Department of Internal Medicine, Chungnam National University School of Medicine, Daejeon, Korea.
Department of Pathology, Chungnam National University School of Medicine, Daejeon, Korea.
Gut Liver. 2014 Jan;8(1):79-87. doi: 10.5009/gnl.2014.8.1.79. Epub 2014 Jan 13.
BACKGROUND/AIMS: The current study examines the expression of molecular biomarkers in hepatocellular carcinoma (HCC) and whether these findings correlate with the clinicopathologic features of the disease and patient survival.
We analyzed the immunohistochemical expression of p53, mammalian target of rapamycin (mTOR), c-Met, and insulin-like growth factor 1 receptor (IGF-1R) heat shock protein 70 (HSP70) with the clinicopathologic features of 83 HCCs.
p53 expression was higher in the male patients with undifferentiated histological tumor grades, cirrhosis, and portal vein invasion. High 48 c-Met expression correlated with cirrhosis, and high mTOR expression correlated with the tumor grade and cirrhosis. High IGF-1R expression correlated with the tumor grade and cirrhosis. A multivariate analysis identified a significant relationship between the high expression of p53, tumor grade, and portal vein invasion. In addition, a high expression of mTOR was related to tumor grade and cirrhosis, and a high expression of HSP70 was related to portal vein invasion in a multivariate analysis. The Kaplan-Meier survival curve for patients with high versus low Edmondson grades and p53 expression was statistically significant.
p53, mTOR, and IGF-1R expression correlated with the Edmondson tumor grade in a univariate analysis, while p53 and mTOR correlated with the Edmondson tumor grade in a multivariate analysis. In addition, the tumor grade was found to predict survival. p53 was primarily related to the clinicopathologic features compared to other markers, and it is a poor prognostic factor of survival.
背景/目的:本研究检测了肝癌(HCC)中分子生物标志物的表达情况,并探讨了这些标志物的表达与疾病的临床病理特征及患者生存的关系。
我们分析了 83 例 HCC 组织中 p53、哺乳动物雷帕霉素靶蛋白(mTOR)、c-Met、胰岛素样生长因子 1 受体(IGF-1R)和热休克蛋白 70(HSP70)的免疫组化表达,并结合临床病理特征进行分析。
p53 表达在未分化组织学肿瘤分级、肝硬化和门静脉侵犯的男性患者中较高。48 例 c-Met 高表达与肝硬化相关,mTOR 高表达与肿瘤分级和肝硬化相关。IGF-1R 高表达与肿瘤分级和肝硬化相关。多变量分析发现,p53 高表达、肿瘤分级和门静脉侵犯之间存在显著关系。此外,多变量分析显示,mTOR 高表达与肿瘤分级和肝硬化相关,HSP70 高表达与门静脉侵犯相关。Kaplan-Meier 生存曲线分析显示,高表达 p53 的患者与低 Edmondson 分级和 p53 表达的患者之间的生存存在显著差异。
p53、mTOR 和 IGF-1R 的表达与单变量分析中的 Edmondson 肿瘤分级相关,而 p53 和 mTOR 与多变量分析中的 Edmondson 肿瘤分级相关。此外,肿瘤分级被发现可预测患者的生存。与其他标志物相比,p53 主要与临床病理特征相关,是预后不良的因素。