分析显示,与配对的正常组织相比,其具有明显的表达特征,主要由上调的miRNA组成。微阵列数据通过定量实时逆转录PCR(q-RTPCR)得到证实。在肿瘤中上调的5个miRNA基因被发现紧邻脆性位点和/或癌症相关基因组区域。有趣的是,q-RTPCR显示肿瘤中miRNA加工机制(Dicer、Drosha、DGCR8和p68)的成分表达增加,这表明miRNA表达失调可能是由于miRNA生物合成增加所致。对改变的miRNA进行靶基因预测分析表明,在肿瘤发生中重要的一些信号通路(包括WNT、MAPK和JAK-STAT)中的基因过度富集。值得注意的是,癌基因PLAG1在我们的队列中过表达,可能受这些miRNA的潜在调控。这是第一项研究多形性腺瘤(最常见的涎腺肿瘤)中miRNA环境变化的研究。该研究证明了miRNA基因的上调以及miRNA加工机制的上调。这些变化可能是这些良性肿瘤发生发展的潜在机制。