Guo Sa, Xing Nan, Du Qinyun, Luo Bin, Wang Shaohui
State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Front Pharmacol. 2024 Jan 12;14:1325992. doi: 10.3389/fphar.2023.1325992. eCollection 2023.
Hepatocellular carcinoma (HCC) is responsible for approximately 90% of liver malignancies and is the third most common cause of cancer-related mortality worldwide. However, the role of anoikis, a programmed cell death mechanism crucial for maintaining tissue equilibrium, is not yet fully understood in the context of HCC. Our study aimed to investigate the expression of 10 anoikis-related genes (ARGs) in HCC, including BIRC5, SFN, UBE2C, SPP1, E2F1, etc., and their significance in the disease. Through Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses, we discovered that these ARGs are involved in important processes such as tissue homeostasis, ion transport, cell cycle regulation, and viral infection pathways. Furthermore, we found a significant correlation between the prognostic value of five ARGs and immune cell infiltrates. Analysis of clinical datasets revealed a strong association between BIRC5 expression and HCC pathological progression, including pathological stage, T stage, overall survival (OS), and race. By constructing a competing endogenous RNA (ceRNA) network and using molecular docking, we identified ten bioactive compounds from traditional Chinese medicine (TCM) that could potentially modulate BIRC5. Subsequent experiments confirmed the influence of platycodin D, one of the identified compounds, on key elements within the ceRNA network. In conclusion, our study presents a novel framework for an anoikis-centered prognostic model and an immune-involved ceRNA network in HCC, revealing potential regulatory targets. These insights contribute to our understanding of HCC pathology and may lead to improved therapeutic interventions.
肝细胞癌(HCC)约占肝脏恶性肿瘤的90%,是全球癌症相关死亡的第三大常见原因。然而,失巢凋亡(一种对维持组织平衡至关重要的程序性细胞死亡机制)在HCC背景下的作用尚未完全明确。我们的研究旨在调查10个与失巢凋亡相关的基因(ARGs)在HCC中的表达,包括BIRC5、SFN、UBE2C、SPP1、E2F1等,以及它们在该疾病中的意义。通过基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路分析,我们发现这些ARGs参与了组织稳态、离子转运、细胞周期调控和病毒感染通路等重要过程。此外,我们发现5个ARGs的预后价值与免疫细胞浸润之间存在显著相关性。临床数据集分析显示BIRC5表达与HCC病理进展密切相关,包括病理分期、T分期、总生存期(OS)和种族。通过构建竞争性内源性RNA(ceRNA)网络并使用分子对接,我们从中药中鉴定出10种可能调节BIRC5的生物活性化合物。随后的实验证实了所鉴定化合物之一的桔梗皂苷D对ceRNA网络关键元件的影响。总之,我们的研究提出了一个以失巢凋亡为中心的HCC预后模型和一个免疫相关ceRNA网络的新框架,揭示了潜在的调控靶点。这些见解有助于我们理解HCC病理,并可能带来改进的治疗干预措施。