Department of Medical Research, E-Da Hospital, I-Shou University, Kaohsiung 824410, Taiwan; Graduate Institute of Medicine, I-Shou University, Kaohsiung 824410, Taiwan.
Departmentof Nursing, Fooyin University, Kaohsiung 831301, Taiwan.
J Adv Res. 2024 Aug;62:229-243. doi: 10.1016/j.jare.2024.03.019. Epub 2024 Mar 27.
Overwhelming neutrophil activation and oxidative stress significantly contribute to acute respiratory distress syndrome (ARDS) pathogenesis. However, the potential of repurposing ribociclib, a cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor used clinically in cancer treatment, for treating neutrophilic ARDS remains uncertain. This study illustrated the ability and underlying mechanism of ribociclib for treating ARDS and neutrophilic inflammation.
Primary human neutrophils were used to determine the therapeutic effects of ribociclib on respiratory bursts, chemotactic responses, and inflammatory signaling. In vitro and silico analyses were performed to determine the underlying molecular mechanisms. The potential of ribociclib repurposing was evaluated using an in vivo ARDS model in lipopolysaccharide (LPS)-primed mice.
We found that treatment using ribociclib markedly limited overabundant oxidative stress (reactive oxygen species [ROS]) production and chemotactic responses (integrin levels and adhesion) in activated human neutrophils. Ribociclib was also shown to act as a selective inhibitor of phosphodiesterase 4 (PDE4), thereby promoting the cyclic adenosine monophosphate (cAMP)-protein kinase A (PKA) pathway, leading to the inhibition of extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK) phosphorylation, and calcium influx. Notably, prophylactic administration and post-treatment with ribociclib ameliorated neutrophil infiltration, lung inflammation, accumulation of oxidative stress, pulmonary destruction, and mortality in mice with LPS-induced ARDS.
We demonstrated for the first time that ribociclib serves as a novel PDE4 inhibitor for treating neutrophilic inflammation and ARDS. The repurposing ribociclib and targeting neutrophilic PDE4 offer a potential off-label alternative for treating lung lesions and other inflammatory conditions.
过度的中性粒细胞激活和氧化应激对急性呼吸窘迫综合征(ARDS)的发病机制有重要影响。然而,将临床用于癌症治疗的细胞周期蛋白依赖性激酶 4 和 6(CDK4/6)抑制剂来那度胺(ribociclib)重新用于治疗中性粒细胞性 ARDS 的潜力尚不确定。本研究阐明了来那度胺治疗 ARDS 和中性粒细胞炎症的能力及其潜在机制。
使用原代人中性粒细胞来确定来那度胺对呼吸爆发、趋化反应和炎症信号的治疗作用。进行体外和计算机分析以确定潜在的分子机制。使用脂多糖(LPS)预刺激的小鼠 ARDS 模型评估来那度胺的重新利用潜力。
我们发现,来那度胺治疗可显著限制激活的人中性粒细胞中过多的氧化应激(活性氧[ROS])产生和趋化反应(整合素水平和黏附)。来那度胺还被证明是磷酸二酯酶 4(PDE4)的选择性抑制剂,从而促进环磷酸腺苷(cAMP)-蛋白激酶 A(PKA)途径,导致细胞外信号调节激酶(ERK)、c-Jun N 端激酶(JNK)磷酸化和钙内流的抑制。值得注意的是,预防性给予和后期给予来那度胺可改善 LPS 诱导的 ARDS 小鼠中性粒细胞浸润、肺炎症、氧化应激积累、肺破坏和死亡率。
我们首次证明来那度胺可作为治疗中性粒细胞炎症和 ARDS 的新型 PDE4 抑制剂。来那度胺的重新利用和靶向中性粒细胞 PDE4 为治疗肺部病变和其他炎症性疾病提供了一种潜在的非标签替代方案。