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P-钙黏蛋白、β-连环蛋白以及Wnt5a/卷曲蛋白在黑素细胞肿瘤进展及皮肤黑色素瘤预后中的重要性

Importance of P-cadherin, beta-catenin, and Wnt5a/frizzled for progression of melanocytic tumors and prognosis in cutaneous melanoma.

作者信息

Bachmann Ingeborg M, Straume Oddbjørn, Puntervoll Hanne E, Kalvenes May Britt, Akslen Lars A

机构信息

The Gade Institute, Section for Pathology, University of Bergen, Bergen, Norway.

出版信息

Clin Cancer Res. 2005 Dec 15;11(24 Pt 1):8606-14. doi: 10.1158/1078-0432.CCR-05-0011.

Abstract

PURPOSE

It has been proposed that melanoma cells shift from E-cadherin to N-cadherin expression during tumor development, and recent gene profiling has shown increased expression of Wnt5a/Frizzled in aggressive melanomas possibly by interactions with beta-catenin. We therefore wanted to investigate the role of cadherin subtypes, beta-catenin, and Wnt5a/Frizzled in melanocytic tumors, with focus on prognosis in nodular melanomas.

EXPERIMENTAL DESIGN

The immunohistochemical expression of E-cadherin, N-cadherin, P-cadherin, beta-catenin, and Wnt5a/Frizzled was examined using tissue microarrays of 312 melanocytic tumors.

RESULTS

Cytoplasmic expression of P-cadherin was associated with increasing tumor thickness (P=0.005) and level of invasion (P=0.019), whereas membranous staining was associated with thinner (P=0.012) and more superficial (P=0.018) tumors. Increased cytoplasmic P-cadherin was associated with reduced survival (P=0.047). Lack of nuclear beta-catenin expression was related to increased tumor thickness (P=0.002) and poor patient survival in univariate (P=0.0072) and multivariate (P=0.004) analyses. Membranous expression of N-cadherin was significantly increased from primary tumors to metastatic lesions, whereas E-cadherin staining tended to be decreased. Wnt5a and its receptor Frizzled were highly coexpressed, and nuclear expression of both markers was significantly reduced from benign nevi to melanomas, with a shift from nuclear to cytoplasmic expression in malignant tumors. In addition, Wnt5a expression was significantly associated with nuclear beta-catenin expression.

CONCLUSIONS

Alterations in the expression and subcellular localization of cell adhesion markers are important in the development and progression of melanocytic tumors, and strong cytoplasmic P-cadherin expression and loss of nuclear beta-catenin staining were associated with aggressive melanoma behavior and reduced patient survival.

摘要

目的

有人提出,黑色素瘤细胞在肿瘤发展过程中会从E-钙黏蛋白表达转变为N-钙黏蛋白表达,并且最近的基因谱分析显示,在侵袭性黑色素瘤中Wnt5a/卷曲蛋白(Frizzled)的表达增加,这可能是通过与β-连环蛋白相互作用实现的。因此,我们想研究钙黏蛋白亚型、β-连环蛋白以及Wnt5a/卷曲蛋白在黑素细胞肿瘤中的作用,重点关注结节性黑色素瘤的预后。

实验设计

使用312例黑素细胞肿瘤的组织芯片检测E-钙黏蛋白、N-钙黏蛋白、P-钙黏蛋白、β-连环蛋白以及Wnt5a/卷曲蛋白的免疫组化表达。

结果

P-钙黏蛋白的细胞质表达与肿瘤厚度增加(P=0.005)和侵袭水平增加(P=0.019)相关,而膜染色与较薄(P=0.012)和更表浅(P=0.018)的肿瘤相关。细胞质P-钙黏蛋白增加与生存率降低相关(P=0.047)。在单因素(P=0.0072)和多因素(P=0.004)分析中,缺乏核β-连环蛋白表达与肿瘤厚度增加(P=0.002)和患者生存率低相关。从原发性肿瘤到转移性病变,N-钙黏蛋白的膜表达显著增加,而E-钙黏蛋白染色趋于减少。Wnt5a及其受体卷曲蛋白高度共表达,从良性痣到黑色素瘤,这两种标志物的核表达均显著降低,在恶性肿瘤中表达从核内转移至细胞质。此外,Wnt5a表达与核β-连环蛋白表达显著相关。

结论

细胞黏附标志物的表达和亚细胞定位改变在黑素细胞肿瘤的发生和发展中很重要,强烈的细胞质P-钙黏蛋白表达和核β-连环蛋白染色缺失与侵袭性黑色素瘤行为及患者生存率降低相关。

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