Wu C L, Roz L, Sloan P, Read A P, Holland S, Porter S, Scully C, Speight P M, Thakker N
Department of Medical Genetics, University of Manchester, United Kingdom.
Genes Chromosomes Cancer. 1997 Dec;20(4):347-53. doi: 10.1002/(sici)1098-2264(199712)20:4<347::aid-gcc5>3.0.co;2-1.
Deletions on chromosome arm 8p, as defined by allelic imbalance, are a frequent event in many different types of malignant tumors, including those of the head and neck. These regions are thought to harbor tumor suppressor genes. In order to define a high-density deletion map of this chromosomal arm in oral and oropharyngeal squamous cell carcinomas, we have tested for allelic imbalance in 35 such tumors with 22 short tandem-repeat polymorphisms. Overall, 21 (60%) of the 35 tumors showed allelic imbalance at one or more loci on chromosome arm 8p. Interstitial deletions defined three discrete areas of deletion: at 8p23, 8p22, and 8p12-p21. Tumors of TNM stages II-IV showed a significantly higher frequency of allelic imbalance on 8p than did TNM stage I tumors. Our data suggest that there are least three tumor suppressor loci on chromosome arm 8p that may be implicated in oral carcinogenesis. Furthermore, inactivation of such genes may be associated with high-grade tumors.
由等位基因不平衡所定义的8号染色体短臂缺失,在包括头颈肿瘤在内的许多不同类型恶性肿瘤中都是常见事件。这些区域被认为含有肿瘤抑制基因。为了确定口腔和口咽鳞状细胞癌中该染色体短臂的高密度缺失图谱,我们用22个短串联重复多态性检测了35例此类肿瘤的等位基因不平衡情况。总体而言,35例肿瘤中有21例(60%)在8号染色体短臂的一个或多个位点表现出等位基因不平衡。间质缺失确定了三个离散的缺失区域:8p23、8p22和8p12-p21。TNM分期为II-IV期的肿瘤在8号染色体短臂上的等位基因不平衡频率显著高于TNM I期肿瘤。我们的数据表明,8号染色体短臂上至少有三个肿瘤抑制位点可能与口腔癌发生有关。此外,此类基因的失活可能与高级别肿瘤有关。