Park Ki-Hoon, Kim Seok-Hyung, Kim So-Woon, Na Kiyong, Kim Sunyoung, Choi Young-Il, Chung Hyung-Joo, Jung Junyang, Jeong Na Young
Department of Anesthesiology and Pain Medicine, College of Medicine, Kosin University, South Korea.
Department of Anatomy and Neurobiology, College of Medicine, Kyung Hee University, South Korea.
Clin Exp Hepatol. 2025 Mar;11(1):71-80. doi: 10.5114/ceh.2025.146956. Epub 2025 Mar 7.
We investigated whether nicotinamide adenine dinucleotide kinase (NADK) expression is selectively diminished in alcohol-associated liver cirrhosis (AC), and evaluated its potential as a biomarker for this condition.
Human liver samples were obtained during liver transplantation or resection procedures at Kosin University Gospel Hospital and classified into two groups: AC and non-AC (NAC). NAD and NADP levels were measured using liquid chromatography-mass spectrometry (LC-MS). RNA-seq data from the NCBI Gene Expression Omnibus were utilized to identify AC-specific differentially expressed genes (DEGs). Multi-level expression analyses and immunohistochemistry were performed to assess NADK expression in liver tissues.
LC-MS analysis indicated a significant reduction in NAD and NADP levels in AC patients compared to both normal and NAC groups, with a corresponding increase in the NAD/NADP ratio (AC = 3.93, NAC = 2.75, normal = 2.64). We identified 881 AC-specific DEGs, including 27 kinase-encoding genes. Multi-level expression analyses confirmed a significant decrease in NADK gene expression in AC patients. Immunohistochemistry showed a marked reduction in NADK protein expression in AC patients, underscoring its involvement in altered metabolic processes.
This study revealed a distinct decrease in NADK expression in AC, suggesting its utility as a molecular marker for diagnosing and understanding metabolic dysregulation in these patients. These findings provide a foundation for developing targeted therapeutic strategies for alcohol-associated liver cirrhosis.
我们调查了烟酰胺腺嘌呤二核苷酸激酶(NADK)在酒精性肝硬化(AC)中表达是否选择性降低,并评估其作为该疾病生物标志物的潜力。
在釜庆大学福音医院的肝移植或切除手术过程中获取人类肝脏样本,并分为两组:AC组和非AC组(NAC组)。使用液相色谱 - 质谱联用(LC-MS)测量NAD和NADP水平。利用来自NCBI基因表达综合数据库的RNA-seq数据鉴定AC特异性差异表达基因(DEG)。进行多层次表达分析和免疫组织化学以评估肝脏组织中NADK的表达。
LC-MS分析表明,与正常组和NAC组相比,AC患者的NAD和NADP水平显著降低,NAD/NADP比值相应增加(AC = 3.93,NAC = 2.75,正常 = 2.64)。我们鉴定出881个AC特异性DEG,包括27个编码激酶的基因。多层次表达分析证实AC患者中NADK基因表达显著降低。免疫组织化学显示AC患者中NADK蛋白表达明显减少,强调其参与了代谢过程的改变。
本研究揭示了AC中NADK表达明显降低,表明其作为诊断和理解这些患者代谢失调的分子标志物的效用。这些发现为开发酒精性肝硬化的靶向治疗策略提供了基础。