Wnt配体在恶性黑色素瘤中的表达:初步研究表明与组织病理学特征相关。

K Pham, T Milovanovic, R J Barr, T Truong, R F Holcombe
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引用次数: 55

摘要

目的:分泌的Wnt配体是调节细胞间相互作用和细胞生长分化的关键蛋白。这些蛋白与Wnt信号通路的其他成分一起参与了各种人类癌症的恶性转化,包括恶性黑色素瘤。本研究定义了Wnt配体家族的几个成员的表达,并将其表达与组织学特征联系起来。方法:采用原位、反义RNA杂交法检测良性痣和恶性黑色素瘤石蜡包埋切片中Wnt2、Wnt5a、Wnt5b、Wnt7b和Wnt10b的表达。免疫过氧化物酶抗体染色法测定卷曲(Fz)受体表达。结果:所有naevi检测均强烈表达Wnt2、Wnt5a、Wnt7b和Wnt10b。黑色素瘤的特征是小而均匀的细胞以类似于良性痣的模式表达每种wnt。相反,以大的多形性细胞为特征的黑色素瘤表达Wnt10b,但不表达Wnt2,并且Wnt5a的表达水平较低。Wnt7b在这些黑色素瘤中的表达是可变的。Fz受体在正常上皮和所有痣瘤和黑色素瘤中表达水平较低。结论:Wnt配体在恶性黑色素瘤中的表达模式与组织病理学特征相关,可为该疾病的分子分类提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Wnt ligand expression in malignant melanoma: pilot study indicating correlation with histopathological features.

Aims: Secreted Wnt ligands are key proteins regulating cell-cell interactions and cell growth and differentiation. These proteins, along with other components of the Wnt signalling pathway, are involved in the malignant transformation of various human cancers, including malignant melanoma. This study defines the expression of several members of the Wnt ligand family and correlates their expression with histological characteristics.

Methods: The expression of Wnt2, Wnt5a, Wnt5b, Wnt7b, and Wnt10b was defined by in situ, antisense RNA hybridisation of paraffin wax embedded sections of benign naevi and malignant melanoma. Immunoperoxidase based antibody staining was used to define the expression of frizzled (Fz) receptors.

Results: All naevi tested strongly expressed Wnt2, Wnt5a, Wnt7b, and Wnt10b. Melanomas characterised by small, uniform cells expressed each of the Wnts in a pattern similar to that seen for benign naevi. In contrast, melanomas characterised by large, pleomorphic cells expressed Wnt10b but did not express Wnt2 and had low levels of expression of Wnt5a. Expression of Wnt7b was variable in these melanomas. Fz receptor expression was present at a low level in normal epithelium and all naevi and melanomas.

Conclusions: The expression pattern of Wnt ligands in malignant melanoma correlates with histopathological features and may provide a basis for the molecular classification of this disease.

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