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Overexpression of BUB1B CCNA2 CDC20 and CDK1 in tumor tissues predicts poor survival in pancreatic ductal adenocarcinoma

机译:BUB1BCCNA2CDC20和CDK1在肿瘤组织中的过表达预示胰腺导管腺癌的不良生存

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摘要

Overexpressed genes in tumors usually contributed to aggressiveness in pancreatic ductal adenocarcinoma (PDAC). Using Gene Expression Omnibus (GEO) profiles including , , and , we detected overexpressed genes in tumors with R program, which were enriched by Kyoto Encyclopedia of Genes and Genomes (KEGG), Gene ontology (GO), and Reactome pathway databases. Then, we performed a survival analysis of enriched genes based on TCGA profile. Our results revealed that high BUB1B, CCNA2, CDC20, and CDK1 expression in tumors was significantly associated with worse overall survival (OS) (Log rank P=0.00338, P=0.0447, P=0.00965, and P=0.00479, respectively), which was validated using a Kaplan–Meier plotter with a median cutoff (Log rank P=0.028, P=0.0035, P=0.039, and P=0.0033, respectively). Moreover, overexpression of BUB1B, CCNA2, CDC20, and CDK1 in tumor tissues was significantly associated with disease-free survival (DFS) in PDAC patients (Log rank P=0.00565, P=0.0357, P=0.00104, and P=0.00121, respectively). BUB1B, CCNA2, CDC20, and CDK1 were significantly overexpressed in deceased PDAC patients (all P<0.01) and in patients with recurrence/disease progression (all P<0.05). In addition, PDAC patients with neoplasms of histologic grade G3-4 had significantly higher BUB1B, CCNA2 and CDC20 levels (all P<0.05). In conclusion, the up-regulation of BUB1B, CCNA2, CDC20, CDK1, and WEE1 in tumor tissues are associated with worse OS and DFS in PDAC and is correlated with advanced tumor stage and tumor development.
机译:肿瘤中过表达的基因通常有助于胰腺导管腺癌(PDAC)的侵袭性。使用包括,和在内的Gene Expression Omnibus(GEO)配置文件,我们使用R程序检测了肿瘤中过表达的基因,这些基因已被《京都议定书》(Kyoto Encyclopedia of Genes and Genomes,KEGG),基因本体论(GO)和Reactome途径数据库所丰富。然后,我们根据TCGA谱对丰富的基因进行了生存分析。我们的结果表明,肿瘤中高的BUB1B,CCNA2,CDC20和CDK1表达与较差的总体生存率(OS)显着相关(分别为Log Rank P = 0.00338,P = 0.0447,P = 0.00965和P = 0.00479),使用具有中位数截止值的Kaplan–Meier绘图仪(分别对数秩P = 0.028,P = 0.0035,P = 0.039和P = 0.0033)进行了验证。此外,在肿瘤组织中BUB1B,CCNA2,CDC20和CDK1的过表达与PDAC患者的无病生存率(DFS)显着相关(分别为Log Rank P = 0.00565,P = 0.0357,P = 0.00104和P = 0.00121)。 )。在已故的PDAC患者中,BUB1B,CCNA2,CDC20和CDK1显着过表达(所有P <0.01)和复发/疾病进展患者(所有P <0.05)。另外,组织学分级为G3-4的PDAC肿瘤患者的BUB1B,CCNA2和CDC20水平显着升高(所有P <0.05)。总之,肿瘤组织中BUB1B,CCNA2,CDC20,CDK1和WEE1的上调与PDAC中较差的OS和DFS相关,并且与晚期肿瘤分期和肿瘤发展相关。

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