Fan Weiqiang, Ma Huan, Jin Bin
Department of Organ Transplantation, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, P.R. China.
Oncol Lett. 2022 May;23(5):146. doi: 10.3892/ol.2022.13266. Epub 2022 Mar 15.
Hepatocellular carcinoma (HCC) is one of the most frequently encountered malignant tumor types and to improve its treatment, effective prognostic biomarkers are urgently required. Cell cycle dysregulation is a significant feature of cancer progression. The aim of the present study was to estimate the expression levels of forkhead box protein M1 (FOXM1) and polo-like kinase 1 (PLK1), both of which have essential roles in cell cycle regulation, and determine their prognostic value in HCC. To this end, FOXM1 and PLK1 expression levels were assessed in The Cancer Genome Atlas and International Cancer Genome Consortium Japan HCC cohorts, and the associations between their co-expression were determined via Pearson's correlation analysis. Furthermore, the overall survival and disease-free survival in these cohorts for different FOXM1 and PLK1 expression statuses were analyzed. knockdown experiments were also performed using Huh7 cells. The results obtained indicated overexpression of FOXM1 and PLK1 in HCC tumor tissues as well as a positive correlation between FOXM1 and PLK1 expression. The results also suggested that both FOXM1 and PLK1 are required for HCC cell proliferation. In addition, upregulation of FOXM1 and PLK1 was indicated to be associated with poor prognosis of patients with HCC. However, only their coordinated overexpression was identified as an independent prognostic factor for HCC.
肝细胞癌(HCC)是最常见的恶性肿瘤类型之一,为改善其治疗效果,迫切需要有效的预后生物标志物。细胞周期失调是癌症进展的一个显著特征。本研究的目的是评估在细胞周期调控中起重要作用的叉头框蛋白M1(FOXM1)和 polo样激酶1(PLK1)的表达水平,并确定它们在HCC中的预后价值。为此,在癌症基因组图谱和国际癌症基因组联盟日本HCC队列中评估了FOXM1和PLK1的表达水平,并通过Pearson相关性分析确定了它们共表达之间的关联。此外,分析了这些队列中不同FOXM1和PLK1表达状态下的总生存期和无病生存期。还使用Huh7细胞进行了敲低实验。获得的结果表明,HCC肿瘤组织中FOXM1和PLK1过表达,以及FOXM1和PLK1表达之间呈正相关。结果还表明,HCC细胞增殖需要FOXM1和PLK1。此外,FOXM1和PLK1的上调表明与HCC患者的不良预后相关。然而,只有它们的协同过表达被确定为HCC的独立预后因素。