Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Signaling pathways and bone marrow microenvironment in myelodysplastic neoplasms

Title: Signaling pathways and bone marrow microenvironment in myelodysplastic neoplasms
Authors: Ceneri, Eleonora; De Stefano, Alessia; Casalin, Irene; Finelli, Carlo; Curti, Antonio; Paolini, Stefania; Parisi, Sarah; Ardizzoia, Federica; Cristiano, Gianluca; Boultwood, Jaqueline; McCubrey, James A; Suh, Pann-Ghill; Ramazzotti, Giulia; Fiume, Roberta; Ratti, Stefano; Manzoli, Lucia; Cocco, Lucio; Follo, Matilde Y
Contributors: Ceneri, Eleonora; De Stefano, Alessia; Casalin, Irene; Finelli, Carlo; Curti, Antonio; Paolini, Stefania; Parisi, Sarah; Ardizzoia, Federica; Cristiano, Gianluca; Boultwood, Jaqueline; Mccubrey, James A; Suh, Pann-Ghill; Ramazzotti, Giulia; Fiume, Roberta; Ratti, Stefano; Manzoli, Lucia; Cocco, Lucio; Follo, Matilde Y
Publication Year: 2025
Collection: IRIS Università degli Studi di Bologna (CRIS - Current Research Information System)
Subject Terms: Bone marrow microenvironment; Myelodysplastic neoplasm; NF-κB signaling; Notch signaling; Phosphoinositide signaling; TGF-β signaling
Description: Key signaling pathways within the Bone Marrow Microenvironment (BMM), such as Notch, Phosphoinositide-Specific Phospholipase C (PI-PLCs), Transforming Growth Factor β (TGF-β), and Nuclear Factor Kappa B (NF-κB), play a vital role in the progression of Myelodysplastic Neoplasms (MDS). Among the various BMM cell types, Mesenchymal Stromal Cells (MSCs) are particularly central to these pathways. While these signaling routes can independently affect both MSCs and Hematopoietic Stem Cells (HSCs), they most importantly alter the dynamics of their interactions, leading to abnormal changes in survival, differentiation, and quiescence. Notch and PI-PLC signaling facilitate intercellular communication, TGF-β promotes quiescence and suppresses hematopoiesis, and NF-κB-driven inflammatory responses foster an environment detrimental to normal hematopoiesis. This review highlights the role of these pathways within the MDS microenvironment, driving the development and progression of the disease and paving the way for new possible therapeutic strategies.
Document Type: article in journal/newspaper
File Description: STAMPA
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/39648082; info:eu-repo/semantics/altIdentifier/wos/WOS:001428211600001; volume:95; firstpage:1; lastpage:6; numberofpages:6; journal:ADVANCES IN BIOLOGICAL REGULATION; https://hdl.handle.net/11585/1006980
DOI: 10.1016/j.jbior.2024.101071
Availability: https://hdl.handle.net/11585/1006980; https://doi.org/10.1016/j.jbior.2024.101071
Rights: info:eu-repo/semantics/openAccess ; license:Licenza per Accesso Aperto. Creative Commons Attribuzione (CCBY) ; license uri:iris.PUB15
Accession Number: edsbas.6F12D2A1
Database: BASE