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在中国女性中,部分而非全部HLA-II等位基因与宫颈癌相关。

Some but not all of HLA-II alleles are associated with cervical cancer in Chinese women.

作者信息

Liang Jinxiao, Xu Anlong, Xie Yufen, Awonuga Awoniyi O, Lin Zhongqiu

机构信息

Second Affiliated Hospital, Sun Yatsen University, 107 Yan Jiang West Road, Guangzhou, 510120, P.R. China.

出版信息

Cancer Genet Cytogenet. 2008 Dec;187(2):95-100. doi: 10.1016/j.cancergencyto.2008.07.011.

Abstract

Cervical cancer (CC) is closely associated with the human papillomavirus (HPV). Although most patients are able to clear the infection over time, some eventually develop cancer, suggesting the existence of other factors that determine malignant progression. Such factors may include genetic susceptibility. To determine whether human leukocyte antigen (HLA) class II is related to CC among Han race population in the Guangdong region of China, HLA class II typing were carried out by polymerase chain reaction in 126 patients with CC and 88 selected controls. The allele and haplotype frequencies in both the study and control groups were calculated. The occurrence of DPB1 *1301 [odds ratio (OR), 2.66; 95% confidence interval (CI), 1.12-6.29], DPB1 *0202 (OR, 3.65; CI, 1.04-12.80), DQB1 *030302(OR, 1.85; CI, 1.04-3.27), and DQB1 *050301(OR, 3.94; CI, 1.48-10.46) alleles were more common in the study group than control. This suggests that these alleles may confer susceptibility to CC in the Guangdong Province. In a similar fashion, the occurrence of DRB1 *13-DQB1 *06 (OR, 0.17; 95% CI, 0.04-0.80) haplotype was significantly lower in the study patients compared with the controls and may confer a decreased risk of CC among Han race population in the Guangdong Province of China.

摘要

宫颈癌(CC)与人乳头瘤病毒(HPV)密切相关。尽管大多数患者能够随着时间的推移清除感染,但有些患者最终会发展为癌症,这表明存在其他决定恶性进展的因素。这些因素可能包括遗传易感性。为了确定中国广东地区汉族人群中人类白细胞抗原(HLA)II类是否与CC相关,对126例CC患者和88例选定的对照进行了聚合酶链反应HLA II类分型。计算了研究组和对照组的等位基因和单倍型频率。研究组中DPB1 *1301[比值比(OR),2.66;95%置信区间(CI),1.12 - 6.29]、DPB1 *0202(OR,3.65;CI,1.04 - 12.80)、DQB1 *030302(OR,1.85;CI,1.04 - 3.27)和DQB1 *050301(OR,3.94;CI,1.48 - 10.46)等位基因的出现频率高于对照组。这表明这些等位基因可能使广东省人群易患CC。同样,与对照组相比,研究组患者中DRB1 *13 - DQB1 *06单倍型(OR,0.17;95%CI,0.04 - 0.80)的出现频率显著较低,并且可能使中国广东省汉族人群患CC的风险降低。

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