Clonal hematopoiesis and bone marrow inflammation
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 demonstra...
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Veröffentlicht in: | Translational research : the journal of laboratory and clinical medicine 2023-05, Vol.255, p.159-170 |
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container_title | Translational research : the journal of laboratory and clinical medicine |
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creator | Xie, Xinshu Su, Meng Ren, Kehan Ma, Xuezhen Lv, Zhiyi Li, Zhaofeng Mei, Yang Ji, Peng |
description | 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. |
doi_str_mv | 10.1016/j.trsl.2022.11.004 |
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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.</description><identifier>ISSN: 1931-5244</identifier><identifier>EISSN: 1878-1810</identifier><identifier>DOI: 10.1016/j.trsl.2022.11.004</identifier><identifier>PMID: 36347490</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Bone Marrow ; Clonal Evolution ; Clonal Hematopoiesis - genetics ; Hematopoiesis - genetics ; Humans ; Inflammation - genetics ; Mutation</subject><ispartof>Translational research : the journal of laboratory and clinical medicine, 2023-05, Vol.255, p.159-170</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. 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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.</description><subject>Aged</subject><subject>Bone Marrow</subject><subject>Clonal Evolution</subject><subject>Clonal Hematopoiesis - genetics</subject><subject>Hematopoiesis - genetics</subject><subject>Humans</subject><subject>Inflammation - genetics</subject><subject>Mutation</subject><issn>1931-5244</issn><issn>1878-1810</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMotlb_gAfZo5ddM0mazYIXKX5BwYueQ5rMYsrupiZbxX9vSqtHTzMDz7zMPIRcAq2AgrxZV2NMXcUoYxVARak4IlNQtSpBAT3OfcOhnDMhJuQspXUGZEPFKZlwyUUtGjolsOjCYLriHXszhk3wmHwqzOCKVRiw6E2M4avwQ9uZPhM-DOfkpDVdwotDnZG3h_vXxVO5fHl8XtwtSysoHUsugdnWCcuRGwG2UTWKPLdKKQES65V0NWPGcVRmbowybQNi1SrqwFLH-Ixc73M3MXxsMY2698li15kBwzZpVnMhQcqGZ5TtURtDShFbvYk-n_6tgeqdKr3WO1V6p0oD6GwiL10d8rerHt3fyq-bDNzuAcxffnqMOlmPg0XnI9pRu-D_y_8BfYV6Rw</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Xie, Xinshu</creator><creator>Su, Meng</creator><creator>Ren, Kehan</creator><creator>Ma, Xuezhen</creator><creator>Lv, Zhiyi</creator><creator>Li, Zhaofeng</creator><creator>Mei, Yang</creator><creator>Ji, Peng</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8849-3625</orcidid></search><sort><creationdate>202305</creationdate><title>Clonal hematopoiesis and bone marrow inflammation</title><author>Xie, Xinshu ; Su, Meng ; Ren, Kehan ; Ma, Xuezhen ; Lv, Zhiyi ; Li, Zhaofeng ; Mei, Yang ; Ji, Peng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-3612cfd4c3e3a41c987e4fd4f888416e7b6d722ad3e8a5aa8af914bf80d1c0d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aged</topic><topic>Bone Marrow</topic><topic>Clonal Evolution</topic><topic>Clonal Hematopoiesis - genetics</topic><topic>Hematopoiesis - genetics</topic><topic>Humans</topic><topic>Inflammation - genetics</topic><topic>Mutation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xie, Xinshu</creatorcontrib><creatorcontrib>Su, Meng</creatorcontrib><creatorcontrib>Ren, Kehan</creatorcontrib><creatorcontrib>Ma, Xuezhen</creatorcontrib><creatorcontrib>Lv, Zhiyi</creatorcontrib><creatorcontrib>Li, Zhaofeng</creatorcontrib><creatorcontrib>Mei, Yang</creatorcontrib><creatorcontrib>Ji, Peng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Translational research : the journal of laboratory and clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xie, Xinshu</au><au>Su, Meng</au><au>Ren, Kehan</au><au>Ma, Xuezhen</au><au>Lv, Zhiyi</au><au>Li, Zhaofeng</au><au>Mei, Yang</au><au>Ji, Peng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clonal hematopoiesis and bone marrow inflammation</atitle><jtitle>Translational research : the journal of laboratory and clinical medicine</jtitle><addtitle>Transl Res</addtitle><date>2023-05</date><risdate>2023</risdate><volume>255</volume><spage>159</spage><epage>170</epage><pages>159-170</pages><issn>1931-5244</issn><eissn>1878-1810</eissn><abstract>Clonal hematopoiesis (CH) occurs in hematopoietic stem cells with increased risks of progressing to hematologic malignancies. 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subjects | Aged Bone Marrow Clonal Evolution Clonal Hematopoiesis - genetics Hematopoiesis - genetics Humans Inflammation - genetics Mutation |
title | Clonal hematopoiesis and bone marrow inflammation |
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