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Association between expression of Carboxypeptidase 4 and stem cell markers and their clinical significance in liver cancer development

机译:羧肽酶4的表达与干细胞标志物的关系及其在肝癌发展中的临床意义

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摘要

The development of liver cancer would undergo a sequential progression from chronic inflammatory liver disease, cirrhosis to neoplasia. During these pathophysiological changes, abnormal liver microenvironment might induce the hepatocytes to die, abnormally proliferate and initiate cancer stem cells. Metallocarboxypeptidases (MCPs) involved in multiple biological functions including inflammation, fibrosis and stem cell niche formation. This study aimed to evaluate the expression of carboxypeptidase 4 (CPA4) in hepatitis, liver cirrhosis and liver cancer tissues, and revealed its clinical significance in liver cancer progression. We firstly found that the CPA4 levels in tissues were significantly higher in liver cancer patients than those in other three groups. Then, elevated levels of CPA4 was observed in 57/100 (57%) liver cancer samples, and significantly correlated with Grade and Stage. We also identified a significant positive correlation between aberrant elevation of CPA4 and overexpression of stem cell markers including CD90, AFP and CD34 with follow-up data (n=100). Further Kaplan-Meier analysis confirmed that high levels of CPA4 and CD90 were significant predictors of poor overall survival. Multivariate Cox regression model showed that CPA4 was an independent prognostic factor for patients with liver cancer. This study demonstrated for the first time that high CPA4 expression was closely correlated with hepatocarcinogenesis, and might be used as an independent poor prognostic factor in liver cancer.
机译:肝癌的发展将经历从慢性炎症性肝病,肝硬化到瘤形成的顺序发展。在这些病理生理变化过程中,异常的肝微环境可能会诱导肝细胞死亡,异常增殖并引发癌症干细胞。金属羧肽酶(MCPs)参与多种生物学功能,包括炎症,纤维化和干细胞小生境的形成。这项研究旨在评估羧肽酶4(CPA4)在肝炎,肝硬化和肝癌组织中的表达,并揭示其在肝癌进展中的临床意义。我们首先发现,肝癌患者组织中的CPA4水平明显高于其他三组。然后,在57/100(57%)肝癌样本中观察到CPA4水平升高,并且与等级和阶段显着相关。我们还发现CPA4异常升高与干细胞标志物(包括CD90,AFP和CD34)的过表达之间存在显着正相关,并具有后续数据(n = 100)。进一步的Kaplan-Meier分析证实,高水平的CPA4和CD90是整体生存不良的重要预测指标。多元Cox回归模型显示CPA4是肝癌患者的独立预后因素。这项研究首次证明了高CPA4表达与肝癌发生密切相关,并且可能被用作肝癌的独立不良预后因素。

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