Integrative multiomics analysis identifies molecular subtypes and potential targets of hepatocellular carcinoma

肝细胞癌 生物标志物发现 计算生物学 代谢组学 生物 代谢组 无线电技术 病理 医学 癌症研究 生物信息学 蛋白质组学 遗传学 放射科 基因
作者
Shuai Yang,Lu Zheng,Lingling Li,Jiangang Zhang,Jingchun Wang,Huakan Zhao,Yu Chen,Xudong Liu,Hui Kong Gan,Junying Chen,Mei Yan,Chuanyin He,Kai Li,Chen Ding,Yongsheng Li
出处
期刊:Clinical and translational medicine [Springer Science+Business Media]
卷期号:14 (6): e1727-e1727 被引量:16
标识
DOI:10.1002/ctm2.1727
摘要

BACKGROUND: The liver is anatomically divided into eight segments based on the distribution of Glisson's triad. However, the molecular mechanisms underlying each segment and its association with hepatocellular carcinoma (HCC) heterogeneity are not well understood. In this study, our objective is to conduct a comprehensive multiomics profiling of the segmentation atlas in order to investigate potential subtypes and therapeutic approaches for HCC. METHODS: A high throughput liquid chromatography-tandem mass spectrometer strategy was employed to comprehensively analyse proteome, lipidome and metabolome data, with a focus on segment-resolved multiomics profiling. To classify HCC subtypes, the obtained data with normal reference profiling were integrated. Additionally, potential therapeutic targets for HCC were identified using immunohistochemistry assays. The effectiveness of these targets were further validated through patient-derived organoid (PDO) assays. RESULTS: A multiomics profiling of 8536 high-confidence proteins, 1029 polar metabolites and 3381 nonredundant lipids was performed to analyse the segmentation atlas of HCC. The analysis of the data revealed that in normal adjacent tissues, the left lobe was primarily involved in energy metabolism, while the right lobe was associated with small molecule metabolism. Based on the normal reference atlas, HCC patients with segment-resolved classification were divided into three subtypes. The C1 subtype showed enrichment in ribosome biogenesis, the C2 subtype exhibited an intermediate phenotype, while the C3 subtype was closely associated with neutrophil degranulation. Furthermore, using the PDO assay, exportin 1 (XPO1) and 5-lipoxygenase (ALOX5) were identified as potential targets for the C1 and C3 subtypes, respectively. CONCLUSION: Our extensive analysis of the segmentation atlas in multiomics profiling defines molecular subtypes of HCC and uncovers potential therapeutic strategies that have the potential to enhance the prognosis of HCC.
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