Ishwad C S, Ferrell R E, Rossie K N, Appel B N, Johnson J T, Myers E N, Law J C, Srivastava S, Gollin S M
Department of Human Genetics, University of Pittsburgh, PA, USA.
Int J Cancer. 1996 Feb 20;69(1):1-4. doi: 10.1002/(SICI)1097-0215(19960220)69:1<1::AID-IJC1>3.0.CO;2-8.
Loss of heterozygosity (LOH) on chromosomes 3p and 9p has been documented in a variety of malignancies, which suggests the presence of tumor suppressor gene loci on these chromosomes. We have studied 77 oral carcinomas for LOH using 16 microsatellite markers distributed over 5 human chromosomes. Fifty-five (71%) of these tumors showed LOH at one or more loci. A significant proportion of LOH at the informative tumors was observed at chromosomes 3p and 9p: 58% and 48%, respectively. A majority of the tumors showed losses at multiple loci on chromosomes 3p or 9p or on both. Our results suggest that tumor suppressor genes located on the short arms of chromosomes 3 and 9 may be involved in the pathogenesis of oral carcinoma. These regions of deletion observed in oral cancers overlap those reported in other neoplasms. However, we did not find any evidence of these changes in tumor margins with early pathological changes.
3号染色体短臂(3p)和9号染色体短臂(9p)的杂合性缺失(LOH)已在多种恶性肿瘤中得到证实,这表明这些染色体上存在肿瘤抑制基因位点。我们使用分布在5条人类染色体上的16个微卫星标记,对77例口腔癌进行了LOH研究。其中55例(71%)肿瘤在一个或多个位点显示出LOH。在信息性肿瘤中,3p和9p染色体上观察到相当比例的LOH,分别为58%和48%。大多数肿瘤在3p或9p染色体或两者的多个位点出现缺失。我们的结果表明,位于3号和9号染色体短臂上的肿瘤抑制基因可能参与口腔癌的发病机制。在口腔癌中观察到的这些缺失区域与其他肿瘤中报道的区域重叠。然而,我们在早期病理变化的肿瘤边缘未发现这些变化的任何证据。