血液系统恶性肿瘤:遗传学最新进展综述

M. Bendari, S. Sraidi, N. Khoubila
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引用次数: 0

摘要

遗传缺陷在大多数血液系统恶性肿瘤的发病机制中起着重要作用,包括细胞遗传学异常、基因突变和基因表达异常。在过去十年中,由于测序技术的革命发挥了至关重要的作用,我们对血液病遗传学的认识得到了极大的提高。在本章中,我们描述了通常用于阐明染色体畸变的技术,复发性染色体异常的预后影响,以及最近更新的风险分层系统。我们将总结最近在许多血液学疾病中发现的染色体异常,如急性髓性白血病、急性淋巴性白血病、骨髓增生异常综合征、多发性骨髓瘤、骨髓增生性疾病,并阐明它们对临床表型和预后的影响,以及它们在这些疾病的发病机制中的作用。本章的目的是简要概述血液病遗传学的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Haematological Malignancies: Overview of the Recent Progresses in Genetics
Genetic defects play a major role in pathogenesis of the most of haematological malignancies, including cytogenetic abnormalities, gene mutations, and abnormal gene expression. Our knowledge about the genetics of haematological disorders has been dramatically improved during the past decade, due to revolution of sequencing technologies which have played a crucial role. In this chapter, we describe the techniques commonly employed for elucidating chromosomal aberrations, prognostic impact of recurrent chromosomal abnormalities, and recently updated risk stratification systems. We will summarise the chromosomal abnormalities recently identified on many of haematological diseases such acute myeloid leukaemia, acute lymphoid leukaemia, myelodysplasic syndrome, multiple myeloma, meyloproliferative disease and clarify their impacts on clinical phenotype and prognosis, as well as their role in the pathogenesis of these diseases. The aim of this chapter is to provide a brief overview of the recent progresses in haematological diseases genetics.
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