Storey A, Thomas M, Kalita A, Harwood C, Gardiol D, Mantovani F, Breuer J, Leigh I M, Matlashewski G, Banks L
Imperial Cancer Research Fund, Skin Tumour Laboratory, London, UK.
Nature. 1998 May 21;393(6682):229-34. doi: 10.1038/30400.
The E6 oncoprotein derived from tumour-associated human papillomaviruses (HPVs) binds to and induces the degradation of the cellular tumour-suppressor protein p53. A common polymorphism that occurs in the p53 amino-acid sequence results in the presence of either a proline or an arginine at position 72. The effect of this polymorphism on the susceptibility of p53 to E6-mediated degradation has been investigated and the arginine form of p53 was found to be significantly more susceptible than the proline form. Moreover, allelic analysis of patients with HPV-associated tumours revealed a striking overrepresentation of homozygous arginine-72 p53 compared with the normal population, which indicated that individuals homozygous for arginine 72 are about seven times more susceptible to HPV-associated tumorigenesis than heterozygotes. The arginine-encoding allele therefore represents a significant risk factor in the development of HPV-associated cancers.
源自肿瘤相关人乳头瘤病毒(HPV)的E6癌蛋白与细胞肿瘤抑制蛋白p53结合并诱导其降解。p53氨基酸序列中出现的一种常见多态性导致第72位存在脯氨酸或精氨酸。已经研究了这种多态性对p53对E6介导降解的敏感性的影响,发现p53的精氨酸形式比脯氨酸形式明显更易受影响。此外,对HPV相关肿瘤患者的等位基因分析显示,与正常人群相比,纯合精氨酸72 p53明显过多,这表明精氨酸72纯合个体比杂合子患HPV相关肿瘤的易感性高约7倍。因此,编码精氨酸的等位基因是HPV相关癌症发生的一个重要危险因素。