Kalantari M, Karlsen F, Kristensen G, Holm R, Hagmar B, Johansson B
Department of Clinical Virology, Huddinge University Hospital, Sweden.
Int J Gynecol Pathol. 1998 Apr;17(2):146-53. doi: 10.1097/00004347-199804000-00009.
The E1 and E2 reading frames of 158 cervical carcinoma samples containing human papillomavirus (HPV) 16 were mapped using polymerase chain reaction (PCR). The reading frames were amplified using primers spanning the entire genes. Of the analyzed samples, 23% showed no amplification with the E1 primers and 29% showed no amplification with the E2 primers. There was an overlap, but not complete identity, between the E1- and E2-disrupted groups. All E1- and E2-negative samples were further analyzed with primers spanning subsections of the E1 and E2 reading frames, which together covered the entire genes. Of the 35 samples negative for E1, 11 were positive in specific amplification of the 3' end of the E1 gene. Several different subsections of E2 could be amplified from most samples negative for the entire gene (37/46). Five classes of patterns were found, in which either all subsections of the E2 gene or subsections in the 5', middle, or 3' end were disrupted. Although a variable pattern of disruption/deletion in the E1-E2 area of the HPV 16 genome was found in cervical carcinoma, the 5' end disruption was the most common one in both E1 and E2. Patients with carcinomas showing disruptions in E1/E2 had a poorer survival than those without such changes, and E1 disruptions were the most important prognostically.
使用聚合酶链反应(PCR)对158份含有人类乳头瘤病毒16型(HPV - 16)的宫颈癌样本的E1和E2读码框进行定位。使用跨越整个基因的引物扩增读码框。在分析的样本中,23%的样本用E1引物未出现扩增,29%的样本用E2引物未出现扩增。E1和E2破坏组之间存在重叠,但并非完全一致。所有E1和E2阴性的样本进一步用跨越E1和E2读码框各部分的引物进行分析,这些引物共同覆盖了整个基因。在35份E1阴性的样本中,11份在E1基因3'端的特异性扩增中呈阳性。从大多数整个基因阴性的样本(37/46)中可以扩增出E2的几个不同部分。发现了五类模式,其中E2基因的所有部分或5'端、中间或3'端的部分被破坏。尽管在宫颈癌中发现HPV 16基因组E1 - E2区域存在破坏/缺失的可变模式,但5'端破坏在E1和E2中都是最常见的。E1/E2出现破坏的癌症患者的生存率比未发生此类变化的患者低,并且E1破坏在预后方面最为重要。