Ohashi A, Funasaka Y, Ueda M, Ichihashi M
Department of Dermatalogy, Kobe University School of Medicine, Japan.
Melanoma Res. 1996 Feb;6(1):25-30. doi: 10.1097/00008390-199602000-00004.
To investigate the role of c-KIT receptor in melanocytic tumour development and progression, we analysed the expression and localization of c-KIT by immunohistochemistry and Western blotting. In contrast to the positive staining shown by melanocytes and naevus cells in the epidermis of common naevi (n=20), all dysplastic naevi (n=13) were negative, as were dermal melanocytic cells of blue naevi (n = 4) and common naevi (n = 26). Three out of four superficial spreading melanomas lost c-KIT expression both in the epidermal and dermal parts, while nodular melanomas showed no expression of c-KIT except in partially positive cells, and six out of seven metastatic melanomas were negative. In acral lentiginous melanomas (n = 8), in contrast to other types of melanoma, all cases with melanoma cells growing basally in the epidermis showed strong c-KIT positivity, but melanoma cells growing at the upper layers of the epidermis and vertically into the dermis lost c-KIT expression. Using the Western blot method on cultured pigment cells, human epidermal melanocytes, junctional naevus cells and one out of three metastatic melanoma cell lines showed 125 and 145 kDa bands corresponding to c-KIT, whereas dermal naevus cells did not. These results suggest that dysplastic naevi are distinct from ordinary naevi in terms of c-KIT expression and that basally growing cells in acral lentigenous melanomas could be at an initial stage of tumour progression, before c-KIT loss occurs.
为了研究c-KIT受体在黑素细胞肿瘤发生和进展中的作用,我们通过免疫组织化学和蛋白质印迹法分析了c-KIT的表达和定位。与普通痣(n = 20)表皮中的黑素细胞和痣细胞呈阳性染色不同,所有发育异常痣(n = 13)均为阴性,蓝色痣(n = 4)和普通痣(n = 26)的真皮黑素细胞也是如此。四分之三的浅表扩散性黑色素瘤在表皮和真皮部分均失去c-KIT表达,而结节性黑色素瘤除部分阳性细胞外未显示c-KIT表达,七分之六的转移性黑色素瘤为阴性。在肢端雀斑样痣性黑色素瘤(n = 8)中,与其他类型的黑色素瘤不同,所有在表皮基底生长的黑色素瘤细胞病例均显示强烈的c-KIT阳性,但在表皮上层生长并垂直进入真皮的黑色素瘤细胞失去c-KIT表达。对培养的色素细胞、人表皮黑素细胞、交界痣细胞和三分之一的转移性黑色素瘤细胞系进行蛋白质印迹分析,结果显示对应于c-KIT的125和145 kDa条带,而真皮痣细胞则未显示。这些结果表明,发育异常痣在c-KIT表达方面与普通痣不同,并且肢端雀斑样痣性黑色素瘤中基底生长的细胞可能处于肿瘤进展的初始阶段,在c-KIT丢失之前。