Southern S A, Evans M F, Herrington C S
Department of Pathology, University of Liverpool, Royal Liverpool University Hospital, United Kingdom.
Cancer Res. 1997 Oct 1;57(19):4210-3.
We have analyzed 60 low-grade cervical squamous intraepithelial lesions for low- and high-risk human papillomaviruses (HPVs) and for numerical abnormalities of chromosomes 1, 3, 11, 17, and 18 and the X chromosome. Eleven of 33 lesions infected with high-risk HPVs (HPV 16, 18, 30, 31, 33, 35, 39, 45, 51, 52, 56, 58, and 66) but none of 24 lesions infected with low-risk HPVs (HPV 6, 11, 42, 43, and 44) and none of 15 normal cervices showed basal cell tetrasomy of all six chromosomes in the HPV-infected areas. These changes were not HPV type specific and were not present in all lesions infected with the same HPV type. The presence of basal cell tetrasomy in lesions infected with high- but not low-risk HPVs suggests that induction of chromosome instability may be one mechanism underlying the biological differences between these viral types.
我们分析了60例低级别宫颈鳞状上皮内病变,检测其低风险和高风险人乳头瘤病毒(HPV)以及1号、3号、11号、17号、18号染色体和X染色体的数目异常情况。33例感染高风险HPV(HPV 16、18、30、31、33、35、39、45、51、52、56、58和66)的病变中有11例出现异常,但24例感染低风险HPV(HPV 6、11、42、43和44)的病变以及15例正常宫颈在HPV感染区域均未出现所有6条染色体的基底细胞四体性。这些变化并非HPV型别特异性的,且并非在所有感染相同HPV型别的病变中都存在。高风险而非低风险HPV感染的病变中出现基底细胞四体性,这表明诱导染色体不稳定可能是这些病毒型别之间生物学差异的一种潜在机制。