SMAD公司
癌症研究
转化生长因子β
髓系白血病
造血
转化生长因子β信号通路
转化生长因子
生物
干细胞
细胞生物学
作者
Nandini Ramachandra,Charan Thej Reddy Vegivinti,Srabani Sahu,Rahul Sanawar,Bianca Rivera-Peña,Sarah Aminov,Ariel Fromowitz,Jinghang Zhang,Fnu Aodengtuya,Kith Pradhan,Rongbao Zhao,Leya Schwartz,Srinivas Alluri,Victor Thiruvananthapuram,Emma Rabinovich,Opeyemi Ajibade,Shanisha Gordon-Mitchell,Aditi Shastri,Marcel A. Deken,Jonathan M. Yingling,Scott Sawyer,Michael Lahn,Amit Verma
标识
DOI:10.1080/10428194.2024.2444479
摘要
Overactivation of the Transforming Growth Factor Beta (TGF-β) pathway is implicated in the pathogenesis of cytopenias in Myelodysplastic syndromes (MDS) and Acute Myeloid Leukemia (AML). IOA-359 and IOA-360 are potent small molecule inhibitors of the TGF-beta Receptor type I kinase (TGF-βRI, also referred to as ALK5, activin receptor-like kinase 5) that abrogate SMAD phosphorylation in hematopoietic cell lines. Both inhibitors were able to inhibit TGF-β mediated gene transcription at specific doses. ALK5 inhibitors abrogated the growth inhibitory effects of TGF-β on healthy hematopoietic stem cells and stimulated hematopoietic differentiation in cell lines and MDS/AML specimens. These data demonstrate preclinical efficacy of two novel ALK5 inhibitors, IOA-359 and IOA-360, in stimulating erythroid differentiation in MDS and AML.
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