Ochal-Choińska Aleksandra J, Osuch-Wójcikiewicz Ewa
Department and Chair of Otolaryngology, Medical University of Warsaw, Warsaw, Poland.
Contemp Oncol (Pozn). 2016;20(4):281-6. doi: 10.5114/wo.2016.61847. Epub 2016 Sep 5.
Salivary gland tumours are a group of lesions whose heterogeneity of biological and pathological features is widely reflected in the molecular aspect. This is demonstrated by an increasing number of studies in the field of genetics of these tumours. The aim of this study was to collect the most significant scientific reports on the cytogenetic and molecular data concerning these tumours, which might facilitate the identification of potential biomarkers and therapeutic targets. The analysis covered 71 papers included in the PubMed database. We focused on the most common tumours, such as pleomorphic adenoma, Warthin tumour, mucoepidermoid carcinoma, and others. The aim of this study is to present current knowledge about widely explored genotypic alterations (such as PLAG1 gene in pleomorphic adenoma or MECT1 gene in mucoepidermoid carcinoma), and also about rare markers, like Mena or SOX10 protein, which might also be associated with tumourigenesis and carcinogenesis of these tumours.
涎腺肿瘤是一组病变,其生物学和病理学特征的异质性在分子层面得到广泛体现。这些肿瘤遗传学领域越来越多的研究证明了这一点。本研究的目的是收集有关这些肿瘤细胞遗传学和分子数据的最重要科学报告,这可能有助于识别潜在的生物标志物和治疗靶点。分析涵盖了PubMed数据库中的71篇论文。我们关注的是最常见的肿瘤,如多形性腺瘤、沃辛瘤、黏液表皮样癌等。本研究的目的是介绍目前关于广泛研究的基因型改变(如多形性腺瘤中的PLAG1基因或黏液表皮样癌中的MECT1基因)的知识,以及关于罕见标志物(如Mena或SOX10蛋白)的知识,这些标志物也可能与这些肿瘤的肿瘤发生和癌变有关。