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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >A poor prognosis in human hepatocellular carcinoma is associated with low expression of DPP4
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A poor prognosis in human hepatocellular carcinoma is associated with low expression of DPP4

机译:人类肝细胞癌的预后差与DPP4的低表达有关

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This study aimed to explore the prognostic role of dipeptidyl peptidase 4 (DPP4) expression in hepatocellular carcinoma (HCC). DPP4 expression was measured in formalin-fixed paraffin-embedded specimens that were gathered from 327 HCC patients. Immunohistochemistry analyses were utilized to examine DPP4 expression characteristics and prognostic values (overall survival (OS) and time to recurrence) of DDP4 in HCC tissues. In addition, a patient-derived xenograft (PDX) model was used to assess the correlation between DPP4 expression and tumor growth in vivo. DPP4 was expressed in low levels in HCC tissues in contrast to paired peritumoral tissues (38 cases were down-regulated in a total of 59 cases, 64.4%. P=0.0202). DPP4 expression was significantly correlated with TNM stage (P=0.038), tumor number (P=0.035), and vascular invasion (P=0.024), and significantly reduced in patients who were in TNM stages II and III-V, with multiple tumors, and with microvascular invasion compared to patients with TNM stage I, single tumor, and no microvascular invasion. Notably, HCC tissues with low expression of DPP4 had poor OS (P=0.016) compared with HCC tissues with high expression of DPP4, and results from PDX model showed that tumor growth was significantly faster in HCC patients that lowly expressed DPP4 compared to those with highly expressed DPP4. Our findings suggested that low levels of DPP4 could impact the aggressiveness of HCC and contribute to a poor prognosis.
机译:该研究旨在探讨二肽基肽酶4(DPP4)表达在肝细胞癌(HCC)中的预后作用。在福尔马林固定的石蜡包埋的标本中测量DPP4表达,从327例HCC患者收集。利用免疫组织化学分析来检查HCC组织中DDP4的DPP4表达特征和预后值(整体存活率(OS)和时间)。此外,使用患者衍生的异种移植物(PDX)模型来评估体内DPP4表达和肿瘤生长之间的相关性。与双HCC组织的低水平表达DPP4与配对的腹膜组织相比(38例,共59例,64.4%。P = 0.0202)。 DPP4表达与TNM阶段显着相关(P = 0.038),肿瘤数(p = 0.035)和血管侵袭(p = 0.024),并且在TNM阶段II和III-V的患者中显着降低,具有多种肿瘤与TNM阶段I,单一肿瘤和无微血管侵袭的患者相比,微血管侵袭。值得注意的是,与具有高表达DPP4的HCC组织的HCC表达低表达的HCC组织具有差(P = 0.016),并且PDX模型的结果显示HCC患者的肿瘤生长明显更快,与那些差异的DPP4低表达DPP4高度表达的DPP4。我们的研究结果表明,低水平的DPP4可能会影响HCC的侵略性并有助于预后差。

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