Kamradt J, Reichrath J
Department of Dermatology, Universität des Saarlandes, Hamburg, Germany.
J Histochem Cytochem. 1996 Dec;44(12):1415-20. doi: 10.1177/44.12.8985133.
We analyzed immunohistochemically the expression of RAR proteins in basal cell carcinomas (BCCs; n = 15) in situ. The labeling pattern for the different types of RARs was compared with the staining pattern of the proliferation marker Ki-67 in the same tumors. We found strong immunoreactivity for RAR-alpha and moderate immunoreactivity for RAR-gamma in all BCCs analyzed, whereas no or very weak staining for RAR-beta protein was detected. In contrast to RAR-gamma, which revealed no or only marginal differences in staining intensities, RAR-alpha immunoreactivity was consistently stronger in BCCs compared to adjacent unaffected epidermis. In general, labeling of BCCs for RAR-alpha and RAR-gamma was pronounced in cells of the palisade and peripheral cells, whereas staining in the center of the tumors was heterogeneous. Eleven of the 15 BCCs analyzed revealed no visual correlation in comparing labeling patterns for RAR-alpha and RAR-gamma with the labeling pattern for Ki-67. In four specimens, expression of RAR-alpha, RAR-gamma, and Ki-67 proteins was confined to peripheral tumor cells. Our findings indicate that (a) RAR-alpha and RAR-gamma proteins are, in contrast to RAR-beta, strongly expressed in BCCs; (b) expression of RAR-alpha is upregulated in BCCs compared to keratinocytes of uninvolved epidermis; and (c) BCCs may be targets for potentially preventive or therapeutic treatment with RAR-alpha- or RAR-gamma-selective retinoic acid metabolites.
我们对15例原位基底细胞癌(BCC)进行了RAR蛋白表达的免疫组化分析。将不同类型RAR的标记模式与同一肿瘤中增殖标志物Ki-67的染色模式进行了比较。我们发现,在所有分析的BCC中,RAR-α呈强免疫反应性,RAR-γ呈中度免疫反应性,而未检测到RAR-β蛋白染色或染色非常弱。与RAR-γ染色强度无差异或仅有轻微差异不同,BCC中RAR-α的免疫反应性始终比相邻未受影响的表皮更强。一般来说,BCC中RAR-α和RAR-γ的标记在栅栏状细胞和外周细胞中明显,而肿瘤中心的染色则不均匀。在分析的15例BCC中,有11例在比较RAR-α和RAR-γ的标记模式与Ki-67的标记模式时未发现明显相关性。在4个标本中,RAR-α、RAR-γ和Ki-67蛋白的表达局限于肿瘤外周细胞。我们的研究结果表明:(a)与RAR-β不同,RAR-α和RAR-γ蛋白在BCC中强烈表达;(b)与未受累表皮的角质形成细胞相比,BCC中RAR-α的表达上调;(c)BCC可能是RAR-α或RAR-γ选择性视黄酸代谢物潜在预防或治疗的靶点。