Xiong Wei, Deng Ying
Department of Hepatobiliary Surgery, Sichuan Provincial People's Hospital, Chengdu, CHN.
Cancer Center, Sichuan Provincial People's Hospital, Chengdu, CHN.
Cureus. 2024 Jun 13;16(6):e62287. doi: 10.7759/cureus.62287. eCollection 2024 Jun.
The basigin (BSG) gene, also known as CD147, has been implicated in the progression and prognosis of various cancers, including liver cancer. This study aimed to comprehensively evaluate the prognostic value of total BSG expression and its specific transcript variants, ENST00000353555 and ENST00000545507, in a large cohort of patients with primary liver cancer.
The prognostic values of total BSG, ENST00000353555, and ENST00000545507 expression in overall survival (OS) and progression-free interval (PFI) of patients with primary liver cancer were assessed using The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) dataset. Survival analysis, receiver operating characteristic (ROC) analysis, and validation of an extracellular matrix (ECM)-related prognostic signature were performed.
In univariate and multivariate analyses, total BSG, ENST00000353555, and ENST00000545507 expression were associated with poor OS in liver cancer patients. ENST00000353555 showed the highest hazard ratio among the three prognostic indicators. ROC analysis revealed that ENST00000353555 had better prognostic performance than total BSG expression. Replacing total BSG with ENST00000353555 in an existing ECM-related prognostic signature marginally increased the area under the curve values for one year from 0.79 to 0.80, and five-year OS from 0.72 to 0.73. ENST00000353555 showed isoform-specific positive correlations with EDNRB, IL10, C10orf54, and VEGFA.
ENST00000353555 serves as a better prognostic biomarker than total BSG expression in liver cancer, either as an individual marker or as a component of an ECM-related gene signature. Additionally, ENST00000353555 exhibited isoform-specific positive correlations with several immunosuppressive genes, suggesting a potential role in regulating the tumor microenvironment.
基底膜聚糖(BSG)基因,也称为CD147,已被证明与包括肝癌在内的多种癌症的进展和预后有关。本研究旨在全面评估原发性肝癌患者大样本队列中总BSG表达及其特定转录变体ENST00000353555和ENST00000545507的预后价值。
使用癌症基因组图谱肝细胞癌(TCGA-LIHC)数据集评估原发性肝癌患者总BSG、ENST00000353555和ENST00000545507表达在总生存期(OS)和无进展生存期(PFI)中的预后价值。进行了生存分析、受试者工作特征(ROC)分析以及细胞外基质(ECM)相关预后特征的验证。
在单变量和多变量分析中,总BSG、ENST00000353555和ENST00000545507表达与肝癌患者的不良OS相关。在三个预后指标中,ENST00000353555的风险比最高。ROC分析显示,ENST00000353555的预后性能优于总BSG表达。在现有的ECM相关预后特征中,用ENST00000353555替代总BSG,曲线下面积值在1年时从0.79略微增加到0.80,5年OS从0.72增加到0.73。ENST00000353555与EDNRB、IL10、C10orf54和VEGFA表现出亚型特异性正相关。
无论是作为个体标志物还是作为ECM相关基因特征的组成部分,ENST00000353555在肝癌中都是比总BSG表达更好的预后生物标志物。此外,ENST00000353555与几种免疫抑制基因表现出亚型特异性正相关,表明其在调节肿瘤微环境中可能发挥作用。