Loss of Chromosome 1p/19q in Oligodendroglial Tumors: Refinement of Chromosomal Critical Regions and Evaluation of Internexin Immunostaining as a Surrogate Marker

被引:23
作者
Buckley, Patrick G. [1 ,2 ,3 ]
Alcock, Leah [2 ,3 ]
Heffernan, Josephine [4 ]
Woods, Jack [4 ]
Brett, Francesca [4 ]
Stallings, Raymond L. [2 ,3 ]
Farrell, Michael A. [4 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Mol & Cellular Therapeut, Dublin 2, Ireland
[2] Royal Coll Surg Ireland, Dept Canc Genet, York House, Ireland
[3] Our Ladys Childrens Hosp, Natl Childrens Res Ctr, Crumlin, Ireland
[4] Beaumont Hosp, Dept Neuropathol, Dublin 9, Ireland
基金
爱尔兰科学基金会;
关键词
aCGH; Deletion; Internexin; Oligodendroglioma; Prognosis; COMPARATIVE GENOMIC HYBRIDIZATION; ALPHA-INTERNEXIN; EXPRESSION; 1P; 19Q; PREDICTORS; PROGNOSIS; SURVIVAL; FAMILY; GENE;
D O I
10.1097/NEN.0b013e31820c765b
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Loss of chromosome 1p/19q in oligodendrogliomas represents a powerful predictor of good prognosis. Expression of internexin (INA), a neuronal specific intermediate filament protein, has recently been proposed as a surrogate marker for 1p/19q deletion based on the high degree of correlation between both parameters in oligodendrogliomas. The aim of this study was to assess further the diagnostic utility of INA expression in a set of genetically well-characterized oligodendrogliomas. On the basis of a conservative approach for copy number determination, using both comparative genomic hybridization and fluorescent in situ hybridization, INA expression as a surrogate marker for 1p/19q loss had both reduced specificity (80%) and sensitivity (79%) compared with respective values of 86% and 96% reported in the previous report. The histologic interpretation and diagnostic value of INA expression in oligodendrogliomas should therefore be assessed with greater caution when compared with 1p/19q DNA copy number analysis. In addition, DNA copy number aberrations of chromosomes 10, 16, and 17 were detected exclusively in 1p/ 19q codeleted samples, suggesting that other regions of the genome may contribute to the 1p/19q-deleted tumor phenotype in these samples.
引用
收藏
页码:177 / 182
页数:6
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