Song Congkuan, Li Qingqing, Zhang Jinjin, Hu Weidong
Department of Thoracic Surgery, Zhongnan Hospital of Wuhan University, No.169 Donghu Road, Wuchang District, Wuhan, 430071, China.
Hubei Provincial Clinical Research Center for Cancer, No.169 Donghu Road, Wuchang District, Wuhan, 430071, China.
Inflammation. 2025 Feb 19. doi: 10.1007/s10753-025-02270-z.
The specific pathogenesis of acute lung injury (ALI) is complex and not yet clear, and the clinical treatment methods are relatively limited. It is of great clinical significance to explore its pathogenesis and effective molecular targets. Here, we identified an ALI biomarker (UPP1) associated with uridine metabolism by a systematic bioinformatics approach. It was also confirmed to be associated with the glycolytic pathway in the mouse ALI model. In addition, drug sensitivity analysis based on the CMAP database identified three UPP1-associated drugs (CAY10585, XL147 and IOX2) that may be useful in the treatment of ALI. Molecular docking and molecular dynamics simulations further confirmed the stability of the binding between UPP1 and the three drugs. In conclusion, this study confirms that the uridine metabolism gene UPP1 associated with glycolysis is a key biomarker of ALI and provides valuable insights into the potential application of CAY10585, XL147 and IOX2 in ALI.
急性肺损伤(ALI)的具体发病机制复杂且尚不清楚,临床治疗方法相对有限。探索其发病机制和有效的分子靶点具有重要的临床意义。在此,我们通过系统的生物信息学方法鉴定了一种与尿苷代谢相关的ALI生物标志物(UPP1)。在小鼠ALI模型中,它也被证实与糖酵解途径相关。此外,基于CMAP数据库的药物敏感性分析确定了三种可能对ALI治疗有用的UPP1相关药物(CAY10585、XL147和IOX2)。分子对接和分子动力学模拟进一步证实了UPP1与这三种药物结合的稳定性。总之,本研究证实与糖酵解相关的尿苷代谢基因UPP1是ALI的关键生物标志物,并为CAY10585、XL147和IOX2在ALI中的潜在应用提供了有价值的见解。