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皮肤黑素细胞肿瘤中埃兹蛋白和CD44的表达

Moesin and CD44 expression in cutaneous melanocytic tumours.

作者信息

Ichikawa T, Masumoto J, Kaneko M, Saida T, Sagara J, Taniguchi S

机构信息

Department of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

Br J Dermatol. 1998 May;138(5):763-8. doi: 10.1046/j.1365-2133.1998.02255.x.

Abstract

The ERM (ezrin, radixin and moesin) family members, located just beneath the plasma membranes, are thought to be involved in the association of action filaments with the plasma membrane. One of the family members, moesin, is reported to bind to CD44. Splice variants of CD44 are thought to be associated with tumour progression or differentiation. Our aim was to investigate immunohistochemically the expression of moesin together with CD44 on paraffin tissue sections of a series of melanocytic tumours. The material included 12 ordinary melanocytic naevi, six Spitz naevi, eight dysplastic naevi, six blue naevi, seven malignant melanomas in situ, 15 primary malignant melanomas, five metastatic melanomas to the skin and five lymph node metastases. In the normal skin and the melanocytic tumours the expression of moesin was largely similar to that of CD44 standard. Strong moesin staining was observed in benign melanocytic lesions and melanomas in situ. However, the expression was decreased in advanced malignant melanomas. The moesin labelling in melanoma cells was downregulated with the depth of dermal invasion. The immunoreactivity was also diminished in the skin metastases and the lymph node metastases of melanoma. These results suggest that in melanocytic tumours, the alternation in the expression of moesin may be involved in the progression of malignancy.

摘要

埃兹蛋白、根蛋白和膜突蛋白(ERM)家族成员位于质膜下方,被认为参与了肌动蛋白丝与质膜的结合。据报道,该家族成员之一膜突蛋白可与CD44结合。CD44的剪接变体被认为与肿瘤进展或分化有关。我们的目的是通过免疫组织化学方法研究一系列黑素细胞肿瘤石蜡组织切片中膜突蛋白与CD44的表达情况。材料包括12例普通黑素细胞痣、6例Spitz痣、8例发育异常痣、6例蓝痣、7例原位恶性黑色素瘤、15例原发性恶性黑色素瘤、5例皮肤转移性黑色素瘤和5例淋巴结转移瘤。在正常皮肤和黑素细胞肿瘤中,膜突蛋白的表达与CD44标准型的表达基本相似。在良性黑素细胞病变和原位黑色素瘤中观察到强膜突蛋白染色。然而,在晚期恶性黑色素瘤中表达降低。黑色素瘤细胞中的膜突蛋白标记随着真皮浸润深度而下调。在黑色素瘤的皮肤转移灶和淋巴结转移灶中免疫反应性也降低。这些结果表明,在黑素细胞肿瘤中,膜突蛋白表达的改变可能参与了恶性进展。

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