Peller S, Halperin R, Schneider D, Kopilova Y, Rotter V
Department of Hematology, Assaf-Harofeh Medical Center, Zerifin 70300, Israel.
Oncol Rep. 1999 Jan-Feb;6(1):193-7. doi: 10.3892/or.6.1.193.
The p53 gene is frequently mutated in various human tumors. Polymorphism is an additional genetic alteration observed in exons and introns of the p53 gene of normal tissues and tumors. Distributions of alleles of three common polymorphisms of the p53 gene; a 16 bp duplication in intron 3, codon 72 of exon 4 and a sequence in intron 6, were studied in peripheral white blood cells (WBC) of patients with ovarian or endometrial carcinomas. The analysis was performed by PCR and direct sequencing. The 100% linkage observed between the most common haplotypes of each polymorphism in healthy subjects was lower in the patients. A significant difference was observed between frequencies of genotype and haplotype combinations in patients with ovarian carcinoma and endometrial carcinoma. The incidence of heterozygosity was increased in ovarian carcinoma and decreased in endometrial carcinoma. Our results suggest that the p53 gene may be involved in susceptibility and predisposition to various cancers not only by mutations but also by preferential presentation of polymorphic alleles.
p53基因在多种人类肿瘤中经常发生突变。多态性是在正常组织和肿瘤的p53基因外显子和内含子中观察到的另一种基因改变。研究了p53基因三种常见多态性的等位基因分布,即内含子3中的16bp重复、外显子4的密码子72以及内含子6中的一个序列,这些研究是在卵巢癌或子宫内膜癌患者的外周血白细胞(WBC)中进行的。分析通过PCR和直接测序进行。健康受试者中每种多态性最常见单倍型之间观察到的100%连锁在患者中较低。在卵巢癌和子宫内膜癌患者的基因型和单倍型组合频率之间观察到显著差异。卵巢癌中杂合子发生率增加,而子宫内膜癌中杂合子发生率降低。我们的结果表明,p53基因可能不仅通过突变,而且通过多态性等位基因的优先呈现参与各种癌症的易感性和易患性。