Clinicopathological significance of missing in metastasis B expression in hepatocellular carcinoma

被引:66
|
作者
Ma, Stephanie
Guan, Xin-Yuan
Lee, Terence K.
Chan, Kwok Wah [1 ]
机构
[1] Univ Hong Kong, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Dept Surg, Hong Kong, Hong Kong, Peoples R China
关键词
hepatocellular carcinoma; MIM-B; real-time quantitative PC;
D O I
10.1016/j.humpath.2007.01.004
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Missing in metastasis (MIM) proteins are important regulators in controlling cell growth and development. There has been accumulating evidence suggesting a role of MIM-B in carcinogenesis, yet its role in the development of hepatocellular carcinoma has not been examined thus far. In this study, we investigated the clinicopathological significance of MIM-B in tumor and its matched adjacent nontumor tissue obtained from 40 patients with hepatocellular carcinoma. Increased MIM-B messenger RNA and protein expression, as detected by quantitative real-time polymerase chain reaction and Western blot, respectively, was found in hepatocellular carcinoma clinical samples; and its expression was significantly associated with early pathologic tumor-node-metastasis stage group (P = .007), presence of tumor encapsulation (P = .034), and absence of venous infiltration (P = .038). Higher levels of MIM-B expression were found to be associated with early stage disease. Elevated MIM-B expression may influence the development of hepatocellular carcinoma and may possibly be a powerful indicator for the disease at an early stage. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1201 / 1206
页数:6
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