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上皮细胞黏附分子在异型增生结节和肝细胞癌中的表达及作用。

Expression and role of epithelial cell adhesion molecule in dysplastic nodule and hepatocellular carcinoma.

机构信息

Department of Pathology, Chonbuk National University, Medical School, and Research Institute for Endocrine Sciences, Jeonju, Republic of Korea.

出版信息

Int J Oncol. 2012 Dec;41(6):2150-8. doi: 10.3892/ijo.2012.1631. Epub 2012 Sep 19.

Abstract

Epithelial cell adhesion molecule (EpCAM) has been proposed as a marker for cancer stem cells in human hepatocellular carcinoma (HCC). However, the function and clinical significance of EpCAM in HCC is largely unknown. We examined EpCAM expression and localization in 28 dysplastic nodules (DNs) and their corresponding cirrhotic nodules, 79 HCC tissue sections and 132 HCC tissue microarray cores by immunohistochemistry and determined the relationship to clinicopathologic findings. We also examined the role of EpCAM in HCC using synthetic small interfering RNA to silence EpCAM gene expression in Huh-7 cells. EpCAM expression was very rare in DNs but dominantly appeared in a distinctly nodular type of small HCC. Expression of EpCAM was observed in 39% (31/79) of HCC tissue sections and in 34.1% (45/132) of tissue microarray sections. EpCAM expression in HCC was significantly associated with high tumor grade and serum α-fetoprotein level. Silencing EpCAM gene expression significantly decreased the proliferative activity and invasiveness of HCC cells. EpCAM expression was an independent prognostic factor for survival in patients with T1 HCC. The data indicate that EpCAM expression occurs at distinct nodular stage of HCC and could play an important role in HCC progression.

摘要

上皮细胞黏附分子 (EpCAM) 已被提议作为人类肝细胞癌 (HCC) 中癌症干细胞的标志物。然而,EpCAM 在 HCC 中的功能和临床意义在很大程度上尚不清楚。我们通过免疫组织化学检查了 28 个异型增生结节 (DN) 及其相应的肝硬化结节、79 个 HCC 组织切片和 132 个 HCC 组织微阵列核心中的 EpCAM 表达和定位,并确定了其与临床病理发现的关系。我们还使用合成的小干扰 RNA 检查了 EpCAM 在 HCC 中的作用,以沉默 Huh-7 细胞中的 EpCAM 基因表达。EpCAM 在 DNs 中表达非常罕见,但在明显的小结节型小 HCC 中明显出现。在 39%(31/79)的 HCC 组织切片和 34.1%(45/132)的组织微阵列切片中观察到 EpCAM 的表达。EpCAM 在 HCC 中的表达与高肿瘤分级和血清 α-胎蛋白水平显著相关。沉默 EpCAM 基因表达显著降低了 HCC 细胞的增殖活性和侵袭性。EpCAM 表达是 T1 HCC 患者生存的独立预后因素。数据表明,EpCAM 表达发生在 HCC 的明显结节阶段,可能在 HCC 进展中发挥重要作用。

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