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一种用于透明细胞肾细胞癌的新型巨噬细胞分化相关预后模型的系统构建与验证

Systematic Construction and Validation of a Novel Macrophage Differentiation-Associated Prognostic Model for Clear Cell Renal Cell Carcinoma.

作者信息

Liu Chen, Zhang Xuhui, Hu Caoyang, Liang Xuezhi, Cao Xiaoming, Wang Dongwen

机构信息

First Clinical Medical College, Shanxi Medical University, Taiyuan, China.

Department of Urology, First Hospital of Shanxi Medical University, Taiyuan, China.

出版信息

Front Genet. 2022 Jun 14;13:877656. doi: 10.3389/fgene.2022.877656. eCollection 2022.

Abstract

Clear cell renal cell carcinoma (ccRCC) is a malignant tumor of the human urinary system. Macrophage differentiation is associated with tumorigenesis. Therefore, exploring the prognostic value of macrophage differentiation-associated genes (MDGs) may contribute to better clinical management of ccRCC patients. The RNA sequence data of ccRCC were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed MDGs were unveiled in ccRCC and normal samples. The prognostic model was established according to the univariate and multivariate Cox regression analyses. By combining clinico-pathological features and prognostic genes, a nomogram was established to predict individual survival probability. The Tumor Immune Estimation Resource (TIMER) database was utilized to analyze the correlation between prognostic genes and immune infiltrating cells. Eventually, the mRNA and protein expression levels of prognostic genes were verified. A total of 52 differentially expressed prognosis-related MDGs were identified in ccRCC. Afterward, a six-gene prognostic model (ABCG1, KDF1, KITLG, TGFA, HAVCR2, and CD14) was constructed through the Cox analysis. The overall survival in the high-risk group was relatively poor. Moreover, the risk score was identified as an independent prognostic factor. We constructed a prognostic nomogram with a well-fitted calibration curve based on risk score and clinical data. Furthermore, the prognostic genes were significantly related to the level of immune cell infiltration including B cells, CD8+T cells, CD4+T cells, macrophages, neutrophils, and dendritic cells. Finally, the mRNA expression of prognostic genes in clinical ccRCC tissues showed that the ABCG1, HAVCR2, CD14, and TGFA mRNA in tumor samples were increased compared with the adjacent control tissue samples, while KDF1 and KITLG were decreased, which was consistent with the verification results in the GSE53757. In conclusion, this study identified and validated a macrophage differentiation-associated prognostic model for ccRCC that could be used to predict the outcomes of the ccRCC patients.

摘要

透明细胞肾细胞癌(ccRCC)是人类泌尿系统的一种恶性肿瘤。巨噬细胞分化与肿瘤发生相关。因此,探索巨噬细胞分化相关基因(MDGs)的预后价值可能有助于改善ccRCC患者的临床管理。ccRCC的RNA序列数据来自癌症基因组图谱(TCGA)数据库。在ccRCC和正常样本中发现了差异表达的MDGs。根据单变量和多变量Cox回归分析建立预后模型。通过结合临床病理特征和预后基因,建立了一个列线图来预测个体生存概率。利用肿瘤免疫评估资源(TIMER)数据库分析预后基因与免疫浸润细胞之间的相关性。最终,验证了预后基因的mRNA和蛋白表达水平。在ccRCC中总共鉴定出52个差异表达的预后相关MDGs。随后,通过Cox分析构建了一个六基因预后模型(ABCG1、KDF1、KITLG、TGFA、HAVCR2和CD14)。高危组的总生存期相对较差。此外,风险评分被确定为独立的预后因素。我们基于风险评分和临床数据构建了一个具有良好拟合校准曲线的预后列线图。此外,预后基因与包括B细胞、CD8 + T细胞、CD4 + T细胞、巨噬细胞、中性粒细胞和树突状细胞在内的免疫细胞浸润水平显著相关。最后,临床ccRCC组织中预后基因的mRNA表达表明,与相邻对照组织样本相比,肿瘤样本中的ABCG1、HAVCR2、CD14和TGFA mRNA增加,而KDF1和KITLG降低,这与GSE53757中的验证结果一致。总之,本研究鉴定并验证了一种用于ccRCC的巨噬细胞分化相关预后模型,可用于预测ccRCC患者的预后。

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