克隆性造血、炎症和血液系统恶性肿瘤。

IF 28.4 1区 医学 Q1 PATHOLOGY
Rashmi Kanagal-Shamanna, David B Beck, Katherine R Calvo
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引用次数: 0

摘要

体细胞或获得性突变是合子后的遗传变异,可以发生在任何组织中。这些突变在衰老过程中积累,通常与恶性过程有关。过去几年的巨大进步使人们对体细胞突变在良性和恶性年龄相关疾病中的作用有了更深入的了解。在这里,我们回顾了血液中积累的体细胞突变及其与疾病状态的联系,特别关注炎症性疾病和骨髓增生异常综合征。我们包括克隆性造血(CH)的定义,以及这些突变的起源和意义的概述。此外,我们强调具有重叠炎症的躯体疾病和CH以外的血液系统疾病,包括阵发性夜间血红蛋白尿和再生障碍性贫血,重点关注VEXAS(液泡、E1酶、X-连锁、自身炎症、躯体)综合征。最后,我们对体细胞突变在临床血液学、病理学及其他方面的意义提供了一个实用的观点。《病理学年度评论:疾病机制》第19卷预计最终在线出版日期为2024年1月。请参阅http://www.annualreviews.org/page/journal/pubdates用于修订估算。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clonal Hematopoiesis, Inflammation, and Hematologic Malignancy.

Somatic or acquired mutations are postzygotic genetic variations that can occur within any tissue. These mutations accumulate during aging and have classically been linked to malignant processes. Tremendous advancements over the past years have led to a deeper understanding of the role of somatic mutations in benign and malignant age-related diseases. Here, we review the somatic mutations that accumulate in the blood and their connection to disease states, with a particular focus on inflammatory diseases and myelodysplastic syndrome. We include a definition of clonal hematopoiesis (CH) and an overview of the origins and implications of these mutations. In addition, we emphasize somatic disorders with overlapping inflammation and hematologic disease beyond CH, including paroxysmal nocturnal hemoglobinuria and aplastic anemia, focusing on VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome. Finally, we provide a practical view of the implications of somatic mutations in clinical hematology, pathology, and beyond.

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来源期刊
CiteScore
62.60
自引率
0.00%
发文量
40
期刊介绍: The Annual Review of Pathology: Mechanisms of Disease is a scholarly journal that has been published since 2006. Its primary focus is to provide a comprehensive overview of recent advancements in our knowledge of the causes and development of significant human diseases. The journal places particular emphasis on exploring the current and evolving concepts of disease pathogenesis, as well as the molecular genetic and morphological changes associated with various diseases. Additionally, the journal addresses the clinical significance of these findings. In order to increase accessibility and promote the broad dissemination of research, the current volume of the journal has transitioned from a gated subscription model to an open access format. This change has been made possible through the Annual Reviews' Subscribe to Open program, which allows all articles published in this volume to be freely accessible to readers. As part of this transition, all articles in the journal are published under a Creative Commons Attribution (CC BY) license, which encourages open sharing and use of the research.
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