Back to Search Start Over

BATF promotes extramedullary infiltration through TGF-β1/Smad/MMPs axis in acute myeloid leukemia.

Authors :
Zhang R
Miao J
Zhai M
Liu R
Li F
Xu X
Huang L
Wang T
Yang R
Yang R
Wang Y
He A
Wang J
Source :
Molecular carcinogenesis [Mol Carcinog] 2024 Jun; Vol. 63 (6), pp. 1146-1159. Date of Electronic Publication: 2024 Mar 13.
Publication Year :
2024

Abstract

Acute myeloid leukemia (AML) is one of the most prevalent types of leukemia and is challenging to cure for most patients. Basic Leucine Zipper ATF-Like Transcription Factor (BATF) has been reported to participate in the development and progression of numerous tumors. However, its role in AML is largely unknown. In this study, the expression and prognostic value of BATF were examined in AML. Our results demonstrated that BATF expression was upregulated in AML patients, which was significantly correlated with poor clinical characteristics and survival. Afterward, functional experiments were performed after knocking down or overexpressing BATF by transfecting small interfering RNAs and overexpression plasmids into AML cells. Our findings revealed that BATF promoted the migratory and invasive abilities of AML cells in vitro and in vivo. Moreover, the target genes of BATF were searched from databases to explore the binding of BATF to the target gene using ChIP and luciferase assays. Notably, our observations validated that BATF is bound to the promoter region of TGF-β1, which could transcriptionally enhance the expression of TGF-β1 and activate the TGF-β1/Smad/MMPs signaling pathway. In summary, our study established the aberrantly high expression of BATF and its pro-migratory function via the TGF-β1-Smad2/3-MMP2/9 axis in AML, which provides novel insights into extramedullary infiltration of AML.<br /> (© 2024 The Authors. Molecular Carcinogenesis published by Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1098-2744
Volume :
63
Issue :
6
Database :
MEDLINE
Journal :
Molecular carcinogenesis
Publication Type :
Academic Journal
Accession number :
38477642
Full Text :
https://doi.org/10.1002/mc.23715