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分子细胞遗传学:实体瘤与白血病

Molecular cytogenetics: solid tumors and leukemia.

作者信息

Gray J W, Pallavicini M G

机构信息

Department of Laboratory Medicine, University of California, San Francisco 94143-0808.

出版信息

Blood Cells. 1993;19(3):677-83; discussion 687-9.

PMID:8018948
Abstract

Acute leukemia represents one of the best-studied malignancies. Consequently, numerous dogmas have evolved over the years. One dogma to which we subscribe is that leukemia is a genetic disease and that the behavior of leukemic cells and their response to therapy is determined largely by their genetic characteristics. The relative ease of metaphase generation and culture of single leukemic cells, well-defined morphologic criteria, and availability of phenotyping reagents has contributed to a wealth of information about the karyotypic, genetic, and functional properties of these cells. Nevertheless, establishment of genotype-phenotype relationships has been particularly elusive. The genetic evolution of leukemias and the consequences of specific aberrations remains to be determined. We describe the power of new molecular cytogenetic tools, fluorescence in situ hybridization, and comparative genomic hybridization to measure the genetic evolution of leukemic cells. Lessons learned from application of these techniques to solid tumors and speculations about similar approaches to analysis of leukemia are addressed.

摘要

急性白血病是研究最为深入的恶性肿瘤之一。因此,多年来形成了众多的教条。我们认同的一个教条是,白血病是一种遗传性疾病,白血病细胞的行为及其对治疗的反应在很大程度上由其遗传特征决定。单个白血病细胞中期的生成和培养相对容易,形态学标准明确,且有表型分析试剂可用,这些都为获取有关这些细胞的核型、遗传和功能特性的丰富信息做出了贡献。然而,基因型 - 表型关系的建立一直特别难以捉摸。白血病的遗传演变以及特定畸变的后果仍有待确定。我们描述了新的分子细胞遗传学工具、荧光原位杂交和比较基因组杂交在测量白血病细胞遗传演变方面的作用。还讨论了将这些技术应用于实体瘤所吸取的经验教训以及对白血病分析类似方法的推测。

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