目的:探讨HLA-B等位基因多态性与新疆地区鼻咽癌的关系及其临床意义。方法纳入226例患者作为鼻咽癌组,207例健康志愿者作为健康对照组。采用PCR-SSP法对HLA-B等位基因进行检测。采用χ2检验两组之间、汉族和维吾尔族之间、鼻咽癌不同临床特征之间HLA-B等位基因频率差异。 Kaplan-Meier 法计算生存率并 Logrank 单因素分析与 HLA-B 等位基因频率关系。结果鼻咽癌组HLA-B*46等位基因频率高于健康对照组( P=0.000),且HLA-B*46等位基因频率在汉族存在差异性(P=0.000),而维吾尔族未发现差异性(P>0.05)。<30岁组HLA-B*44等位基因频率高于≥30岁组( P=0.029);分化型非角化性癌和T1+T2期HLA-B*48等位基因频率分别高于未分化型非角化性癌和T3+T4期( P=0.029)。鼻咽癌5年OS、DFS、DMFS、LRFS率与HLA-B*46(P=0.118~0.502)、HLA-B*44(P=0.761~0.804)及HLA-B*48(P=0.308~0.727)表达状态无关。结论 HLA-B*46等位基因可能为新疆地区汉族鼻咽癌的易感基因,而HLA-B*44可能与较早发病年龄有关,HLA-B*48可能与病理类型及T分期有关。故HLA-B等位基因可能与鼻咽癌发生、发展有关。
Objective To explore the relationship between HLA-B allele polymorphisms and nasopharyngeal carcinoma ( NPC) in Xinjiang, China and its clinical significance. Methods A total of 226 patients were assigned to NPC group, while 207 healthy volunteers were assigned to control group. PCR amplification with sequence-specific primers was used to determine HLA-B alleles. Comparison of HLA-B allele frequency between the above two groups, between Han and Uygur populations, and between patients with various clinical characteristics of NPC was made by chi-square test. The Kaplan-Meier method was used to calculate the survival rates and the log-rank univariate analysis was used to explore the relationship between survival rates and HLA-B allele frequency. Results In all the subjects or Han population alone, the allele frequency of HLA-B*46 in the NPC group was significantly higher than that in the control group ( P=0. 000;P=0. 000 ) . In Uygur population, however, there was no significant difference in the allele frequency of HLA-B*46 between the NPC group and the control group (P〉0. 05). In the patients with NPC, those less than 30 years old had a significantly higher allele frequency of HLA-B*44 than those no less than 30 years old (P=0. 029);those with differentiated non-keratinizing carcinoma had a significantly higher allele frequency of HLA-B*48 than those with undifferentiated non-keratinizing carcinoma ( P=0. 029);those with stage T1+T2 disease had a significantly higher allele frequency of HLA-B*48 than those with stage T3+T4 disease ( P=0. 029) . The 5-year overall survival, disease-free survival, distant metastasis-free survival, and local relapse-free survival rates had no relationship with the expression of HLA-B*46, HLA-B*44, or HLA-B*48 in NPC patients ( all P〉0. 05) . Conclusions HLA-B*46 allele is probably a NPC susceptibility gene in Han population in Xinjiang. HLA-B*44 is probably associated with early age of onset, while HLA-B*48 is probably associa