Fang Chengnan, Wang Hui, Lin Zhikun, Liu Xinyu, Dong Liwei, Jiang Tianyi, Tan Yexiong, Ning Zhen, Ye Yaorui, Tan Guang, Xu Guowang
CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Cancers (Basel). 2022 Jan 4;14(1):231. doi: 10.3390/cancers14010231.
Hepatocellular carcinoma (HCC) displays a high degree of metabolic and phenotypic heterogeneity and has dismal prognosis in most patients. Here, a gas chromatography-mass spectrometry (GC-MS)-based nontargeted metabolomics method was applied to analyze the metabolic profiling of 130 pairs of hepatocellular tumor tissues and matched adjacent noncancerous tissues from HCC patients. A total of 81 differential metabolites were identified by paired nonparametric test with false discovery rate correction to compare tumor tissues with adjacent noncancerous tissues. Results demonstrated that the metabolic reprogramming of HCC was mainly characterized by highly active glycolysis, enhanced fatty acid metabolism and inhibited tricarboxylic acid cycle, which satisfied the energy and biomass demands for tumor initiation and progression, meanwhile reducing apoptosis by counteracting oxidative stress. Risk stratification was performed based on the differential metabolites between tumor and adjacent noncancerous tissues by using nonnegative matrix factorization clustering. Three metabolic clusters displaying different characteristics were identified, and the cluster with higher levels of free fatty acids (FFAs) in tumors showed a worse prognosis. Finally, a metabolite classifier composed of six FFAs was further verified in a dependent sample set to have potential to define the patients with poor prognosis. Together, our results offered insights into the molecular pathological characteristics of HCC.
肝细胞癌(HCC)表现出高度的代谢和表型异质性,大多数患者预后不佳。在此,应用基于气相色谱 - 质谱联用(GC-MS)的非靶向代谢组学方法,分析了130对来自HCC患者的肝细胞肿瘤组织及其配对的癌旁非肿瘤组织的代谢谱。通过配对非参数检验并进行错误发现率校正,比较肿瘤组织与癌旁非肿瘤组织,共鉴定出81种差异代谢物。结果表明,HCC的代谢重编程主要表现为糖酵解高度活跃、脂肪酸代谢增强以及三羧酸循环受抑制,这满足了肿瘤起始和进展所需的能量和生物量需求,同时通过对抗氧化应激减少细胞凋亡。利用非负矩阵分解聚类法,基于肿瘤组织与癌旁非肿瘤组织之间的差异代谢物进行风险分层。识别出三个具有不同特征的代谢簇,肿瘤中游离脂肪酸(FFA)水平较高簇的预后较差。最后,在一个独立样本集中进一步验证了由六种FFA组成的代谢物分类器,其具有定义预后不良患者的潜力。总之,我们的结果为HCC的分子病理特征提供了见解。