Yu Jiahao, Ma Shuoyi, Tian Siyuan, Zhang Miao, Ding Xiaopeng, Liu Yansheng, Yang Fangfang, Hu Yinan, Xuan Guoyun, Zhou Xinmin, Wang Jingbo, Han Ying
State Key Laboratory of Cancer Biology, Xijing Hospital of Digestive Diseases, The Fourth Military Medical University, Xi'an, China.
Front Cell Dev Biol. 2021 Oct 4;9:700553. doi: 10.3389/fcell.2021.700553. eCollection 2021.
Hepatocellular carcinoma (HCC), a highly aggressive tumor, has high incidence and mortality rates. Recently, immunotherapies have been shown to be a promising treatment in HCC. The results of either the CheckMate-040 or IMbrave 150 trials demonstrate the importance of immunotherapy in the systemic treatment of liver cancer. Thus, in this study, we tried to establish a reliable prognostic model for liver cancer based on immune-related genes (IRGs) and to provide a new insight for immunotherapy of HCC. In this study, we used four datasets that incorporated 851 HCC samples, including 340 samples with complete clinical information from the cancer genome atlas (TCGA) database, to establish an effective model for predicting the prognosis of HCC patients based on the differential expression of IRGs and validated the prognostic model using the data from International Cancer Genome Consortium (ICGC). The top 6 characteristic IRGs identified by protein-protein interaction (PPI) network analysis, MMP9, FOS, CAT, ESR1, ANGPTL3, and KLKB1, were selected for further study. In addition, we assessed the correlations of the six characteristic IRGs with the tumor immune microenvironment, clinical stage, and sensitivity to anti-cancer drugs. We also explored whether the differential expression of the characteristic IRGs was specific to HCC or present in pan-cancer. The expression levels of the six characteristic IRGs were significantly different between most tumor tissues and adjacent normal tissues. In addition, these characteristic IRGs showed a strong association with immune cell infiltration in HCC patients. We found that MMP9 and ESR1 were independent prognostic factors for HCC, while CAT, ESR1, and KLKB1 were associated with the clinical stage. We collected HCC paraffin sections from 24 patients from Xijing hospital to identify the differential expression of the five genes (MMP9, ESR1, CAT, FOS, and KLKB1). Finally, the results of decision curve analysis (DCA) and nomogram revealed that our models provided a prognostic benefit for most HCC patients and the predicted overall survival (OS) was consistent with the actual OS. In conclusion, we systemically constructed a novel prognostic model that provides new insights into HCC.
肝细胞癌(HCC)是一种侵袭性很强的肿瘤,发病率和死亡率都很高。最近,免疫疗法已被证明是HCC一种很有前景的治疗方法。CheckMate-040或IMbrave 150试验的结果证明了免疫疗法在肝癌全身治疗中的重要性。因此,在本研究中,我们试图基于免疫相关基因(IRG)建立一种可靠的肝癌预后模型,并为HCC的免疫治疗提供新的见解。在本研究中,我们使用了四个包含851个HCC样本的数据集,其中包括来自癌症基因组图谱(TCGA)数据库的340个具有完整临床信息的样本,以基于IRG的差异表达建立一个预测HCC患者预后的有效模型,并使用国际癌症基因组联盟(ICGC)的数据验证了该预后模型。通过蛋白质-蛋白质相互作用(PPI)网络分析确定的前6个特征性IRG,即基质金属蛋白酶9(MMP9)、原癌基因c-Fos(FOS)、过氧化氢酶(CAT)、雌激素受体1(ESR1)、血管生成素样蛋白3(ANGPTL3)和激肽释放酶B1(KLKB1),被选作进一步研究。此外,我们评估了这6个特征性IRG与肿瘤免疫微环境、临床分期以及对抗癌药物敏感性的相关性。我们还探讨了特征性IRG的差异表达是否是HCC特有的,还是存在于泛癌中。大多数肿瘤组织与癌旁正常组织之间,这6个特征性IRG的表达水平存在显著差异。此外,这些特征性IRG与HCC患者的免疫细胞浸润密切相关。我们发现MMP9和ESR1是HCC的独立预后因素,而CAT、ESR1和KLKB1与临床分期有关。我们收集了西京医院24例患者的HCC石蜡切片,以鉴定5个基因(MMP9、ESR1、CAT、FOS和KLKB1)的差异表达。最后,决策曲线分析(DCA)和列线图的结果显示,我们的模型为大多数HCC患者提供了预后益处,预测的总生存期(OS)与实际OS一致。总之,我们系统地构建了一种新的预后模型,为HCC提供了新的见解。