MicroRNA expression profiles in pediatric dysembryoplastic neuroepithelial tumors

被引:17
作者
Braoudaki, M. [1 ,2 ]
Lambrou, G. I. [1 ]
Papadodima, S. A. [3 ]
Stefanaki, K. [4 ]
Prodromou, N. [5 ]
Kanavakis, E. [1 ]
机构
[1] Univ Athens, Univ Res Inst Study & Treatment Childhood Genet &, Aghia Sophia Childrens Hosp, Athens, Greece
[2] Univ Athens, Sch Med, Aghia Sophia Childrens Hosp, Dept Pediat 1,Hematol & Oncol Unit,Choremeio Res, GR-11527 Athens, Greece
[3] Univ Athens, Sch Med, Dept Forens Med & Toxicol, GR-11527 Athens, Greece
[4] Aghia Sophia Childrens Hosp, Dept Pathol, Athens, Greece
[5] Aghia Sophia Childrens Hosp, Dept Neurosurg, Athens, Greece
关键词
Pediatric; Brain tumors; MicroRNA microarrays; qRT-PCR; Biomarkers; ROC curves; DOWN-REGULATION; UP-REGULATION; TARGETS; CLASSIFICATION; CONTRIBUTES; SUPPRESSES; SIGNATURES; CARCINOMA; EPILEPSY;
D O I
10.1007/s12032-015-0719-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Among noncoding RNAs, microRNAs (miRNAs) have been most extensively studied, and their biology has repeatedly been proven critical for central nervous system pathological conditions. The diagnostic value of several miRNAs was appraised in pediatric dysembryoplastic neuroepithelial tumors (DNETs) using miRNA microarrays and receiving operating characteristic curves analyses. Overall, five pediatric DNETs were studied. As controls, 17 samples were used: the FirstChoice Human Brain Reference RNA and 16 samples from deceased children who underwent autopsy and were not present with any brain malignancy. The miRNA extraction was carried out using the mirVANA miRNA Isolation Kit, while the experimental approach included miRNA microarrays covering 1211 miRNAs. Quantitative real-time polymerase chain reaction was performed to validate the expression profiles of miR-1909* and miR-3138 in all samples initially screened with miRNA microarrays. Our findings indicated that miR-3138 might act as a tumor suppressor gene when down-regulated and miR-1909* as a putative oncogenic molecule when up-regulated in pediatric DNETs compared to the control cohort. Subsequently, both miRNA signatures might serve as putative diagnostic biomarkers for pediatric DNETs.
引用
收藏
页码:1 / 7
页数:7
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