Division of Hematopathology, Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.
Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19102, USA.
Cold Spring Harb Perspect Med. 2020 Nov 2;10(11):a035444. doi: 10.1101/cshperspect.a035444.
Recurrent genetic aberrations have long been recognized in mature lymphoid leukemias and lymphomas. As conventional karyotypic and molecular cloning techniques evolved in the 1970s and 1980s, multiple cytogenetic aberrations were identified in lymphomas, often balanced translocations that juxtaposed oncogenes to the immunoglobulin (IG) or T-cell receptor (TR) loci, leading to dysregulation. However, genetic characterization and classification of lymphoma by conventional cytogenetic methods is limited by the infrequent occurrence of recurrent karyotypic abnormalities in many lymphoma subtypes and by the frequent difficulty in growing clinical lymphoma specimens in culture to obtain informative karyotypes. As higher-resolution genomic techniques developed, such as array comparative genomic hybridization and fluorescence in situ hybridization, many recurrent copy number changes were identified in lymphomas, and copy number assessment of interphase cells became part of routine clinical practice for a subset of diseases. Platforms to globally examine mRNA expression led to major insights into the biology of several lymphomas, although these techniques have not gained widespread application in routine clinical settings. With the advent of next-generation sequencing (NGS) techniques in the early 2000s, numerous insights into the genetic landscape of lymphomas were obtained. In contrast to the myeloid malignancies, most common lymphomas exhibit an at least somewhat mutationally complex genome, with few single driver mutations in the majority of patients. However, many recurrently mutated pathways have been identified across lymphoma subtypes, informing targeted therapeutic approaches that are beginning to make meaningful changes in the treatment of lymphoma. In addition to the ability to identify possible therapeutic targets, NGS techniques are highly amenable to the tracking of residual lymphoma following therapy, because of the presence of unique genetic "fingerprints" in lymphoma cells due to V(D)-J recombination at the antigen receptor loci. This review will provide an overview of the impact of novel genetic technologies on lymphoma classification, biology, and therapy.
在成熟的淋巴样白血病和淋巴瘤中,反复出现的遗传异常早已为人所知。随着 20 世纪 70 年代和 80 年代常规细胞遗传学和分子克隆技术的发展,在淋巴瘤中鉴定出了多种细胞遗传学异常,这些异常通常是平衡易位,使癌基因与免疫球蛋白(IG)或 T 细胞受体(TR)基因座并列,导致失调。然而,通过常规细胞遗传学方法对淋巴瘤进行遗传特征和分类受到多种局限性的限制,包括许多淋巴瘤亚型中反复出现的核型异常发生率较低,以及临床淋巴瘤标本在培养中经常难以生长以获得有意义的核型。随着更高分辨率的基因组技术的发展,如阵列比较基因组杂交和荧光原位杂交,在淋巴瘤中发现了许多反复出现的拷贝数变化,并且间期细胞的拷贝数评估已成为某些疾病常规临床实践的一部分。全面检查 mRNA 表达的平台为几种淋巴瘤的生物学提供了重要的见解,尽管这些技术尚未在常规临床环境中广泛应用。随着 21 世纪初下一代测序(NGS)技术的出现,人们对淋巴瘤的遗传景观有了更多的了解。与髓系恶性肿瘤不同,大多数常见的淋巴瘤具有至少有些复杂的突变基因组,大多数患者中只有少数单一的驱动突变。然而,已经在淋巴瘤亚型中鉴定出许多反复突变的途径,为靶向治疗方法提供了信息,这些方法开始对淋巴瘤的治疗产生有意义的改变。除了能够识别潜在的治疗靶点外,NGS 技术还非常适合在治疗后追踪残留的淋巴瘤,因为在抗原受体基因座的 V(D)-J 重排过程中,淋巴瘤细胞中存在独特的遗传“指纹”。这篇综述将概述新型遗传技术对淋巴瘤分类、生物学和治疗的影响。