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Clinicopathological characteristics and liver stem cell marker expression in hepatocellular carcinoma involving bile duct tumor thrombi

机译:胆管肿瘤血栓性肝细胞癌的临床病理特征及肝干细胞标志物的表达

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摘要

The aim of this study was to analyze the clinicopathological characteristics and expression of liver stem cell markers of hepatocellular carcinoma (HCC) involving bile duct tumor thrombi (BDTT). A total of 35 patients with HCC and BDTT in a consecutive series of HCC patients who underwent surgical treatment were studied retrospectively and compared with 916 patients without BDTT from the same series. Clinicopathological characteristics, overall survival (OS), and tumor expression of liver stem cell markers CD133, CD90, EpCAM, CK19, VEGF, and C-kit were compared between the two patient groups. Analysis was performed for the entire patient groups as well as for 35 pairs of patients with or without BDTT matched by propensity score. HCC patients with BDTT tended to have smaller tumors than those without BDTT, as well as a higher probability of having poorly differentiated tumor, Child-Pugh class B, liver cirrhosis, and microvascular invasion. Tumor tissue in patients with BDTT showed significantly higher expression rates of all liver stem cell markers examined. OS was significantly lower for patients with BDTT at 1 year (69 vs 84 %), 3 years (37 vs 64 %), and 5 years (20 vs 55 %) (P<0.001). Patients with HCC and BDTT show lower OS than patients without BDTT. The higher frequency of liver stem cell marker expression in the presence of BDTT suggests that such stem cells may play a role in the pathogenesis of this form of HCC.
机译:这项研究的目的是分析涉及胆管肿瘤血栓(BDTT)的肝细胞癌(HCC)的肝干细胞标志物的临床病理特征和表达。回顾性分析了连续接受手术治疗的HCC患者系列中的35例HCC和BDTT患者,并将其与同一系列中916例无BDTT的患者进行了比较。比较两组患者的肝干细胞标志物CD133,CD90,EpCAM,CK19,VEGF和C-kit的临床病理特征,总生存期(OS)和肿瘤表达。对整个患者组以及35对有或没有BDTT的患者按倾向评分进行分析。患有BDTT的HCC患者往往比没有BDTT的患者肿瘤更小,而且分化不良的肿瘤,Child-Pugh B级,肝硬化和微血管浸润的可能性更高。 BDTT患者的肿瘤组织显示所有检查的肝干细胞标记物的表达率均显着较高。 BDTT患者在1年时(69 vs 84%),3年(37 vs 64%)和5年(20 vs 55%)的OS显着降低(P <0.001)。患有HCC和BDTT的患者的OS低于没有BDTT的患者。在BDTT存在下,肝干细胞标志物表达的频率更高,表明此类干细胞可能在这种形式的HCC的发病机理中起作用。

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