Hussein Mahmoud R
Department of Pathology, Faculty of Medicine, Assuit University, Assuit City, Egypt.
Tumour Biol. 2004 Jul-Aug;25(4):200-7. doi: 10.1159/000081103.
Mutations in the TP53 gene are found in about 11% of melanomas. Although nearly 600 papers have been published with varying degrees of consensus, there does not appear to be any comparable analysis that facilitates more than a glimpse into the role of p53 in melanomagenesis. This article reviews p53 alterations (at the gene and protein levels) in melanocytic skin lesions and discusses the following points: (i) p53 alterations commence as early as at the stage of benign and dysplastic nevi; (ii) these alterations are frequent in melanomas, and gradually increase with their progression; (iii) there is no concordance between the frequent p53 protein expression and the rarity of both TP53 gene mutations in melanomas, and (iv) the entire p53 pathway is a more critical determinant of the fate of the melanocytic skin lesions than the status of the p53 protein or the gene itself.
在约11%的黑色素瘤中发现了TP53基因的突变。尽管已经发表了近600篇论文,且达成了不同程度的共识,但似乎没有任何类似的分析能够让人深入了解p53在黑色素瘤发生中的作用。本文综述了黑素细胞性皮肤病变中p53的改变(基因和蛋白水平),并讨论以下几点:(i)p53改变早在良性和发育异常痣阶段就已开始;(ii)这些改变在黑色素瘤中很常见,并随着肿瘤进展而逐渐增加;(iii)黑色素瘤中p53蛋白表达频繁与TP53基因突变罕见之间不存在一致性;(iv)整个p53信号通路比p53蛋白或基因本身的状态更能决定黑素细胞性皮肤病变的命运。