Lynette M. Sholl, Janina Longtine, Frank C. Kuo
{"title":"Molecular Analysis of Gene Rearrangements and Mutations in Acute Leukemias and Myeloid Neoplasms","authors":"Lynette M. Sholl, Janina Longtine, Frank C. Kuo","doi":"10.1002/cphg.31","DOIUrl":null,"url":null,"abstract":"<p>A subset of acute leukemias and other myeloid neoplasms contains specific genetic alterations, many of which are associated with unique clinical and pathologic features. These alterations include chromosomal rearrangements leading to oncogenic fusion proteins or alteration of gene expression by juxtaposing oncogenes to enhancer elements, as well as mutations leading to aberrant activation of a variety of proteins critical to hematopoietic progenitor cell proliferation and differentiation. Molecular analysis is central to diagnosis and clinical management of leukemias, permitting genetic confirmation of a clinical and histologic impression, providing prognostic and predictive information, and facilitating detection of minimal residual disease. This unit will outline approaches to the molecular diagnosis of the most frequent and clinically relevant genetic alterations in acute leukemias and myeloid neoplasms. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":40007,"journal":{"name":"Current Protocols in Human Genetics","volume":"92 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cphg.31","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Human Genetics","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cphg.31","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
Abstract
A subset of acute leukemias and other myeloid neoplasms contains specific genetic alterations, many of which are associated with unique clinical and pathologic features. These alterations include chromosomal rearrangements leading to oncogenic fusion proteins or alteration of gene expression by juxtaposing oncogenes to enhancer elements, as well as mutations leading to aberrant activation of a variety of proteins critical to hematopoietic progenitor cell proliferation and differentiation. Molecular analysis is central to diagnosis and clinical management of leukemias, permitting genetic confirmation of a clinical and histologic impression, providing prognostic and predictive information, and facilitating detection of minimal residual disease. This unit will outline approaches to the molecular diagnosis of the most frequent and clinically relevant genetic alterations in acute leukemias and myeloid neoplasms. © 2017 by John Wiley & Sons, Inc.
急性白血病和髓系肿瘤基因重排和突变的分子分析
急性白血病和其他髓系肿瘤的一个子集包含特定的遗传改变,其中许多与独特的临床和病理特征有关。这些改变包括染色体重排导致致癌融合蛋白或通过将致癌基因与增强元件并列而导致基因表达改变,以及导致对造血祖细胞增殖和分化至关重要的各种蛋白质异常激活的突变。分子分析对白血病的诊断和临床管理至关重要,它允许对临床和组织学印象进行遗传确认,提供预后和预测信息,并促进微小残留疾病的检测。本单元将概述急性白血病和髓系肿瘤中最常见和临床相关的遗传改变的分子诊断方法。©2017 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。