Targeting S100A9 protein affects mTOR-ER stress signaling and increases venetoclax sensitivity in Acute Myeloid Leukemia.
Rong FanHatice SatilmisNiels VandewalleEmma VerheyeElke De BruyneEline MenuNathan De BeuleAnn De BeckerGamze AtesAnn MassieTessa KerreMarie TörngrenHelena ErikssonKarin VanderkerkenKarine BreckpotKen MaesKim De VeirmanPublished in: Blood cancer journal (2023)
Acute Myeloid Leukemia (AML) is a heterogeneous disease with limited treatment options and a high demand for novel targeted therapies. Since myeloid-related protein S100A9 is abundantly expressed in AML, we aimed to unravel the therapeutic impact and underlying mechanisms of targeting both intracellular and extracellular S100A9 protein in AML cell lines and primary patient samples. S100A9 silencing in AML cell lines resulted in increased apoptosis and reduced AML cell viability and proliferation. These therapeutic effects were associated with a decrease in mTOR and endoplasmic reticulum stress signaling. Comparable results on AML cell proliferation and mTOR signaling could be observed using the clinically available S100A9 inhibitor tasquinimod. Interestingly, while siRNA-mediated targeting of S100A9 affected both extracellular acidification and mitochondrial metabolism, tasquinimod only affected the mitochondrial function of AML cells. Finally, we found that S100A9-targeting approaches could significantly increase venetoclax sensitivity in AML cells, which was associated with a downregulation of BCL-2 and c-MYC in the combination group compared to single agent therapy. This study identifies S100A9 as a novel molecular target to treat AML and supports the therapeutic evaluation of tasquinimod in venetoclax-based regimens for AML patients.
Keyphrases
- acute myeloid leukemia
- endoplasmic reticulum stress
- allogeneic hematopoietic stem cell transplantation
- induced apoptosis
- cell proliferation
- cell cycle arrest
- cancer therapy
- signaling pathway
- oxidative stress
- stem cells
- end stage renal disease
- newly diagnosed
- ejection fraction
- cell death
- dendritic cells
- mesenchymal stem cells
- bone marrow
- small molecule
- drug delivery
- amino acid
- peritoneal dialysis
- single molecule
- chronic kidney disease
- cell therapy
- replacement therapy