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Higher expression of cell division cycle-associated protein 5 predicts poorer survival outcomes in hepatocellular carcinoma

机译:细胞分裂周期相关蛋白5的表达更高的表达预测肝细胞癌中的较差的存活结果

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摘要

The upregulation of cell division cycle associated protein 5 (CDCA5) has been observed in various cancer types. However, the prognostic value of CDCA5 and its underlying mechanism contributing to tumorigenesis in hepatocellular carcinoma (HCC) remain poorly understood. We used tissue microarray (TMA) to evaluate the prognosis of 304 HCC samples based on their CDCA5 expression, and analyzed the genomic features correlated with CDCA5 by using dataset from The Cancer Genome Atlas (TCGA). Compared with adjacent normal tissues, increased expression of CDCA5 was found in HCC tissues. Moreover, higher expression of CDCA5 was associated with inferior OS and DFS outcomes in HCC patients. The enrichment plots showed that the gene signatures in cell cycle, DNA replication and p53 pathways were enriched in patients with higher CDCA5 expression. Meanwhile, statistically higher mutations burdens in TP53 could also be observed in CDCA5-high patients. Integrative analysis based on miRNAseq and methylation data demonstrated a potential association between CDCA5 expression and epigenetic changes. In conclusion, our study provided the evidence of CDCA5 as an oncogenic promoter in HCC and the potential function of CDCA5 in affecting tumor microenvironment.
机译:在各种癌症类型中观察到细胞分裂周期相关蛋白5(CDCA5)的上调。然而,CDCA5的预后价值及其在肝细胞癌(HCC)中有助于肿瘤发生的潜在机制仍然明确。我们使用组织微阵列(TMA)根据其CDCA5表达评估304个HCC样品的预后,并通过使用来自癌症基因组Atlas(TCGA)的数据集来分析与CDCA5相关的基因组特征。与相邻的正常组织相比,在HCC组织中发现CDCA5的增加。此外,CDCA5的更高表达与HCC患者的差异次级和DFS结果相关。富集图表明,细胞周期,DNA复制和P53途径中的基因签名在较高的CDCA5表达患者中富集。同时,在CDCA5高患者中也可以观察到TP53中的统计学上更高的突变。基于MIRNASEQ和甲基化数据的整合分析表明了CDCA5表达和表观遗传变化之间的潜在关联。总之,我们的研究提供了CDCA5作为HCC的致癌促进剂的证据以及CDCA5在影响肿瘤微环境中的潜在功能。

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