Kiss Orsolya, Tőkés Anna-Mária, Spisák Sándor, Szilágyi Anna, Lippai Norbert, Székely Borbála, Szász A Marcell, Kulka Janina
2nd Department of Pathology, Semmelweis University, Budapest, Hungary,
Pathol Oncol Res. 2015 Jan;21(1):29-44. doi: 10.1007/s12253-014-9770-1. Epub 2014 Sep 21.
Adenoid cystic carcinoma (ACC) is a malignant tumor of the salivary glands but identical tumors can also arise from the breast. Despite their similar histomorphological appearance the salivary gland- and the breast-derived forms differ in their clinical features: while ACC of the salivary glands (sACC) have an aggressive clinical course, the breast-derived form (bACC) shows a very favourable clinical outcome. To date no exact molecular alterations have yet been identified which would explain the diverse clinical features of the ACCs of different origin. In our pilot experiment we investigated the post-transcriptional features of ACC cases by performing microRNA-profiling on 2-2 bACC and sACC tissues and on 1-1 normal breast and salivary gland tissue. By comparing the microRNA-profiles of the investigated samples we identified microRNAs which were expressed differently in bACC and sACC cases according to their normal controls: 7 microRNAs were overexpressed in sACC cases and downexpressed in bACC tumors (let-7b, let-7c, miR-17, miR-20a, miR-24, miR-195, miR-768-3) while 9 microRNAs were downexpressed in sACC cases and overexpressed in bACC tissues (let-7e, miR-23b, miR-27b, miR-193b, miR-320a, miR-320c, miR-768-5p, miR-1280 and miR-1826) relative to their controls. We also identified 8 microRNAs which were only expressed in sACCs and one microRNA (miR-1234) which was only absent in sACC cases. By target predictor online databases potential targets of the these microRNAs were detected to identify genes that may play central role in the diverse clinical outcome of bACC and sACC cases.
腺样囊性癌(ACC)是一种唾液腺恶性肿瘤,但相同的肿瘤也可起源于乳腺。尽管它们具有相似的组织形态学外观,但唾液腺来源和乳腺来源的形式在临床特征上有所不同:唾液腺腺样囊性癌(sACC)具有侵袭性的临床病程,而乳腺来源的形式(bACC)则显示出非常良好的临床结果。迄今为止,尚未确定确切的分子改变来解释不同来源的ACC的不同临床特征。在我们的初步实验中,我们通过对2-2例bACC和sACC组织以及1-1例正常乳腺和唾液腺组织进行微小RNA分析,研究了ACC病例的转录后特征。通过比较所研究样本的微小RNA谱,我们鉴定出根据其正常对照在bACC和sACC病例中表达不同的微小RNA:7种微小RNA在sACC病例中过表达而在bACC肿瘤中低表达(let-7b、let-7c、miR-17、miR-20a、miR-24、miR-195、miR-768-3),而9种微小RNA在sACC病例中低表达而在bACC组织中过表达(let-7e、miR-23b、miR-27b、miR-193b、miR-320a、miR-320c、miR-768-5p、miR-1280和miR-1826)相对于它们的对照。我们还鉴定出8种仅在sACC中表达的微小RNA和一种仅在sACC病例中不存在的微小RNA(miR-1234)。通过在线靶标预测数据库检测这些微小RNA的潜在靶标,以鉴定可能在bACC和sACC病例的不同临床结果中起核心作用的基因。