克隆造血:恶性和非恶性疾病的融合

IF 4.7 2区 医学 Q1 ONCOLOGY Annual Review of Cancer Biology-Series Pub Date : 2022-01-18 DOI:10.1146/annurev-cancerbio-060121-120026
A. E. Lin, P. Rauch, S. Jaiswal, B. Ebert
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引用次数: 2

摘要

不确定潜能的克隆性造血(CHIP)是一种造血干细胞的体细胞突变导致非血液系统恶性肿瘤个体血细胞克隆扩增的状态。突变基因,包括TET2、DNMT3A、ASXL1、TP53、JAK2和SF3B1,也在髓系恶性肿瘤中反复突变。患有CHIP的个体患癌症的风险增加。此外,CHIP患者的全因死亡率升高,这在很大程度上可归因于心血管疾病,与传统的风险因素无关。这种风险增加的机制可能与突变巨噬细胞引起的炎症增加有关,部分是通过炎症小体激活。这拓宽了我们对慢性疾病如何受到CHIP影响以及炎症在这些疾病中的机制作用的理解。《癌症生物学年度评论》第6卷预计最终在线出版日期为2022年4月。请参阅http://www.annualreviews.org/page/journal/pubdates用于修订估算。
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Clonal Hematopoiesis: Confluence of Malignant and Nonmalignant Diseases
Clonal hematopoiesis of indeterminate potential (CHIP) is a state in which somatic mutations in hematopoietic stem cells lead to clonal expansion of blood cells in individuals without hematologic malignancy. The mutated genes, including TET2, DNMT3A, ASXL1, TP53, JAK2, and SF3B1, are also recurrently mutated in myeloid malignancies. Individuals with CHIP have an increased risk of developing a hematologic cancer. Moreover, individuals with CHIP have an elevated risk of all-cause mortality that is significantly attributable to cardiovascular disease, independent of traditional risk factors. The mechanism for this increased risk is likely linked to increased inflammation driven by mutated macrophages, in part through inflammasome activation. This has broadened our understanding of how chronic diseases are influenced by CHIP and of the mechanistic role of inflammation in these disorders. Expected final online publication date for the Annual Review of Cancer Biology, Volume 6 is April 2022. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
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来源期刊
CiteScore
14.50
自引率
1.30%
发文量
13
期刊介绍: The Annual Review of Cancer Biology offers comprehensive reviews on various topics within cancer research, covering pivotal and emerging areas in the field. As our understanding of cancer's fundamental mechanisms deepens and more findings transition into targeted clinical treatments, the journal is structured around three main themes: Cancer Cell Biology, Tumorigenesis and Cancer Progression, and Translational Cancer Science. The current volume of this journal has transitioned from gated to open access through Annual Reviews' Subscribe to Open program, ensuring all articles are published under a CC BY license.
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