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人类胶质瘤遗传物质增减的分子细胞遗传学定量分析

Molecular cytogenetic quantitation of gains and losses of genetic material from human gliomas.

作者信息

Feuerstein B G, Mohapatra G

机构信息

Department of Laboratory Medicine, School of Medicine, University of California, San Francisco 94143, USA.

出版信息

J Neurooncol. 1995;24(1):47-55. doi: 10.1007/BF01052658.

Abstract

The unregulated growth that is characteristic of human malignant gliomas is accompanied by, and may result from, losses and/or gains of genetic material. Understanding the mechanisms that underlie how particular genetic aberrations cause dysfunctional growth will help elucidate the pathogenesis of this disease. Two techniques are proving useful in evaluating the clinical relevance of specific genetic aberrations in malignant gliomas. Fluorescence in situ hybridization (FISH) permits direct visualization of gains and losses of genetic material in single cells and quantitation of cellular subpopulations that have particular genetic aberrations. Comparative genomic hybridization can identify regions of genetic gain and loss in tumor DNA.

摘要

人类恶性胶质瘤的特征性无序生长伴随着遗传物质的缺失和/或增加,并且可能由其导致。了解特定基因畸变导致功能失调性生长的潜在机制将有助于阐明这种疾病的发病机制。两种技术在评估恶性胶质瘤中特定基因畸变的临床相关性方面已证明是有用的。荧光原位杂交(FISH)可以直接观察单个细胞中遗传物质的增减,并对具有特定基因畸变的细胞亚群进行定量分析。比较基因组杂交可以识别肿瘤DNA中基因增加和缺失的区域。

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