Low expression of fatty acid oxidation related gene ACADM indicates poor prognosis of renal clear cell carcinoma and is related to tumor immune infiltration

被引:1
作者
Qiu, Jiechuan [1 ]
Yang, Tianmin [1 ]
Sun, Yanning [2 ]
Sun, Kai [2 ]
Xu, Yingkun [3 ]
Xia, Qinghua [1 ]
机构
[1] Shandong First Med Univ, Dept Urol, Shandong Prov Hosp, Jinan 250021, Peoples R China
[2] Shandong Univ, Shandong Prov Hosp, Cheeloo Coll Med, Dept Urol, Jinan 250021, Peoples R China
[3] Chongqing Med Univ, Affiliated Hosp 1, Dept Breast & Thyroid Surg, Chongqing 400042, Peoples R China
基金
中国国家自然科学基金;
关键词
Kidney renal clear cell carcinoma; Acyl-CoA dehydrogenase medium chain; Immune infiltration; Fatty acid oxidation; Prognosis; DEHYDROGENASE-DEFICIENCY; CANCER; SUPPRESSION; CCRCC;
D O I
10.32604/or.2023.030462
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This research aims to identify the key fatty acid beta-oxidation (FAO) genes that are altered in kidney renal clear cell carcinoma (KIRC) and to analyze the role of these genes in KIRC. The Gene Expression Omnibus (GEO) and FAO datasets were used to identify these key genes. Wilcoxon rank sum test was used to assess the levels of acylCoA dehydrogenase medium chain (ACADM) between KIRC and non-cancer samples. The logistic regression and Wilcoxon rank sum test were used to explore the association between ACADM and clinical features. The diagnostic performance of ACADM for KIRC was assessed using a diagnostic receiver operating characteristic (ROC) curve. The co-expressed genes of ACADM were identified in LinkedOmics database, and their function and pathway enrichment were analyzed. The correlation between ACADM expression level and immune infiltration was analyzed by Gene Set Variation Analysis (GSVA) method. Additionally, the proliferation, migration, and invasion abilities of KIRC cells were assessed after overexpressing ACADM. Following differential analysis and intersection, we identified six hub genes, including ACADM. We found that the expression level of ACADM was decreased in KIRC tissues and had a better diagnostic effect (AUC = 0.916). Survival analysis suggested that patients with decreased ACADM expression had a worse prognosis. According to correlation analysis, a variety of clinical features were associated with the expression level of ACADM. By analyzing the infiltration level of immune cells, we found that ACADM may be related to the enrichment of immune cells. Finally, ACADM overexpression inhibited proliferation, migration, and invasion of KIRC cells. In conclusion, our findings suggest that reduced ACADM expression in KIRC patients is indicative of poor prognosis. These results imply that ACADM may be a diagnostic and prognostic marker for individuals with KIRC, offering a reference for clinicians in diagnosis and treatment.
引用
收藏
页码:545 / 561
页数:17
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