首页> 外文期刊>Virchows Archiv: an international journal of pathology >KiSS-1 overexpression as an independent prognostic marker in hepatocellular carcinoma: an immunohistochemical study.
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KiSS-1 overexpression as an independent prognostic marker in hepatocellular carcinoma: an immunohistochemical study.

机译:KiSS-1过表达作为肝细胞癌的独立预后标志物:一项免疫组织化学研究。

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摘要

The KiSS-1 gene has been reported to play an important role as a metastasis suppressor gene in various human malignancies. However, there is little information about its possible role in hepatocellular carcinoma (HCC). In this study, we evaluated the prognostic significance of the expression of KiSS-1 and its receptor AXOR12 in 142 HCC tissue specimens by immunohistochemistry. By using a cutoff level of 50%, immunoreactivity of KiSS-1 and AXOR12 was found in 6 (4%) and 11 (8%) HCCs. The expression of KiSS-1 and AXOR12 in HCC correlated with each other (r = 0.42, p < 0.0001) and with the expression in corresponding, surrounding liver tissue (both r = 0.35, p < 0.0001). Positive AXOR12 immunoreactivity in HCC correlated with advanced pT-stage of tumors and low tumor grading (r = 0.18, p = 0.032; r = -0.18, p = 0.029). High KiSS-1 expression in HCC had a statistically significant influence on diminished disease-free and overall survival in uni- (p = 0.006 and p = 0.002) and multivariate analysis (r = 2.874, p = 0.027 and r = 2.913, p = 0.026). In this study, we report for the first time that elevated KiSS-1 expression level in HCC correlates with worsened clinical outcome, as an independent prognostic marker for the aggressiveness of HCC.
机译:据报道,KiSS-1基因在各种人类恶性肿瘤中作为转移抑制基因发挥着重要作用。但是,关于其可能在肝细胞癌(HCC)中的作用的信息很少。在这项研究中,我们通过免疫组织化学评估了KiSS-1及其受体AXOR12在142例HCC组织标本中的表达对预后的意义。通过使用50%的临界水平,在6(4%)和11(8%)HCC中发现KiSS-1和AXOR12的免疫反应性。肝癌中KiSS-1和AXOR12的表达彼此相关(r = 0.42,p <0.0001),并且与周围相应的肝组织中的表达相关(r = 0.35,p <0.0001)。 HCC中阳性AXOR12免疫反应性与晚期pT期肿瘤和低肿瘤分级相关(r = 0.18,p = 0.032; r = -0.18,p = 0.029)。 HCC中高KiSS-1表达对单因素(p = 0.006和p = 0.002)和多因素分析(r = 2.874,p = 0.027和r = 2.913,p = 0.026)。在这项研究中,我们首次报告肝癌中KiSS-1表达水平升高与临床预后恶化相关,这是肝癌侵袭性的独立预后指标。

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