| Literature DB >> 33644035 |
Xiaofang Chen1, Ningyu Li1,2, Jianyu Weng1,2, Xin Du1,2.
Abstract
Myelodysplastic syndrome (MDS) is a group of clonal hematopoietic disorders related to hematopoietic stem and progenitor cell dysfunction. However, therapies that are currently used to target hematopoietic stem cells are not effective. These therapies are able to slow the evolution toward acute myeloid leukemia but cannot eradicate the disease. Mesenchymal stem cells (MSCs) have been identified as one of the main cellular components of the bone marrow microenvironment, which plays an indispensable role in normal hematopoiesis. When functional and regenerative capacities of aging MSCs are diminished, some enter replicative senescence, which promotes inflammation and disease progression. Recent studies that investigated the contribution of bone marrow microenvironment and MSCs to the initiation and progression of the disease have offered new insights into the MDS. This review presents the latest updates on the role of MSCs in the MDS and discusses potential targets for the treatment of MDS.Entities:
Keywords: bone marrow microenvironment; mesenchymal stem cells; myelodysplastic syndrome; senescence; treatment
Year: 2021 PMID: 33644035 PMCID: PMC7905046 DOI: 10.3389/fcell.2020.617466
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X