Li Yao Jun, Li Hai Yan, Zhang Quan, Wei Sheng Li
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Tianjin Huanhu Hospital, Tianjin, China.
Front Genet. 2022 Jul 22;13:942785. doi: 10.3389/fgene.2022.942785. eCollection 2022.
Cuproptosis has been recognized as a novel regulatory cell death, which has been confirmed to promote the occurrence and development of tumors. However, whether cuproptosis-related lncRNA has an impact on the prognosis of squamous cell carcinoma of the head and neck (HNSCC) is still unclear. In total, 501 HNSCC tumor samples and 44 normal were downloaded from the TCGA database. Cuproptosis-related lncRNAs were obtained by co-expressed analysis. We got prognostic lncRNA that was associated with cuproptosis by using univariate Cox regression analysis and LASSO Cox regression. Then we constructed and validated the prognostic signature of HNSCC and analyzed the immune landscape of the signature. The Prognostic Signature is based on 10 cuproptosis-related lncRNAs including AC090587.1, AC004943.2, TTN-AS1, AL162458.1, AC106820.5, AC012313.5, AL132800.1, WDFY3-AS2, CDKN2A-DT, and AL136419.3. The results of overall survival, risk score distribution, and survival status in the low-risk group were better than those in the high-risk group. In addition, all immune checkpoint genes involved were significantly different between the two risk groups (p < 0.05). The risk score was positively correlated with Eosinophils. M0 and M2 phenotype macrophages, mast cells activated, NK cells activated, and negatively related with B cells naive, mast cells resting, plasma cells, CD8T cells, T cells follicular helper, T cells regulatory (Tregs). Consensus clustering was identified in molecular subtypes of HNSC. More high-risk samples concentrated in Cluster1, which had a higher Tumor Immune Dysfunction and Exclusion (TIDE) score and Single Nucleotide Polymorphisms (SNP) alternation than Cluster2. Our study elucidated the correlation between cuproptosis-related lncRNA with prognosis and immune landscape of HNSCC, which may provide references for further research on the exploration of the mechanism and functions of the prognosis for HNSCC.
铜死亡已被确认为一种新型的调节性细胞死亡,已证实其可促进肿瘤的发生和发展。然而,铜死亡相关lncRNA对头颈部鳞状细胞癌(HNSCC)预后是否有影响仍不清楚。从TCGA数据库中总共下载了501个HNSCC肿瘤样本和44个正常样本。通过共表达分析获得铜死亡相关lncRNA。我们使用单变量Cox回归分析和LASSO Cox回归得到了与铜死亡相关的预后lncRNA。然后我们构建并验证了HNSCC的预后特征,并分析了该特征的免疫格局。预后特征基于10个铜死亡相关lncRNA,包括AC090587.1、AC004943.2、TTN-AS1、AL162458.1、AC106820.5、AC012313.5、AL132800.1、WDFY3-AS2、CDKN2A-DT和AL136419.3。低风险组的总生存结果、风险评分分布和生存状态均优于高风险组。此外,两个风险组之间所有涉及的免疫检查点基因均存在显著差异(p<0.05)。风险评分与嗜酸性粒细胞呈正相关。与M0和M2表型巨噬细胞、活化的肥大细胞、活化的NK细胞呈正相关,与幼稚B细胞、静息肥大细胞、浆细胞、CD8T细胞、滤泡辅助性T细胞、调节性T细胞(Tregs)呈负相关。在HNSC的分子亚型中鉴定出了一致性聚类。更多的高风险样本集中在Cluster1中,其肿瘤免疫功能障碍和排除(TIDE)评分以及单核苷酸多态性(SNP)改变均高于Cluster2。我们的研究阐明了铜死亡相关lncRNA与HNSCC预后和免疫格局之间的相关性,这可能为进一步研究HNSCC预后机制和功能提供参考。