Wan Bangbei, Huang Yuan, Liu Bo, Lu Likui, Lv Cai
Urology, Haikou Municipal People's Hospital and Central South University Xiangya Medical College Affiliated Hospital, Haikou, China.
Neurology, Haikou Municipal People's Hospital and Central South University Xiangya Medical College Affiliated Hospital, Haikou, China.
PeerJ. 2019 Sep 16;7:e7718. doi: 10.7717/peerj.7718. eCollection 2019.
Aurora kinase B () is an important carcinogenic factor in various tumors, while its role in clear cell renal cell carcinoma (ccRCC) still remains unclear. This study aimed to investigate its prognostic value and mechanism of action in ccRCC.
Gene expression profiles and clinical data of ccRCC patients were downloaded from The Cancer Genome Atlas database. R software was utilized to analyze the expression and prognostic role of in ccRCC. Gene set enrichment analysis (GSEA) was used to analyze related signaling pathways in ccRCC.
was expressed at higher levels in ccRCC tissues than normal kidney tissues. Increased expression in ccRCC correlated with high histological grade, pathological stage, T stage, N stage and distant metastasis (M stage). Kaplan-Meier survival analysis suggested that high expression patients had a worse prognosis than patients with low expression levels. Multivariate Cox analysis showed that expression is a prognostic factor of ccRCC. GSEA indicated that genes involved in autoimmune thyroid disease, intestinal immune network for IgA production, antigen processing and presentation, cytokine-cytokine receptor interaction, asthma, etc., were differentially enriched in the high expression phenotype.
is a promising biomarker for predicting prognosis of ccRCC patients and a potential therapeutic target. In addition, might regulate progression of ccRCC through modulating intestinal immune network for IgA production and cytokine-cytokine receptor interaction, etc. signaling pathways. However, more research is necessary to validate the findings.
极光激酶B(Aurora kinase B,AURKB)是多种肿瘤中重要的致癌因子,但其在肾透明细胞癌(ccRCC)中的作用仍不清楚。本研究旨在探讨其在ccRCC中的预后价值及作用机制。
从癌症基因组图谱数据库下载ccRCC患者的基因表达谱和临床数据。利用R软件分析AURKB在ccRCC中的表达及预后作用。采用基因集富集分析(GSEA)分析ccRCC中与AURKB相关的信号通路。
AURKB在ccRCC组织中的表达水平高于正常肾组织。ccRCC中AURKB表达增加与高组织学分级、病理分期、T分期、N分期和远处转移(M分期)相关。Kaplan-Meier生存分析表明,AURKB高表达患者的预后比低表达患者差。多因素Cox分析显示,AURKB表达是ccRCC的一个预后因素。GSEA表明,参与自身免疫性甲状腺疾病、IgA产生的肠道免疫网络、抗原加工和呈递、细胞因子-细胞因子受体相互作用、哮喘等的基因在AURKB高表达表型中差异富集。
AURKB是预测ccRCC患者预后的一个有前景的生物标志物和潜在的治疗靶点。此外,AURKB可能通过调节IgA产生的肠道免疫网络和细胞因子-细胞因子受体相互作用等信号通路来调节ccRCC的进展。然而,需要更多的研究来验证这些发现。