Wright K, Wilson P J, Kerr J, Do K, Hurst T, Khoo S K, Ward B, Chenevix-Trench G
Queensland Cancer Research Unit, The Queensland Institute of Medical Research, Herston, Brisbane, Australia.
Oncogene. 1998 Sep 3;17(9):1185-8. doi: 10.1038/sj.onc.1202028.
Many chromosomal regions undergo loss of heterozygosity (LOH) in ovarian adenocarcinomas but few of the target regions have been finely mapped. One of the chromosome arms likely to harbour one or more tumour suppressor genes inactivated in ovarian cancer is the short arm of chromosome 8 which is frequently deleted in many other solid tumours. We have examined a large panel of microsatellite markers on 8p for LOH in 53 ovarian adenocarcinomas. LOH was observed in 27 tumours (51%), with a significant trend towards a higher frequency of LOH in more advanced tumours. Detailed examination of nine tumours with partial deletions defined three regions of overlap, two in 8p23 and one in 8p22, which suggests that there might be as many as three tumour or metastasis suppressor genes on 8p which are inactivated during ovarian tumorigenesis. LOH on 8p was significantly associated with 9p LOH which suggests that inactivation of target genes on these chromosomes may be cooperative events.
许多染色体区域在卵巢腺癌中会发生杂合性缺失(LOH),但很少有目标区域被精细定位。8号染色体短臂很可能含有一个或多个在卵巢癌中失活的肿瘤抑制基因,该短臂在许多其他实体瘤中也经常发生缺失。我们检测了53例卵巢腺癌中8号染色体短臂上大量微卫星标记的杂合性缺失情况。在27例肿瘤(51%)中观察到杂合性缺失,且在进展期肿瘤中杂合性缺失频率呈显著升高趋势。对9例部分缺失肿瘤的详细检查确定了三个重叠区域,两个在8p23,一个在8p22,这表明8号染色体短臂上可能有多达三个肿瘤或转移抑制基因在卵巢肿瘤发生过程中失活。8号染色体短臂上的杂合性缺失与9号染色体短臂上的杂合性缺失显著相关,这表明这些染色体上目标基因的失活可能是协同事件。