Singh Hariom, Sachan Rekha, Jain Meenu, Mittal Balraj
Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow-226014, India.
Oncol Res. 2008;17(2):87-91. doi: 10.3727/096504008784523667.
Inflammation plays a major role in the pathogenesis of cervical cancer. Chemokines are involved in inflammation, cancer, and infectious diseases. Therefore, we evaluated the association of the chemokine receptor gene polymorphism CCR5 Delta32 with risk of cervical cancer. A total of 150 histopathologically confirmed patients with cervical cancer and 162 age and ethnically matched cervical cytology negative healthy controls were genotyped for CCR5 Delta32 polymorphisms using PCR. Association of CCR5 Delta32 genotypes with risk of cervical cancer, clinical stages, and tobacco exposure was analyzed using chi-square statistical tests. The frequency of the mutant allele CCR5 Delta32 was higher in patients with cervical carcinoma (2.3%) but there was no statistically significant difference (OR = 1.51; p = 0.685;). Association of CCR5 genotypes with clinical phenotypes showed significant risk with stage IB patients due to CCR5+/Delta32 genotype (OR = 4.43; p = 0.021). Furthermore, patients with CCR5+/Delta32 genotype and tobacco usage were at risk of cervical cancer (OR = 1.73, 95% CI = 0.27-1.28). In summary, CCR5 heterozygous genotype (+/Delta32) may significantly influence the early stage of cervical cancer development. However, the cervical cancer risk due to tobacco usage was not significantly modulated after interaction with CCR5+/Delta32 genotype.
炎症在宫颈癌的发病机制中起主要作用。趋化因子参与炎症、癌症和传染病。因此,我们评估了趋化因子受体基因多态性CCR5 Delta32与宫颈癌风险之间的关联。使用聚合酶链反应(PCR)对150例经组织病理学确诊的宫颈癌患者以及162例年龄和种族匹配的宫颈细胞学检查阴性的健康对照者进行CCR5 Delta32多态性基因分型。使用卡方统计检验分析CCR5 Delta32基因型与宫颈癌风险、临床分期和烟草暴露之间的关联。宫颈癌患者中突变等位基因CCR5 Delta32的频率较高(2.3%),但差异无统计学意义(比值比[OR]=1.51;p=0.685)。CCR5基因型与临床表型的关联显示,由于CCR5+/Delta32基因型,IB期患者存在显著风险(OR=4.43;p=0.021)。此外,CCR5+/Delta32基因型且吸烟的患者有患宫颈癌的风险(OR=1.73,95%置信区间[CI]=0.27 - 1.28)。总之,CCR5杂合基因型(+/Delta32)可能显著影响宫颈癌发展的早期阶段。然而,与CCR5+/Delta32基因型相互作用后,吸烟导致的宫颈癌风险没有受到显著调节。