Chen Wenbiao, Zhang Feng, Xu Huixuan, Hou Xianliang, Tang Donge
Central Molecular Laboratory, People's Hospital of Longhua, The Affiliated Hospital of Southern Medical University, Shenzhen, 518109, China.
Department of Respiratory Medicine, People's Hospital of Longhua, The Affiliated Hospital of Southern Medical University, Shenzhen, 518109, China.
Curr Genomics. 2022 Jun 10;23(2):109-117. doi: 10.2174/1389202923666220304125458.
Extracellular vehicles (EVs) contain different proteins that relay information between tumor cells, thus promoting tumorigenesis. Therefore, EVs can serve as an ideal marker for tumor pathogenesis and clinical application. Here, we characterised EV-specific proteins in hepatocellular carcinoma (HCC) samples and established their potential protein-protein interaction (PPI) networks. We used multi-dimensional bioinformatics methods to mine a network module to use as a prognostic signature and validated the model's prediction using additional datasets. The relationship between the prognostic model and tumor immune cells or the tumor microenvironment status was also examined. 1134 proteins from 316 HCC samples were mapped to the exoRBase database. HCC-specific EVs specifically expressed a total of 437 proteins. The PPI network revealed 321 proteins and 938 interaction pathways, which were mined to identify a three network module (3NM) with significant prognostic prediction ability. Validation of the 3NM in two more datasets demonstrated that the model outperformed the other signatures in prognostic prediction ability. Functional analysis revealed that the network proteins were involved in various tumor-related pathways. Additionally, these findings demonstrated a favorable association between the 3NM signature and macrophages, dendritic, and mast cells. Besides, the 3NM revealed the tumor microenvironment status, including hypoxia and inflammation. These findings demonstrate that the 3NM signature reliably predicts HCC pathogenesis. Therefore, the model may be used as an effective prognostic biomarker in managing patients with HCC.
细胞外囊泡(EVs)包含不同的蛋白质,这些蛋白质在肿瘤细胞之间传递信息,从而促进肿瘤发生。因此,EVs可作为肿瘤发病机制和临床应用的理想标志物。在此,我们对肝细胞癌(HCC)样本中的EV特异性蛋白质进行了表征,并建立了它们潜在的蛋白质-蛋白质相互作用(PPI)网络。我们使用多维生物信息学方法挖掘一个网络模块作为预后特征,并使用其他数据集验证了该模型的预测。还研究了预后模型与肿瘤免疫细胞或肿瘤微环境状态之间的关系。来自316个HCC样本的1134种蛋白质被映射到exoRBase数据库。HCC特异性EVs共特异性表达437种蛋白质。PPI网络揭示了321种蛋白质和938条相互作用途径,通过挖掘这些信息确定了一个具有显著预后预测能力的三网络模块(3NM)。在另外两个数据集中对3NM进行验证表明,该模型在预后预测能力方面优于其他特征。功能分析表明,网络蛋白参与了各种肿瘤相关途径。此外,这些发现表明3NM特征与巨噬细胞、树突状细胞和肥大细胞之间存在良好的关联。此外,3NM揭示了肿瘤微环境状态,包括缺氧和炎症。这些发现表明3NM特征能够可靠地预测HCC发病机制。因此,该模型可作为管理HCC患者的有效预后生物标志物。