Resistance to inflammation underlies enhanced fitness in clonal hematopoiesis

Author:

Avagyan S.1ORCID,Henninger J. E.2ORCID,Mannherz W. P.3ORCID,Mistry M.4ORCID,Yoon J.4ORCID,Yang S.5ORCID,Weber M. C.5,Moore J. L.5ORCID,Zon L. I.56ORCID

Affiliation:

1. Dana-Farber/Boston Children’s Cancer and Blood Disorders Center, Boston, MA, USA.

2. Whitehead Institute for Biomedical Research, Cambridge, MA, USA.

3. Harvard Medical School, Boston, MA, USA.

4. Harvard Chan Bioinformatics Core, Boston, MA, USA.

5. Boston Children’s Hospital, Boston, MA, USA.

6. Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA.

Abstract

Colorful clones in the blood Stem cells in regenerating tissues such as the blood can acquire mutations that enable a growth advantage, increasing the chance of developing cancer. It is unclear how such diverse mutations promote clonal fitness. Avagyan et al . generated a platform in zebrafish to label clones with unique hues while inducing mutations in genes implicated in human blood disorders. Mutations in some genes caused clones to expand over time, resulting in clonal dominance. Progenitors in the dominant clone expressed anti-inflammatory factors to resist the inflammatory environment produced by their own mature progeny, leading to a self-perpetuating cycle promoting clonal fitness. Targeting these resistance pathways may be used to abate clonal hematopoiesis and prevent its associated pathology. —BAP

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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