Department of Gynecological Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Hubei Key Laboratory of Tumor Biological Behaviors, Wuhan, China.
J Cancer Res Clin Oncol. 2023 Oct;149(13):12057-12070. doi: 10.1007/s00432-023-05074-6. Epub 2023 Jul 8.
BACKGROUND: Oral squamous cell carcinoma (OSCC) has been recognized as a frequently occurring oral malignant tumor. Pyroptosis plays an extremely important role in the occurrence and development of cancer, but the role of pyroptosis in OSCC remains unclear. METHODS: OSCC-related data were obtained from the TCGA and GEO databases. A PSscore risk model was constructed through LASSO regression analysis. The GEO database was utilized as the validation set of the model. The "ESTIMATE" and "CIBERSORT" algorithms were utilized to additionally evaluate the relationship between the immune cell score and PSscore. TIDE and IPS algorithms were used to assess patient response to immunotherapy. In addition, Western blot analysis and MTT assay was used to further validate key genes. RESULTS: Comprehensive bioinformatics analysis showed that a low-PSscore had a significant survival advantage, richer immune cell infiltration, more active immune-related pathways, higher TME scores, and lower tumor purity. The results of TIDE and IPS analysis indicated that the high-PSscore group had higher immune escape potential and was less sensitive to immunotherapy. In contrast, the low-PSscore group patients might be more sensitive to PD1 and CTLA4 + PD1 immunotherapy. Univariate and multivariate COX results indicated that PSscore was an independent prognostic factor in OSCC patients. Another important finding is that BAK1 is a potential target of OSCC and is related to the Nod-like receptor signaling pathway. Knockdown of BAK1 can significantly reduce the proliferation of OSCC cells. CONCLUSION: The PSscore model could be utilized as a powerful prognostic indicator and can help in the development of new immunotherapies.
背景:口腔鳞状细胞癌(OSCC)已被认为是一种常见的口腔恶性肿瘤。细胞焦亡在癌症的发生和发展中起着极其重要的作用,但细胞焦亡在 OSCC 中的作用尚不清楚。
方法:从 TCGA 和 GEO 数据库中获取 OSCC 相关数据。通过 LASSO 回归分析构建 PSscore 风险模型。GEO 数据库被用作模型的验证集。利用“ESTIMATE”和“CIBERSORT”算法进一步评估免疫细胞评分与 PSscore 之间的关系。使用 TIDE 和 IPS 算法评估患者对免疫治疗的反应。此外,还使用 Western blot 分析和 MTT 检测进一步验证关键基因。
结果:综合生物信息学分析表明,低 PSscore 具有显著的生存优势,丰富的免疫细胞浸润,更活跃的免疫相关途径,更高的 TME 评分和更低的肿瘤纯度。TIDE 和 IPS 分析结果表明,高 PSscore 组具有更高的免疫逃逸潜力,对免疫治疗的敏感性较低。相比之下,低 PSscore 组患者可能对 PD1 和 CTLA4+PD1 免疫治疗更敏感。单因素和多因素 COX 结果表明 PSscore 是 OSCC 患者的独立预后因素。另一个重要发现是 BAK1 是 OSCC 的潜在靶点,与 Nod-like 受体信号通路有关。敲低 BAK1 可显著降低 OSCC 细胞的增殖。
结论:PSscore 模型可作为一种强大的预后指标,并有助于开发新的免疫疗法。
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