Visani Michela, Acquaviva Giorgia, Fiorino Sirio, Bacchi Reggiani Maria Letizia, Masetti Michele, Franceschi Enrico, Fornelli Adele, Jovine Elio, Fabbri Carlo, Brandes Alba A, Tallini Giovanni, Pession Annalisa, de Biase Dario
Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy Department of Experimental, Diagnostic and Specialty Medicine, School of Medicine, University of Bologna, Bologna, Italy.
J Clin Pathol. 2015 Nov;68(11):859-69. doi: 10.1136/jclinpath-2015-203246. Epub 2015 Aug 27.
Pancreatic tumours are usually very aggressive cancer with a poor prognosis. A limitation of pancreatic imaging techniques is that lesions are often of ambiguous relevance. The inability to achieve a definitive diagnosis based on cytological evaluation of specimens, due to sampling error, paucicellular samples or coexisting inflammation, might lead to delay in clinical management. Given the morbidity associated with pancreatectomy, a proper selection of patients for surgery is fundamental. Many studies have been conducted in order to identify specific markers that could support the early diagnosis of pancreatic lesions, but, to date, none of them allow to diagnose pancreatic cancer with high sensitivity and specificity. MicroRNAs (miRNA) are small non-coding RNAs (19-25 nucleotides) that regulate gene expression interacting with mRNA targets. It is now established that each tissue shows a characteristic miRNA expression pattern that could be modified in association with a number of different diseases including neoplasia. Due to their key role in the regulation of gene expression, in the last years several studies have investigated miRNA tissue-specific expression, quantification and functional analysis to understand their peculiar involvement in cellular processes. The aim of this review is to focus on miRNA expression in pancreatic cancer and their putative role in early characterisation of pancreatic lesions.
胰腺肿瘤通常是侵袭性很强的癌症,预后较差。胰腺成像技术的一个局限性在于,病变的相关性往往不明确。由于取样误差、细胞数量少的样本或并存的炎症,无法根据标本的细胞学评估做出明确诊断,这可能导致临床管理的延迟。鉴于胰腺切除术相关的发病率,正确选择手术患者至关重要。为了确定能够支持胰腺病变早期诊断的特定标志物,已经开展了许多研究,但迄今为止,尚无一种标志物能够以高灵敏度和特异性诊断胰腺癌。微小RNA(miRNA)是小的非编码RNA(19 - 25个核苷酸),通过与mRNA靶标相互作用来调节基因表达。现已证实,每个组织都呈现出一种特征性的miRNA表达模式,这种模式可能会随着包括肿瘤形成在内的多种不同疾病而发生改变。由于它们在基因表达调控中起关键作用,近年来多项研究对miRNA的组织特异性表达、定量和功能分析进行了研究,以了解它们在细胞过程中的特殊作用。本综述的目的是聚焦于胰腺癌中miRNA的表达及其在胰腺病变早期特征描述中的假定作用。