Jafari M, Papp T, Kirchner S, Diener U, Henschler D, Burg G, Schiffmann D
Institute of Pharmacology and Toxicology, University of Würzburg, Germany.
J Cancer Res Clin Oncol. 1995;121(1):23-30. doi: 10.1007/BF01202725.
We have analyzed the Ha-ras, Ki-ras and N-ras gene for point mutations at codons 12, 13 and 61 via restriction fragment length polymorphism/polymerase chain reaction analysis and subsequent direct sequencing in non-cultured fresh-frozen tissues of 16 superficial spreading melanomas (SSM), 13 nodular malignant melanomas (NMM), 2 lentigo malignant melanomas (LMM), 1 dysplastic nevus, 1 congenital nevus and 5 normal nevi from 38 patients. Mutations were found in 4 melanoma samples, all belonging to the nodular malignant type. Three of them were mutated in N-ras and one in the Ha-ras gene. Mutation in N-ras was also detected in the congenital nevus. All mutations were exclusively located at the first two base pairs of codon 61. No Ki-ras mutation was detected in any lesion. No mutation could be found in SSM and LMM in addition to dysplastic and normal nevi. The frequency of ras mutation in NMM was 31%, whereas in SSM it was 0%. Our study suggests (a) an association between ras mutations (mainly N-ras) and the NMM as a subgroup of human melanoma; (b) that activation of Ki-ras is not involved in the pathogenesis of melanoma. The role of UV radiation in point mutations of ras genes in human melanoma is discussed.
我们通过限制性片段长度多态性/聚合酶链反应分析及随后的直接测序,对38例患者的16例浅表扩散性黑色素瘤(SSM)、13例结节性恶性黑色素瘤(NMM)、2例雀斑样恶性黑色素瘤(LMM)、1例发育异常痣、1例先天性痣和5例正常痣的非培养新鲜冷冻组织中Ha-ras、Ki-ras和N-ras基因密码子12、13和61处的点突变进行了分析。在4例黑色素瘤样本中发现了突变,均属于结节性恶性类型。其中3例N-ras基因发生突变,1例Ha-ras基因发生突变。在先天性痣中也检测到N-ras基因突变。所有突变均仅位于密码子61的前两个碱基对处。在任何病变中均未检测到Ki-ras基因突变。除发育异常痣和正常痣外,在SSM和LMM中未发现突变。NMM中ras基因突变的频率为31%,而SSM中为0%。我们的研究表明:(a)ras基因突变(主要是N-ras)与作为人类黑色素瘤一个亚组的NMM之间存在关联;(b)Ki-ras的激活不参与黑色素瘤的发病机制。本文还讨论了紫外线辐射在人类黑色素瘤ras基因点突变中的作用。