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通过光谱核型分析检测到的晚期神经母细胞瘤肿瘤的不同细胞遗传学途径。

Distinct cytogenetic pathways of advanced-stage neuroblastoma tumors, detected by spectral karyotyping.

作者信息

Stark Batia, Jeison Marta, Bar-Am Irit, Glaser-Gabay Leticia, Mardoukh Jacques, Luria Drorit, Feinmesser Meora, Goshen Yacov, Stein Jerry, Abramov Aya, Zaizov Rina, Yaniv Isaac

机构信息

Cancer Cytogenetic Laboratory, Schneider Children's Medical Center of Israel, Petah Tiqva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Genes Chromosomes Cancer. 2002 Jul;34(3):313-24. doi: 10.1002/gcc.10082.

Abstract

Molecular studies of advanced-stage neuroblastoma (NBL) have revealed a marked genetic heterogeneity. In addition to MYCN amplification and chromosome 1 short-arm deletions/translocations detected by conventional cytogenetics, application of fluorescence in situ hybridization has disclosed a high prevalence of 17q gain, whereas allelotyping and comparative genomic hybridization techniques also have revealed loss of 11q and of other chromosomal material. Using the recently developed technique of spectral karyotyping (SKY), we sought to refine the cytogenetic information, identify hidden recurrent structural chromosomal abnormalities, and compare them to the molecular findings. Thirteen samples of metaphase spreads from 11 patients with advanced-stage NBL were analyzed by SKY. Most of them were found to have complex karyotypes (more than three changes per metaphase) and complex unbalanced rearrangements. Recurrent aberrations leading to 17q gain, deletion of 1p, MYCN amplification, and loss of 11q appeared in 7, 4, 4, and 5 patients, respectively, in simple and complex karyotypes. Chromosome 3 changes and gain of 1q and 7q appeared in 6, 5, and 4 patients, respectively, in complex karyotypes only, reflecting later changes. A strikingly high prevalence of the unbalanced translocation der(11)t(11;17), leading to concomitant 11q loss and 17q gain in 4 patients, delineated a distinct cytogenetic group, none having 1p deletion and/or MYCN amplification. der(11)t(11;17) was associated with complex karyotypes with changes in chromosomes 3 and 7q. The 17q translocations with partners other than 11q were associated with 1p deletion and/or MYCN amplification. The distinct cytogenetic subgroups identified by SKY confirm and extend the recent molecular observations, and suggest that different genes may interact in the der(11)t(11;17) pathway of NBL development and progression.

摘要

晚期神经母细胞瘤(NBL)的分子研究显示出明显的基因异质性。除了通过传统细胞遗传学检测到的MYCN扩增以及1号染色体短臂缺失/易位外,荧光原位杂交技术的应用还揭示了17q增益的高发生率,而等位基因分型和比较基因组杂交技术也发现了11q以及其他染色体物质的缺失。我们使用最近开发的光谱核型分析(SKY)技术,试图完善细胞遗传学信息,识别隐藏的复发性染色体结构异常,并将其与分子研究结果进行比较。对11例晚期NBL患者的13个中期染色体铺片样本进行了SKY分析。发现其中大多数具有复杂核型(每个中期染色体有超过三个变化)和复杂的不平衡重排。导致17q增益、1p缺失、MYCN扩增以及11q缺失的复发性畸变分别出现在7例、4例、4例和5例患者中,核型简单或复杂均有。3号染色体变化以及1q和7q增益仅出现在6例、5例和4例具有复杂核型的患者中,反映出较晚出现的变化。一种不平衡易位der(11)t(11;17)的发生率惊人地高,导致4例患者同时出现11q缺失和17q增益,界定了一个独特的细胞遗传学组,该组中无一例有1p缺失和/或MYCN扩增。der(11)t(11;17)与3号染色体和7q染色体发生变化的复杂核型相关。与11q以外的其他伙伴发生的17q易位与1p缺失和/或MYCN扩增相关。通过SKY鉴定出的不同细胞遗传学亚组证实并扩展了最近的分子研究观察结果,并表明不同基因可能在NBL发生发展的der(11)t(11;17)途径中相互作用。

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