松果体区乳头状肿瘤:一种独特的分子实体。
Papillary Tumor of the Pineal Region: A Distinct Molecular Entity.
作者信息
Heim Stephanie, Sill Martin, Jones David T W, Vasiljevic Alexandre, Jouvet Anne, Fèvre-Montange Michelle, Wesseling Pieter, Beschorner Rudi, Mittelbronn Michel, Kohlhof Patricia, Hovestadt Volker, Johann Pascal, Kool Marcel, Pajtler Kristian W, Korshunov Andrey, Ruland Vincent, Sperveslage Jan, Thomas Christian, Witt Hendrik, von Deimling Andreas, Paulus Werner, Pfister Stefan M, Capper David, Hasselblatt Martin
机构信息
Institute of Neuropathology, University Hospital Münster, Münster, Germany.
Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
出版信息
Brain Pathol. 2016 Mar;26(2):199-205. doi: 10.1111/bpa.12282. Epub 2015 Jul 30.
Papillary tumor of the pineal region (PTPR) is a neuroepithelial brain tumor, which might pose diagnostic difficulties and recurs often. Little is known about underlying molecular alterations. We therefore investigated chromosomal copy number alterations, DNA methylation patterns and mRNA expression profiles in a series of 24 PTPRs. Losses of chromosome 10 were identified in all 13 PTPRs examined. Losses of chromosomes 3 and 22q (54%) as well as gains of chromosomes 8p (62%) and 12 (46%) were also common. DNA methylation profiling using Illumina 450k arrays reliably distinguished PTPR from ependymomas and pineal parenchymal tumors of intermediate differentiation. PTPR could be divided into two subgroups based on methylation pattern, PTPR group 2 showing higher global methylation and a tendency toward shorter progression-free survival (P = 0.06). Genes overexpressed in PTPR as compared with ependymal tumors included SPDEF, known to be expressed in the rodent subcommissural organ. Notable SPDEF protein expression was encountered in 15/19 PTPRs as compared with only 2/36 ependymal tumors, 2/19 choroid plexus tumors and 0/23 samples of other central nervous system (CNS) tumor entities. In conclusion, PTPRs show typical chromosomal alterations as well as distinct DNA methylation and expression profiles, which might serve as useful diagnostic tools.
松果体区乳头状瘤(PTPR)是一种神经上皮性脑肿瘤,可能会造成诊断困难且常复发。对其潜在的分子改变了解甚少。因此,我们研究了24例PTPR的染色体拷贝数改变、DNA甲基化模式和mRNA表达谱。在所检测的全部13例PTPR中均发现有10号染色体缺失。3号染色体和22q染色体缺失(54%)以及8p染色体(62%)和12号染色体(46%)增加也很常见。使用Illumina 450k芯片进行的DNA甲基化分析能够可靠地将PTPR与室管膜瘤和中间分化的松果体实质肿瘤区分开来。根据甲基化模式,PTPR可分为两个亚组,PTPR第2组显示出更高的整体甲基化水平以及无进展生存期较短的趋势(P = 0.06)。与室管膜瘤相比,PTPR中过表达的基因包括SPDEF,已知该基因在啮齿动物的联合下器官中表达。在19例PTPR中有15例检测到显著的SPDEF蛋白表达,相比之下,36例室管膜瘤中只有2例、19例脉络丛肿瘤中只有2例以及23例其他中枢神经系统(CNS)肿瘤实体样本中均未检测到。总之,PTPR显示出典型的染色体改变以及独特的DNA甲基化和表达谱,这些可能是有用的诊断工具。
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