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Correlation between biological marker expression and fluorine-18 fluorodeoxyglucose uptake in hepatocellular carcinoma.

肝细胞癌生物标志物表达与18-F脱氧葡萄糖摄取的关系

Mano Y,Aishima S,Kubo Y,Tanaka Y,Motomura T,Toshima T,Shirabe K,Baba S,Maehara Y,Oda Y

Abstract

This study investigated the association between several biological markers and fluorine-18 fluorodeoxyglucose (FDG) uptake in patients with hepatocellular carcinoma.
Forty-two patients with hepatocellular carcinoma who underwent FDG positron emission tomography were included in the study. Tumor sections were immunohistochemically stained for phosphorylated signal transducer and activator of transcription 3 (pSTAT3), hypoxia-inducible factor 1α (HIF1α), glucose transporter 1 (GLUT1), GLUT2, GLUT3, and GLUT4.
The high standardized uptake value (SUV) group showed larger tumor size, more frequent vascular invasion, and poorer differentiation compared with the low SUV group. The high SUV group also showed significantly higher immunohistochemical expression of pSTAT3, HIF1α, and GLUT1. The GLUT1 high-expression group showed higher α-fetoprotein (a tumor marker) and poorer differentiation than did the GLUT1 low-expression group.
Our study indicates that FDG uptake is associated with the expression of pSTAT3, HIF1α, and GLUT1 in hepatocellular carcinoma. The expression of these proteins shows a correlation with poor differentiation and vascular invasion.

摘要

本研究调查了肝细胞癌患者几种生物标志物表达和18F-脱氧葡萄糖(FDG)摄取之间的关系。

本研究纳入了42例经FDG正电子发射断层扫描的肝细胞癌患者。患者肿瘤组织切片进行了磷酸化信号转导与转录激活因子3(pSTAT3)、缺氧诱导因子1α(HIF1α)和葡萄糖转运蛋白1(GLUT1)、GLUT2、GLUT3及GLUT4免疫组化染色。

与标准化摄取值(SUV)低的组相比,高SUV组肿瘤体积较大、血管侵犯更常见且分化更差。高SUV组也显示pSTAT3、HIF1α和GLUT1免疫表达明显增高。GLUT1高表达与低表达组相比,血清α甲胎蛋白(肿瘤标记物)水平增高并且分化较差。

我们的研究表明,肝细胞癌FDG摄取与pSTAT3、HIF1α和GLUT1表达相关。这些蛋白的表达与肿瘤分化差和血管浸润相关。

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