Department of Neurosurgery, The Affiliated Hospital of Qingdao University, Qingdao City 266000, China.
Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao City 266000, China.
Biomed Res Int. 2022 Sep 25;2022:9957604. doi: 10.1155/2022/9957604. eCollection 2022.
Increasing evidence has shown that necroptosis has enormous significance in the generation and deterioration of cancer, and miRNA molecular markers involved in necroptosis in low-grade gliomas (LGGs) have not been thoroughly reported.
Using the miRNA data of 512 samples from The Cancer Genome Atlas (TCGA), 689 miRNAs from LGG samples were split into high immunity score and low immunity score groups for analysis. The differential miRNAs related to necroptosis were analyzed by univariate Cox regression analysis. On the basis of the outcome of univariate Cox regression analysis, miRNAs with significant differences were selected to construct a multivariate Cox regression model and calculate the risk score. Then, we evaluated whether the risk score could be used as an unaided prognostic factor.
Overall, six differential miRNAs were identified (, , , , , and ). Univariate and multivariate Cox regression analyses were performed, and the index was 0.71. Then, by mixing the risk score with clinicopathological factors, univariate Cox regression (HR: 2.7146, 95% CI: 1.8402-4.0044, < 0.0001) and multivariate Cox regression analyses (HR: 2.3280, 95% CI: 1.5692-3.4536, < 0.001) were performed. The data suggested that the risk score is an unaided prognostic indicator, which is markedly related with the overall survival time of LGG sufferers. Thus, a lower risk score is correlated with better prediction of LGG.
In order to achieve the ultimate goal of improving the living conditions of patients, we established prognostic risk model using 6 miRNAs related to necroptosis, which has the ability to predict the prognosis of LGG. It is possible to further enrich the therapeutic targets for LGG and provide clinical guidance for the treatment of LGG in the future.
越来越多的证据表明,细胞坏死性凋亡在癌症的发生和恶化中具有重要意义,而涉及低级别胶质瘤(LGG)细胞坏死性凋亡的 miRNA 分子标志物尚未得到彻底报道。
利用来自癌症基因组图谱(TCGA)的 512 个样本的 miRNA 数据,将来自 LGG 样本的 689 个 miRNA 分为高免疫评分组和低免疫评分组进行分析。通过单变量 Cox 回归分析对与细胞坏死性凋亡相关的差异 miRNA 进行分析。基于单变量 Cox 回归分析的结果,选择有显著差异的 miRNAs 构建多变量 Cox 回归模型并计算风险评分。然后,我们评估风险评分是否可以作为一个无辅助的预后因素。
总体而言,鉴定出了 6 个差异 miRNA(,,,,,和)。进行单变量和多变量 Cox 回归分析,得出指数为 0.71。然后,通过将风险评分与临床病理因素混合,进行单变量 Cox 回归(HR:2.7146,95%CI:1.8402-4.0044,<0.0001)和多变量 Cox 回归分析(HR:2.3280,95%CI:1.5692-3.4536,<0.001)。数据表明,风险评分是一个无辅助的预后指标,与 LGG 患者的总生存时间明显相关。因此,较低的风险评分与更好的 LGG 预测相关。
为了达到改善患者生活条件的最终目标,我们建立了一个使用与细胞坏死性凋亡相关的 6 个 miRNA 的预后风险模型,该模型能够预测 LGG 的预后。有可能进一步丰富 LGG 的治疗靶点,并为未来 LGG 的治疗提供临床指导。