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突尼斯女性中HLA-II类基因对宫颈癌的易感性

HLA class II susceptibility to cervical cancer among Tunisian women.

作者信息

Ben Othmane Yosra, Ghazouani Ezzeddine, Mezlini Amel, Lagha Awatef, Raïs Mejda, Kochkar Radhia, Zidi Sabrina, Afrit Mehdi, Mota-Vieira Luisa, Yacoubi Loueslati Besma

机构信息

El Manar University, Laboratory of Micro-Organisms and Active Biomolecules, Tunis, Tunisia.

出版信息

Bull Cancer. 2012 Sep;99(9):81-6. doi: 10.1684/bdc.2012.1623.

Abstract

The variability in host immunogenetic background, especially in human major histocompatibilty genes, has been shown to influence the susceptibility to human papillomavirus (HPV) infection and cervical neoplasia. Here, we conducted a case-control study in Tunisian women to examine the effect of genetic variation in HLA class II DRB1 and DQB1 genes on invasive cervical cancer (ICC) and squamous cell carcinoma (SCC). HLA genotyping was performed by PCR sequence-specific primers technique. The data revealed significant positive and negative associations, suggesting either predisposing or protective effects of these genes in the disease outcome. DRB115, alone or linked to DQB106, was associated with a 2.7- and 3.5-fold increase in risk for ICC, respectively. DRB113-DQB103 showed a similar 3.5 risk effect. Concerning SCC, we observed a relatively higher, about 1.2 times more, risk effect for these genetic markers. In contrast, only one haplotype - DRB113-DQB106 - provides evidence for a weak protection (about 0.3-fold reduction) of ICC and SCC. In conclusion, we suggest that HLA class II polymorphisms are involved in the genetic susceptibility to cervical cancer in Tunisian women.

摘要

宿主免疫遗传背景的变异性,尤其是人类主要组织相容性基因的变异性,已被证明会影响人乳头瘤病毒(HPV)感染及宫颈肿瘤形成的易感性。在此,我们对突尼斯女性进行了一项病例对照研究,以检验HLA II类DRB1和DQB1基因的遗传变异对浸润性宫颈癌(ICC)和鳞状细胞癌(SCC)的影响。通过聚合酶链反应序列特异性引物技术进行HLA基因分型。数据显示出显著的正相关和负相关,表明这些基因在疾病转归中具有易感性或保护性作用。单独的DRB115或与DQB106连锁时,分别与ICC风险增加2.7倍和3.5倍相关。DRB113-DQB103显示出相似的3.5倍风险效应。关于SCC,我们观察到这些遗传标记具有相对较高的风险效应,约为1.2倍。相比之下,只有一种单倍型——DRB113-DQB106——为ICC和SCC提供了弱保护(约降低0.3倍)的证据。总之,我们认为HLA II类多态性参与了突尼斯女性宫颈癌的遗传易感性。

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