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EBAG9/RCAS1在肝细胞癌中的表达:与肿瘤去分化和增殖的相关性

EBAG9/RCAS1 expression in hepatocellular carcinoma: correlation with tumour dedifferentiation and proliferation.

作者信息

Aoki T, Inoue S, Imamura H, Fukushima J, Takahashi S, Urano T, Hasegawa K, Ogushi T, Ouchi Y, Makuuchi M

机构信息

Division of Hepato-Biliary-Pancreatic and Transplantation Surgery, Department of Surgery, University of Tokyo, Tokyo, Japan.

出版信息

Eur J Cancer. 2003 Jul;39(11):1552-61. doi: 10.1016/s0959-8049(03)00362-9.

Abstract

The oestrogen-responsive gene, EBAG9, whose product is identical to the cancer cell surface antigen RCAS1, is reported to be associated with tumour progression and invasiveness in various carcinomas. In this study, we examined the expression of EBAG9/RCAS1 in hepatocellular carcinoma (HCC), with special reference to its relationship with the stepwise evolution of HCC. Expression was examined by immunohistochemistry and western blotting analysis in 143 HCCs, as well as in non-cancerous liver tissues. After which, the association between enhanced EBAG9/RCAS1 expression and various clinicopathological parameters including Ki-67 labelling index (LI), a marker of proliferative activity, was evaluated. There was a constant low level of EBAG9/RCAS1 expression in non-cancerous liver tissues, with a regular cytoplasmic distribution. Positive immunoreactivity for EBAG9/RCAS1 was detected on the surface and in the cytoplasm of 84 HCC tumours, with an irregular staining pattern. Enhanced EBAG9/RCAS1 expression was correlated with a lower degree of differentiation and Ki-67 LI. Interestingly, expression was enhanced specifically in the less differentiated lesions within 'nodule-in-nodule' tumours. In conclusion, EBAG9/RCAS1 was associated with HCC tumour dedifferentiation and increased proliferative activity. Its exact functional role remains to be established.

摘要

雌激素反应基因EBAG9,其产物与癌细胞表面抗原RCAS1相同,据报道在多种癌症中与肿瘤进展和侵袭性相关。在本研究中,我们检测了EBAG9/RCAS1在肝细胞癌(HCC)中的表达,并特别关注其与HCC逐步演变的关系。通过免疫组织化学和蛋白质印迹分析检测了143例HCC以及非癌性肝组织中EBAG9/RCAS1的表达。之后,评估了EBAG9/RCAS1表达增强与包括增殖活性标志物Ki-67标记指数(LI)在内的各种临床病理参数之间的关联。在非癌性肝组织中,EBAG9/RCAS1表达持续处于低水平,呈规则的细胞质分布。在84例HCC肿瘤的表面和细胞质中检测到EBAG9/RCAS1的阳性免疫反应性,染色模式不规则。EBAG9/RCAS1表达增强与较低的分化程度和Ki-67 LI相关。有趣的是,在“结节内结节”肿瘤中,EBAG9/RCAS1表达在分化程度较低的病变中特异性增强。总之,EBAG9/RCAS1与HCC肿瘤去分化和增殖活性增加相关。其确切的功能作用仍有待确定。

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