Bhoite L T, Saranath D, Nair R, Deo M G, Sanghavi V, Mehta A
Cell & Developmental Pathology Division, Cancer Research Institute, Parel, Bombay, India.
J Oral Pathol Med. 1993 Aug;22(7):298-302. doi: 10.1111/j.1600-0714.1993.tb01076.x.
Restriction fragment length polymorphism (RFLP) of the human H-ras-1 gene has been indicated as a marker for detection of individuals at high risk of cancer. We have investigated the association of RFLP at the H-ras-1 locus and susceptibility to oral cancer by Southern hybridization analysis in 77 primary oral tumors and 99 healthy donors. The frequency distribution of the BamHI fragments of H-ras-1 revealed homozygous or heterozygous alleles in the two subpopulations. The heterozygous genotype occurred more frequently in the normal subjects (53%) as compared to the cancer patients (36%). Four common alleles-C1 to C4, were noted predominantly in both groups, with rare alleles detected at a lower frequency. The common allele with 7.6 kb BamHI fragment was significantly higher in normals (10%) than in the tumor population (4%) (P < 0.05). However, a similar distribution of rare alleles in both groups indicated that the presence of rare alleles is not indicative of predisposition to oral cancer.
人类H-ras-1基因的限制性片段长度多态性(RFLP)已被指出是检测癌症高危个体的一个标志物。我们通过Southern杂交分析,对77例原发性口腔肿瘤患者和99名健康供体进行了研究,以探讨H-ras-1基因座处的RFLP与口腔癌易感性之间的关联。H-ras-1的BamHI片段的频率分布在两个亚群中显示出纯合或杂合等位基因。与癌症患者(36%)相比,杂合基因型在正常受试者中出现的频率更高(53%)。两组中均主要发现了四个常见等位基因——C1至C4,而罕见等位基因的检出频率较低。具有7.6 kb BamHI片段的常见等位基因在正常人群中的比例(10%)显著高于肿瘤人群(4%)(P < 0.05)。然而,两组中罕见等位基因的分布相似,这表明罕见等位基因的存在并不表明易患口腔癌。