Busby-Earle R M, Steel C M, Bird C C
Department of Pathology, Edinburgh University Medical School, UK.
Br J Cancer. 1993 Jan;67(1):71-5. doi: 10.1038/bjc.1993.11.
Twenty cervical carcinomas were examined for loss of heterozygosity (LOH) using 22 RFLP markers, which mapped to regions of putative oncosuppressor gene loci, identified as candidates in other common solid tumours. Allele losses were identified in six of the eight chromosomal arms examined, but at a significantly lower frequency than that reported in other common solid tumours. No association was observed between allele losses at any chromosomal location and the presence or integration of 'high risk' types of HPV determined by a sensitive, specific PCR method. HPV 16, 18 or 33 were found in the majority (75%) of these tumours. We have looked at only a limited subset of chromosomal regions, but the results, so far, imply that carcinoma of the cervix may arise by different molecular events than other common solid tumours, and support the view that one of the distinctive events may be infection with HPV. Alternatively, similar molecular events may be occurring, but in regions of the genome not yet identified as targets in other solid tumours.
使用22个RFLP标记对20例宫颈癌进行杂合性缺失(LOH)检测,这些标记定位于假定的肿瘤抑制基因位点区域,这些区域在其他常见实体瘤中被确定为候选区域。在所检测的8个染色体臂中的6个中发现了等位基因缺失,但频率明显低于其他常见实体瘤中的报道。通过敏感、特异的PCR方法确定,在任何染色体位置的等位基因缺失与“高危”型HPV的存在或整合之间均未观察到关联。在这些肿瘤的大多数(75%)中发现了HPV 16、18或33。我们仅研究了染色体区域的一个有限子集,但目前的结果表明,宫颈癌的发生可能是由与其他常见实体瘤不同的分子事件引起的,并支持这样一种观点,即其中一个独特事件可能是HPV感染。或者,可能正在发生类似的分子事件,但发生在基因组中尚未被确定为其他实体瘤靶点的区域。