探讨鼻咽癌中脂质代谢相关基因生物标志物及其调控机制。

IF 2.2 4区 医学 Q3 ONCOLOGY
Cancer Biomarkers Pub Date : 2025-04-01 Epub Date: 2025-04-28 DOI:10.1177/18758592241301683
Yiyi Liu, Yingying Xie, Yong Wang
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引用次数: 0

摘要

背景:鼻咽癌(NPC)是一种起源于鼻咽粘膜的肿瘤。最近的研究强调,脂质代谢重编程是肿瘤细胞中一个显著的代谢改变。因此,鉴定鼻咽癌中脂质代谢相关的生物标志物至关重要。方法利用转录组学数据,从鼻咽癌GSE12452中鉴定差异表达基因(DEGs),并与正常对照进行比较。采用加权基因共表达网络分析(Weighted Gene Co-expression Network Analysis, WGCNA)识别NPC相关的关键模块基因。脂质代谢相关差异表达基因(LMR-DEGs)通过交叉DEGs、与NPC相关的关键模块基因和脂质代谢相关基因(LMRGs)使用维恩图方法确定。随后,MCODE算法在蛋白-蛋白相互作用(PPI)框架内应用,以确定鼻咽癌以脂质代谢为中心的生物标志物。通过ROC分析评估这些生物标志物的诊断潜力。在最后阶段,使用Cytoscape描绘了一个“TF-mRNA-miRNA”相互作用网络。结果在我们的分析中,当将NPC标本与正常对照进行比较时,共识别出5026个deg。从这个基因池中,确定了1835个基因是与NPC相关的关键模块基因。通过维恩图方法分离64个lmr - deg。进一步分析鉴定出6个以脂质代谢为中心的NPC生物标志物,即GALC、SPTLC2、SMPD2、DEGS2、DEGS1和SMPD3。值得注意的是,这些生物标志物显示出强大的诊断功效。我们发现DEGS1与SMPD2和DEGS2呈负相关。一项比较表达分析显示,与对照组相比,NPC队列中GALC、SPTLC2、SMPD2、DEGS2和SMPD3的表达水平降低。在研究的最后阶段,我们描绘了由309个节点和360个相互作用对组成的“TF-mRNA-miRNA”调控网络。总之,我们的研究确定了与鼻咽癌相关的6种脂质代谢相关生物标志物(GALC、SPTLC2、SMPD2、DEGS2、DEGS1和SMPD3),为潜在的鼻咽癌治疗干预提供了基础框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring lipid metabolism-associated gene biomarkers and their regulatory mechanisms in nasopharyngeal carcinoma.

BackgroundNasopharyngeal carcinoma (NPC) is a neoplasm that arises from the mucosal lining of the nasopharynx. Recent investigations have underscored that reprogramming of lipid metabolism is a salient metabolic alteration in neoplastic cells. Consequently, identifying lipid metabolism-associated biomarkers in NPC is of paramount importance.MethodsUtilizing transcriptomic datasets, differentially expressed genes (DEGs) were identified from GSE12452, contrasting NPC specimens with normal controls. The Weighted Gene Co-expression Network Analysis (WGCNA) was employed to discern key module genes pertinent to NPC. Lipid metabolism-related differentially expressed genes (LMR-DEGs) were ascertained by intersecting DEGs, key module genes linked to NPC, and lipid metabolism-related genes (LMRGs) using a Venn diagram approach. Subsequently, the MCODE algorithm was applied within the protein-protein interaction (PPI) framework to pinpoint lipid metabolism-centric biomarkers for NPC. The diagnostic potential of these biomarkers was assessed through ROC analysis. In the concluding phase, a 'TF-mRNA-miRNA' interaction network was delineated using Cytoscape.ResultsIn our analysis, a total of 5026 DEGs were discerned when contrasting NPC specimens with normal controls. From this pool, 1835 genes were pinpointed as key module genes pertinent to NPC. Through a Venn diagram approach, 64 LMR-DEGs were isolated. Further analysis led to the identification of six lipid metabolism-centric biomarkers for NPC, namely GALC, SPTLC2, SMPD2, DEGS2, DEGS1, and SMPD3. Notably, these biomarkers demonstrated robust diagnostic efficacy. We found that DEGS1 was negatively correlated with SMPD2 and DEGS2. A comparative expression analysis revealed diminished expression levels of GALC, SPTLC2, SMPD2, DEGS2, and SMPD3 in the NPC cohort relative to the control group. In the terminal phase of our study, the 'TF-mRNA-miRNA' regulatory network was delineated, comprising 309 nodes and 360 interaction pairs.ConclusionIn summary, our investigation identified six lipid metabolism-associated biomarkers (GALC, SPTLC2, SMPD2, DEGS2, DEGS1, and SMPD3) linked to NPC, providing a foundational framework for potential therapeutic interventions for NPC.

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来源期刊
Cancer Biomarkers
Cancer Biomarkers ONCOLOGY-
CiteScore
5.20
自引率
3.20%
发文量
195
审稿时长
3 months
期刊介绍: Concentrating on molecular biomarkers in cancer research, Cancer Biomarkers publishes original research findings (and reviews solicited by the editor) on the subject of the identification of markers associated with the disease processes whether or not they are an integral part of the pathological lesion. The disease markers may include, but are not limited to, genomic, epigenomic, proteomics, cellular and morphologic, and genetic factors predisposing to the disease or indicating the occurrence of the disease. Manuscripts on these factors or biomarkers, either in altered forms, abnormal concentrations or with abnormal tissue distribution leading to disease causation will be accepted.
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