Adam P, Steinlein C, Schmid M, Haralambieva E, Stocklein H, Leich E, Rosenwald A, Muller-Hermelink H K, Ott G
Institute of Pathology, University of Wurzburg, Wurzburg, Germany.
Cytogenet Genome Res. 2006;114(3-4):274-8. doi: 10.1159/000094213.
Cytogenetic chromosome analysis by classical G-banding was supplemented by spectral karyotyping (SKY) in 12 cases of diffuse large B-cell lymphoma (DLBL). SKY is a fluorescence in-situ-based, genome-wide screening technique allowing identification of genetic material even in highly condensed metaphase chromosomes of poor morphology. By simultaneous hybridization of whole chromosome painting probes onto tumor chromosome spreads genetic rearrangements are visualized permitting the clarification of even complex karyotype alterations and the identification of genetic material of previously unknown origin, so-called marker chromosomes. Taking the SKY results into account, we reevaluated the G-banding karyotypes initially carried out, thus generating a more precise karyotype in ten of twelve (83%) cases investigated. In particular, thirteen chromosomal rearrangements not correctly recognized by classical cytogenetics were identified, the genetic origin of seven marker chromosomes was elucidated and three structural genetic rearrangements were redefined. We found SKY to be a valuable technique to establish a definite karyotype in addition to classical cytogenetics.
在12例弥漫性大B细胞淋巴瘤(DLBL)中,除了经典的G显带细胞遗传学染色体分析外,还采用了光谱核型分析(SKY)。SKY是一种基于荧光原位的全基因组筛选技术,即使在形态不佳的高度浓缩中期染色体中也能识别遗传物质。通过将全染色体涂染探针同时杂交到肿瘤染色体涂片上,可使基因重排可视化,从而能够阐明甚至复杂的核型改变,并识别出先前未知来源的遗传物质,即所谓的标记染色体。考虑到SKY的结果,我们重新评估了最初进行的G显带核型,从而在所研究的12例病例中的10例(83%)中生成了更精确的核型。特别是,识别出了13种经典细胞遗传学未正确识别的染色体重排,阐明了7条标记染色体的遗传起源,并重新定义了3种结构基因重排。我们发现,除了经典细胞遗传学外,SKY是建立明确核型的一项有价值的技术。