Synergistic effects of arsenic trioxide and atorvastatin on proliferation and apoptosis in acute lymphoblastic leukemia cells

IF 0.8 Q4 HEMATOLOGY
Leukemia Research Reports Pub Date : 2026-01-01 Epub Date: 2026-02-16 DOI:10.1016/j.lrr.2026.100570
Sepideh Hassanpour Khodaei , Shahnaz Sabetkam , Zeinab Mazloumi , Ali Rafat , Diana Hekari , Khadijeh Dizaji Asl
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引用次数: 0

Abstract

Statins and arsenic trioxide (ATO) are known for their significant anti-neoplastic properties; however, limited research has investigated their potential synergistic effects. This study explores the individual and combined impact of ATO and atorvastatin on programmed cell death and proliferation in acute lymphoblastic leukemia (ALL) cell model. The ALL cell line was exposed to different doses of atorvastatin and ATO, both individually and in combination, to evaluate their respective IC50 values and identify the most effective concentrations. The proportions of apoptotic cells were quantified using Annexin V/PI staining, while Ki-67 expression, a well-established marker of cell proliferation, was assessed through flow cytometry. The findings revealed that atorvastatin and ATO, at concentrations of 12.4 µM and 3.34 µM, respectively, significantly enhanced apoptosis in ALL cells. Moreover, the combination therapy resulted in a marked increase in anti-proliferative effects. These findings provide new insights into the potential use of ATO and atorvastatin as a combined therapeutic strategy, highlighting their promise as a novel approach in the treatment of ALL.
三氧化二砷和阿托伐他汀对急性淋巴细胞白血病细胞增殖和凋亡的协同作用
他汀类药物和三氧化二砷(ATO)以其显著的抗肿瘤特性而闻名;然而,有限的研究调查了它们潜在的协同效应。本研究探讨ATO和阿托伐他汀对急性淋巴细胞白血病(ALL)细胞模型的程序性细胞死亡和增殖的单独和联合影响。将ALL细胞系单独或联合暴露于不同剂量的阿托伐他汀和ATO,以评估其各自的IC50值并确定最有效的浓度。Annexin V/PI染色定量凋亡细胞比例,流式细胞术检测细胞增殖标志物Ki-67的表达。结果显示,阿托伐他汀和ATO浓度分别为12.4µM和3.34µM时,可显著促进ALL细胞的凋亡。此外,联合治疗导致抗增殖作用显著增加。这些发现为ATO和阿托伐他汀作为联合治疗策略的潜在应用提供了新的见解,突出了它们作为治疗ALL的新方法的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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