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Alteration of liver glycopatterns during cirrhosis and tumor progression induced by HBV

机译:乙肝病毒引起的肝硬化和肿瘤进展过程中肝糖模式的改变

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The incidence of hepatocellular carcinoma (HCC) is closely correlated with hepatitis B virus (HBV)-induced liver cirrhosis. Structural changes in the glycans of serum and tissue proteins are reliable indicators of liver damage. However, little is known about the alteration of liver glycopatterns during cirrhosis and tumor progression induced by HBV infection. This study compared the differential expression of liver glycopatterns in 7 sets of normal pericarcinomatous tissues (PCTs), cirrhotic, and tumor tissues from patients with liver cirrhosis and HCC induced by HBV using lectin microarrays. Fluorescence-based lectin histochemistry and lectin blotting were further utilized to validate and assess the expression and distribution of certain glycans in 9 sets of corresponding liver tissue sections. Eight lectins (e.g., Jacalin and AAL) revealed significant difference in cirrhotic tissues versus PCTs. Eleven lectins (e.g., EEL and SJA) showed significant alteration during cirrhotic and tumor progression. The expression of Gala1-3(Fuca1-2) Gal (EEL) and fucosyltransferase 1 was mainly increasing in the cytoplasm of hepatocytes during PCTs-cirrhotic-tumor tissues progression, while the expression of T antigen (ACA and PNA) was decreased sharply in cytoplasm of tumor hepatocytes. Understanding the precision alteration of liver glycopatterns related to the development of hepatitis, cirrhosis, and tumor induced by HBV infection may help elucidate the molecular mechanisms underlying the progression of chronic liver diseases and develop new antineoplastic therapeutic strategies.
机译:肝细胞癌(HCC)的发生与乙型肝炎病毒(HBV)引起的肝硬化密切相关。血清和组织蛋白聚糖结构的变化是肝损伤的可靠指标。然而,对于由乙肝病毒感染引起的肝硬化和肿瘤进展期间肝糖模式的改变知之甚少。这项研究使用凝集素微阵列比较了HBV诱发的肝硬化和HCC患者的7组正常肝癌组织,肝硬化和肿瘤组织中肝糖模式的差异表达。进一步利用基于荧光的凝集素组织化学和凝集素印迹法来验证和评估9种相应肝脏组织切片中某些聚糖的表达和分布。八种凝集素(例如Jacalin和AAL)显示出肝硬化组织与PCT的显着差异。十一种凝集素(例如EEL和SJA)在肝硬化和肿瘤进展期间显示出明显的变化。在PCTs-肝硬化肿瘤组织进程中,Gala1-3(Fuca1-2)Gal(EEL)和岩藻糖基转移酶1的表达主要在肝细胞的细胞质中增加,而T抗原(ACA和PNA)的表达急剧下降。肿瘤肝细胞的细胞质。了解与由HBV感染引起的肝炎,肝硬化和肿瘤的发展相关的肝糖模式的精确改变,可能有助于阐明慢性肝病进展的分子机制,并开发新的抗肿瘤治疗策略。

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