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LAPTM4B-35 是肝癌的一个新的预后因素。

LAPTM4B-35 is a novel prognostic factor of hepatocellular carcinoma.

机构信息

Department of Cell Biology, School of Basic Medical Sciences, Peking University, Beijing, China.

出版信息

J Surg Oncol. 2010 Apr 1;101(5):363-9. doi: 10.1002/jso.21489.

Abstract

BACKGROUND

LAPTM4B-35 is a 35-kDa tetra-transmembrane protein overexpressed in hepatocellular carcinoma (HCC) and promotes cell survival, proliferation, and tumorigenesis. However, the potential clinical implications of LAPTM4B-35 in HCC are still unclear. This study is aimed to investigate the correlations between LAPTM4B-35 expression and prognosis in patients with HCC.

METHODS

Western blot and immunohistochemistry assays were used to determine the expression of LAPTM4B-35 in HCCs and their paired noncancerous liver tissues from 65 patients. The correlations of LAPTM4B-35 expression with clinicopathological parameters were assessed by Chi-square test. Patient survival was determined by Kaplan-Meier method and log-rank test. Cox regression was adopted for multivariate analysis of prognostic factors.

RESULTS

LAPTM4B-35 overexpression occurred in 76.9% of HCC tissues, while only in 4.6% of noncancerous liver tissues. Overexpression of LAPTM4B-35 was significantly associated with TNM staging and invasive tumors. Patients with higher LAPTM4B-35 expression had significantly poorer overall survival (OS) and disease-free survival (DFS) (both P < 0.001). On multivariate analysis, elevated expression of LAPTM4B-35 was found to be an independent prognostic factor for OS and DFS (P = 0.009, 0.043, respectively).

CONCLUSIONS

LAPTM4B-35 overexpression is an independent prognostic factor for OS and DFS of HCC.

摘要

背景

LAPTM4B-35 是一种在肝细胞癌(HCC)中过度表达的 35kDa 四跨膜蛋白,可促进细胞存活、增殖和肿瘤发生。然而,LAPTM4B-35 在 HCC 中的潜在临床意义尚不清楚。本研究旨在探讨 LAPTM4B-35 表达与 HCC 患者预后的相关性。

方法

使用 Western blot 和免疫组织化学检测 65 例 HCC 及其配对的非癌性肝组织中 LAPTM4B-35 的表达。通过卡方检验评估 LAPTM4B-35 表达与临床病理参数的相关性。采用 Kaplan-Meier 法和对数秩检验确定患者的生存情况。采用 Cox 回归进行预后因素的多因素分析。

结果

LAPTM4B-35 的过表达发生在 76.9%的 HCC 组织中,而仅在 4.6%的非癌性肝组织中发生。LAPTM4B-35 的过表达与 TNM 分期和侵袭性肿瘤显著相关。LAPTM4B-35 表达较高的患者总生存期(OS)和无病生存期(DFS)明显较差(均 P<0.001)。多因素分析显示,LAPTM4B-35 的高表达是 OS 和 DFS 的独立预后因素(P=0.009、0.043)。

结论

LAPTM4B-35 的过表达是 HCC OS 和 DFS 的独立预后因素。

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