Li Jie, Xu Siyi, Zhu Feng, Shen Fei, Zhang Tianyi, Wan Xin, Gong Saisai, Liang Geyu, Zhou Yonglin
Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, 210009, Jiangsu, China.
Jiangsu Provincial Key Laboratory of Critical Care Medicine, School of Public Health, Southeast University, Nanjing, 210009, China.
Curr Med Chem. 2024;31(40):6692-6712. doi: 10.2174/0109298673284520240112055108.
Gastric cancer (GC) is a highly intricate gastrointestinal malignancy. Early detection of gastric cancer forms the cornerstone of precision medicine. Several studies have been conducted to investigate early biomarkers of gastric cancer using genomics, transcriptomics, proteomics, and metabolomics, respectively. However, endogenous substances associated with various omics are concurrently altered during gastric cancer development. Furthermore, environmental exposures and family history can also induce modifications in endogenous substances. Therefore, in this study, we primarily investigated alterations in DNA mutation, DNA methylation, mRNA, lncRNA, miRNA, circRNA, and protein, as well as glucose, amino acid, nucleotide, and lipid metabolism levels in the context of GC development, employing genomics, transcriptomics, proteomics, and metabolomics. Additionally, we elucidate the impact of exposure factors, including HP, EBV, nitrosamines, smoking, alcohol consumption, and family history, on diagnostic biomarkers of gastric cancer. Lastly, we provide a summary of the application of machine learning in integrating multi-omics data. Thus, this review aims to elucidate: i) the biomarkers of gastric cancer related to genomics, transcriptomics, proteomics, and metabolomics; ii) the influence of environmental exposure and family history on multiomics data; iii) the integrated analysis of multi-omics data using machine learning techniques.
胃癌(GC)是一种高度复杂的胃肠道恶性肿瘤。早期发现胃癌是精准医学的基石。分别利用基因组学、转录组学、蛋白质组学和代谢组学开展了多项研究来探究胃癌的早期生物标志物。然而,在胃癌发生发展过程中,与各种组学相关的内源性物质会同时发生改变。此外,环境暴露和家族史也会诱导内源性物质发生改变。因此,在本研究中,我们主要利用基因组学、转录组学、蛋白质组学和代谢组学,研究了胃癌发生发展过程中DNA突变、DNA甲基化、mRNA、lncRNA、miRNA、circRNA和蛋白质的变化,以及葡萄糖、氨基酸、核苷酸和脂质代谢水平。此外,我们阐明了幽门螺杆菌(HP)、EB病毒(EBV)、亚硝胺、吸烟、饮酒和家族史等暴露因素对胃癌诊断生物标志物的影响。最后,我们总结了机器学习在整合多组学数据中的应用。因此,本综述旨在阐明:i)与基因组学、转录组学、蛋白质组学和代谢组学相关的胃癌生物标志物;ii)环境暴露和家族史对多组学数据的影响;iii)使用机器学习技术对多组学数据进行综合分析。