Department of Epidemiology and Statistics, School of Public Health, Guilin Medical University, Guilin, 541199, China.
Department of Epidemiology and Statistics, Xiangya School of Public Health, Central South University, Changsha, 410078, China.
BMC Cancer. 2022 Aug 19;22(1):905. doi: 10.1186/s12885-022-09999-y.
Previous study has shown that chemokine-like factor (CKLF)-like MARVEL transmembrane domain-containing family member 4 (CMTM4) can bind and maintain programmed cell death ligand 1 (PD-L1) expression to promote tumor progression by alleviating the suppression of tumor-specific T cell activity, suggesting its potential role in tumor immunotherapy. However, the role of CMTM4 in tumor immunity has not been well clarified, especially in hepatocellular carcinoma (HCC).
The protein expression of CMTM4/PD-L1/CD4/CD8 was detected by immunohistochemistry (IHC) detection in 90 cases of HCC tissues. The mRNA expression profiles and related prognosis data were obtained from The Cancer Genome Atlas-Liver Hepatocellular Carcinoma (TCGA-LIHC). Two immune therapy cohorts were from Imvigor210 and GSE176307.
Though the single protein expression of CMTM4, PD-L1, CD4 or CD8 in HCC tissues by IHC detection didn't show a significant relationship with the prognosis of HCC patients, we found that high co-expression of CMTM4/PD-L1/CD4 showed a good prognosis of HCC patients. Further Timer 2.0 analysis identified that HCC patients with high expression of CMTM4/PD-L1 and high infiltration of CD4 T cells had a better overall survival than those with low infiltration of CD4 T cells. Moreover, a series of bioinformatics analyses revealed that CMTM4-related genes posed important effects on prognosis and immunity in HCC patients, and CMTM4 had a positive correlation with infiltration of CD4 and CD8 T cells in HCC. At last, we used two immunotherapy cohorts to verify that the combination of CMTM4 with PD-L1 could improve the prognosis of tumor patients underwent immunotherapy.
CMTM4 and PD-L1 co-expression with T cell infiltration shows prognostic significance in HCC, suggesting combined effect from multiple proteins should be considered in HCC treatment.
先前的研究表明,趋化因子样因子(CKLF)样膜域包含家族成员 4(CMTM4)可以结合并维持程序性细胞死亡配体 1(PD-L1)的表达,通过减轻对肿瘤特异性 T 细胞活性的抑制来促进肿瘤进展,提示其在肿瘤免疫治疗中的潜在作用。然而,CMTM4 在肿瘤免疫中的作用尚未得到充分阐明,特别是在肝细胞癌(HCC)中。
通过免疫组织化学(IHC)检测在 90 例 HCC 组织中检测 CMTM4/PD-L1/CD4/CD8 的蛋白表达。从癌症基因组图谱-肝肝细胞癌(TCGA-LIHC)中获得 mRNA 表达谱和相关预后数据。两个免疫治疗队列分别来自 Imvigor210 和 GSE176307。
尽管通过 IHC 检测 HCC 组织中 CMTM4、PD-L1、CD4 或 CD8 的单一蛋白表达与 HCC 患者的预后无显著关系,但我们发现 CMTM4/PD-L1/CD4 高共表达的 HCC 患者具有良好的预后。进一步的 Timer 2.0 分析表明,CMTM4/PD-L1 高表达且 CD4 T 细胞浸润高的 HCC 患者的总生存期优于 CD4 T 细胞浸润低的 HCC 患者。此外,一系列生物信息学分析表明,CMTM4 相关基因对 HCC 患者的预后和免疫具有重要影响,CMTM4 与 HCC 中 CD4 和 CD8 T 细胞的浸润呈正相关。最后,我们使用两个免疫治疗队列来验证 CMTM4 与 PD-L1 的联合使用可以改善接受免疫治疗的肿瘤患者的预后。
CMTM4 与 T 细胞浸润的 PD-L1 共表达在 HCC 中具有预后意义,提示在 HCC 治疗中应考虑多种蛋白的联合作用。