Ketzer Franz, Büttner Ulrike, Geist Daniel, Kick Anita, Wirth Thomas, Ushmorov Alexey
Institute of Clinical Chemistry and Pathobiochemistry, TUM School of Medicine and Health, Technical University of Munich, Munich, Germany.
Institute of Physiological Chemistry, University of Ulm, Ulm, Germany.
Blood Adv. 2025 Jul 22;9(14):3441-3454. doi: 10.1182/bloodadvances.2024015560.
Activation of the transcription factor forkhead box O1 (FOXO1) contributes to multiple pathological processes. The FOXO1 inhibitor AS1842856 demonstrated strong therapeutic effects in preclinical models of common diseases such as diabetes and anthracycline-induced heart failure. We have previously identified FOXO1 as a B-cell acute lymphoblastic leukemia (B-ALL) dependency and demonstrated in in vivo B-ALL models that AS1842856 increased the survival of animals and decreased B-ALL tumor load in all critical organ compartments, but most efficiently in the central nervous system. Here, we interrogated the underlying molecular mechanisms by comparison of the transcriptomic effects of AS1842856 and Foxo1 knockout (Foxo1-KO) in a B-ALL mouse model. Despite the significant similarity in sets of regulated genes, we identified glycogen synthase kinase (GSK) 3B inhibition as a signature enriched only in AS1842856-treated cells. Using an in vitro kinase assay and an unbiased kinome screen, we identified AS1842856 as a direct GSK3 inhibitor that ultimately stabilizes CTNNB1. CTNNB1-KO partially protected B-ALL cell lines from the cytotoxic effect of AS1842856. At the same time, using a chemical protein degradation model, we found that FOXO1 indeed contributes to the cytotoxic effect of AS1842856. We conclude that AS1842856 targets 2 B-lymphoid vulnerabilities: GSK3 and FOXO1. The unique mode of action, low toxicity, and ability to penetrate the blood-brain barrier warrant further investigation of the therapeutic potential of AS1842856 in B-ALL.
转录因子叉头框O1(FOXO1)的激活参与多种病理过程。FOXO1抑制剂AS1842856在糖尿病和蒽环类药物诱导的心力衰竭等常见疾病的临床前模型中显示出强大的治疗效果。我们之前已确定FOXO1是B细胞急性淋巴细胞白血病(B-ALL)的一个依赖因素,并在体内B-ALL模型中证明,AS1842856可提高动物存活率,并降低所有关键器官腔室中的B-ALL肿瘤负荷,在中枢神经系统中效果最为显著。在此,我们通过比较AS1842856和Foxo1基因敲除(Foxo1-KO)在B-ALL小鼠模型中的转录组效应,探究其潜在分子机制。尽管调控基因集有显著相似性,但我们发现糖原合酶激酶(GSK)3B抑制是仅在AS1842856处理细胞中富集的一个特征。通过体外激酶测定和无偏向性激酶组筛选,我们确定AS1842856是一种直接的GSK3抑制剂,最终可稳定CTNNB1。CTNNB1基因敲除可部分保护B-ALL细胞系免受AS1842856的细胞毒性作用。同时,利用化学蛋白质降解模型,我们发现FOXO1确实对AS1842856的细胞毒性作用有影响。我们得出结论,AS1842856靶向2个B淋巴细胞易损因素:GSK3和FOXO1。其独特的作用方式、低毒性以及穿透血脑屏障的能力,值得进一步研究AS1842856在B-ALL中的治疗潜力。