Westbrook C A, Hsu W T, Chyna B, Litvak D, Raza A, Horrigan S K
Section of Hematology/Oncology, Department of Medicine, University of Illinois at Chicago, 60607-7173, USA.
Br J Haematol. 2000 Sep;110(4):847-55. doi: 10.1046/j.1365-2141.2000.02285.x.
Deletions of chromosome 5, del(5q), are frequently observed in myelodysplasia (MDS). We evaluated molecular detection of loss of heterozygosity (LOH) as a diagnostic method to detect del(5q) in a series of 60 MDS cases at a single institution. LOH was compared to cytogenetics on the same clinical specimen, resolving ambiguous cases by fluorescent in situ hybridization (FISH) and additional LOH. There was poor concordance between molecular and cytogenetic results, but most discrepancies could be resolved by FISH and additional LOH. Molecular analysis was of low sensitivity because most cases contained a relatively high proportion of cells without del(5q), but it was accurate, while cytogenetics overestimated the proportion of cells with del(5q) and failed to detect some cases with complex rearrangements. Minor clones were detected both by FISH and LOH. Overall, we found an incidence of 23% (14 of 60 cases) for del(5q) in MDS. The results also suggest that there is a high degree of genetic heterogeneity in the cellular population of MDS. Although del(5q) is common in MDS, it may not be present in all cells, leading to diagnostic challenges.
5号染色体缺失(del(5q))在骨髓增生异常综合征(MDS)中经常可见。我们评估了杂合性缺失(LOH)的分子检测作为一种诊断方法,用于在一家机构的60例MDS病例系列中检测del(5q)。将LOH与同一临床标本的细胞遗传学结果进行比较,通过荧光原位杂交(FISH)和额外的LOH来解决不明确的病例。分子和细胞遗传学结果之间的一致性较差,但大多数差异可以通过FISH和额外的LOH来解决。分子分析的敏感性较低,因为大多数病例中含有相对较高比例的无del(5q)细胞,但它是准确的,而细胞遗传学高估了有del(5q)细胞的比例,并且未能检测到一些具有复杂重排的病例。FISH和LOH均检测到了小克隆。总体而言,我们发现MDS中del(5q)的发生率为23%(60例中的14例)。结果还表明,MDS细胞群体中存在高度的遗传异质性。虽然del(5q)在MDS中很常见,但它可能并非存在于所有细胞中,这导致了诊断上的挑战。