...
首页> 外文期刊>Human Immunology: Official Journal of the American Society for Histocompatibility and Immunogenetics >Genetic polymorphisms of proteasome subunit genes of the MHC-I antigen-presenting system are associated with cervical cancer in a Chinese Han population
【24h】

Genetic polymorphisms of proteasome subunit genes of the MHC-I antigen-presenting system are associated with cervical cancer in a Chinese Han population

机译:MHC-I抗原呈递系统的蛋白酶体亚基基因的遗传多态性与中国汉族人群中的宫颈癌有关

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Proteasome subunit beta types 8 and 9 (PSMB8, PSMB9) play critical roles in the human leukocyte antigen class I (HLA I)-presenting system. Studies have suggested that polymorphisms in the PSMB8 and PSMB9 genes may influence the immune functions of PSMB8 and PSMB9, and thus be associated with various human cancers. We investigated associations involving single nucleotide polymorphisms (SNPs) rs2071543 in PSMB8, rs1351383, rs17587 and rs2127675 in PSMB9 and risk of cervical intraepithelial neoplasia (CIN) and cervical cancer in a Chinese Han population. A total of 543 patients with CIN, 1008 patients with cervical cancer, and 1120 healthy individuals were enrolled. Agena MassArray was used for SNP genotyping of PSMB8 and PSMB9. Associations involving these SNPs and risk of CIN and cervical cancer were analysed. Our results showed that the PSMB8 T/T and T/G genotypes of rs2071543 may be associated with a higher risk of CIN (P = 0.011, OR = 1.35,95% CI: 1.07-1.70) and cervical cancer (P = 0.006, OR = 1.31, 95% CI: 1.08-1.59). For rs17587, the A allele (P = 0.001, OR = 1.303, 95% CI: 1.115-1.522), and the A/A and A/G genotypes (P = 0.001, OR = 1.36, 95% CI: 1.13-1.63) may be risk factors for cervical cancer. These results indicated that PSMB8 rs2071543 might influence susceptibility to CIN and cervical cancer, and PSMB9 rs17587 might influence cervical cancer susceptibility in a Chinese Han population.
机译:蛋白酶体亚单位β8型和9型(PSMB8,PSMB9)在人类白细胞抗原I类(HLA I)呈递系统中起关键作用。研究表明,PSMB8和PSMB9基因的多态性可能会影响PSMB8和PSMB9的免疫功能,从而与各种人类癌症相关。我们调查了中国汉族人群中PSMB8中单核苷酸多态性(SNPs)rs2071543、PSMB9中rs1351383、rs17587和rs2127675与宫颈上皮内瘤变(CIN)和宫颈癌风险的相关性。共有543名CIN患者、1008名宫颈癌患者和1120名健康人入选。Agena MassArray用于PSMB8和PSMB9的SNP基因分型。分析了这些SNP与CIN和宫颈癌风险的相关性。我们的结果显示,rs2071543的PSMB8 T/T和T/G基因型可能与CIN(P=0.011,OR=1.35,95%CI:1.07-1.70)和宫颈癌(P=0.006,OR=1.31,95%CI:1.08-1.59)的较高风险相关。对于rs17587,A等位基因(P=0.001,OR=1.303,95%CI:1.115-1.522)以及A/A和A/G基因型(P=0.001,OR=1.36,95%CI:1.13-1.63)可能是宫颈癌的危险因素。这些结果表明,在中国汉族人群中,PSMB8 rs2071543可能影响CIN和宫颈癌的易感性,而PSMB9 rs17587可能影响宫颈癌易感性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号