Buyru Nur, Altinisik Julide, Isin Mustafa, Dalay Nejat
Department of Medical Biology, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Med Sci Monit. 2008 Sep;14(9):CR493-7.
Several risk factors, both environmental and genetic, have been associated with the pathogenesis of lung cancer. A common polymorphism at codon 72 of exon 4 of the p53 gene encoding either an arginine or proline has been shown to confer susceptibility to the development of different human malignancies. This polymorphism affects proteolytic degradation of p53 promoted by the HPV-E6 protein and represents a risk factor for human-papillomavirus-induced carcinogenesis.
MATERIAL/METHODS: A total of 65 patients with lung cancer were recruited into the study and 87 healthy subjects were used as the control group. The codon 72 polymorphism was determined by the PCR-RFLP method. Presence of human papillomavirus DNA was analyzed by polymerase chain reaction using MY09 and MY11 consensus primers and hybridization with HPV16 and HPV18 specific probes.
The frequencies of the Arg and Pro alleles were 68.46% and 31.54% in lung cancer patients and 55.7% and 44.3% in the healthy control subjects, respectively. These differences were statistically significant. Human papillomavirus DNA was detected in the blood circulation of only 1 patient.
Our results suggest that the Arg/Arg genotype may represent a potential risk factor for the development of lung cancer independent of the HPV infection.
肺癌的发病机制与多种环境和遗传风险因素有关。编码精氨酸或脯氨酸的p53基因第4外显子72密码子处的常见多态性已被证明会使人易患不同的人类恶性肿瘤。这种多态性影响由人乳头瘤病毒E6蛋白促进的p53蛋白水解降解,并且是人类乳头瘤病毒诱导的致癌作用的一个风险因素。
材料/方法:共招募了65例肺癌患者进入本研究,并将87名健康受试者作为对照组。采用PCR-RFLP方法确定72密码子多态性。使用MY09和MY11共有引物通过聚合酶链反应分析人乳头瘤病毒DNA的存在情况,并与HPV16和HPV18特异性探针杂交。
肺癌患者中精氨酸和脯氨酸等位基因的频率分别为68.46%和31.54%,健康对照受试者中分别为55.7%和44.3%。这些差异具有统计学意义。仅在1例患者的血液循环中检测到人乳头瘤病毒DNA。
我们的结果表明,精氨酸/精氨酸基因型可能是独立于HPV感染的肺癌发生的潜在风险因素。