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Clonal hematopoiesis and bone marrow inflammation.
Xie, Xinshu; Su, Meng; Ren, Kehan; Ma, Xuezhen; Lv, Zhiyi; Li, Zhaofeng; Mei, Yang; Ji, Peng.
Afiliación
  • Xie X; School of Biomedical Sciences, Hunan University, Changsha, China.
  • Su M; School of Biomedical Sciences, Hunan University, Changsha, China.
  • Ren K; Department of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois.
  • Ma X; School of Biomedical Sciences, Hunan University, Changsha, China.
  • Lv Z; School of Biomedical Sciences, Hunan University, Changsha, China.
  • Li Z; School of Biomedical Sciences, Hunan University, Changsha, China.
  • Mei Y; School of Biomedical Sciences, Hunan University, Changsha, China; Hunan Provincial Key Laboratory of Medical Virology, Hunan University, Changsha, China. Electronic address: yanmei@hnu.edu.cn.
  • Ji P; Department of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois. Electronic address: peng-ji@fsm.northwestern.edu.
Transl Res ; 255: 159-170, 2023 05.
Article en En | MEDLINE | ID: mdl-36347490
ABSTRACT
Clonal hematopoiesis (CH) occurs in hematopoietic stem cells with increased risks of progressing to hematologic malignancies. CH mutations are predominantly found in aged populations and correlate with an increased incidence of cardiovascular and other diseases. Increased lines of evidence demonstrate that CH mutations are closely related to the inflammatory bone marrow microenvironment. In this review, we summarize the recent advances in this topic starting from the discovery of CH and its mutations. We focus on the most commonly mutated and well-studied genes in CH and their contributions to the innate immune responses and inflammatory signaling, especially in the hematopoietic cells of bone marrow. We also aimed to discuss the interrelationship between inflammatory bone marrow microenvironment and CH mutations. Finally, we provide our perspectives on the challenges in the field and possible future directions to help understand the pathophysiology of CH.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Médula Ósea / Hematopoyesis Clonal Límite: Aged / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Médula Ósea / Hematopoyesis Clonal Límite: Aged / Humans Idioma: En Año: 2023 Tipo del documento: Article