Hadhri-Guiga Boutheina, Khabir Abdel-Majid, Mokdad-Gargouri Raja, Ghorbel Abdel-Monem, Drira Mohamed, Daoud Jamel, Frikha Mounir, Jlidi Rachid, Gargouri Ali
Laboratoire de Génétique Moléculaire des Eucaryotes, Centre de Biotechnologie de Sfax, BP K 3038 Sfax, Tunisia.
Virus Res. 2006 Jan;115(1):24-30. doi: 10.1016/j.virusres.2005.07.002. Epub 2005 Sep 8.
Nasopharyngeal carcinoma (NPC) occurs with a striking geographic distribution, it is endemic in certain areas of Southeast Asia and North Africa. NPC is tightly linked to Epstein-Barr virus (EBV), however, only a small subset of EBV genes are expressed, among them the latent membrane protein 1 (LMP1). LMP1 is considered as the main EBV oncoprotein and its 30 bp deleted-variant has been reported to be more prevalent in biopsies of NPC. We have assessed the 30 bp deletion and the XhoI polymorphisms of the BNLF1 gene in 30 peripheral bloods of NPC patients and 62 nasopharyngeal biopsies, 42 being confirmed as undifferentiated nasopharyngeal carcinoma and 20 are normal nasopharyngeal epithelium cells. Our results show that 100% of individuals retained the XhoI restriction site. A rare NPC variant, having a 69 bp deletion in the C-terminus region of the BNLF1 gene, covering the 30 bp deletion, was found in two NPC biopsies. The deleted 30 and 69 bp deleted-variants are significantly (p = 0.006) more frequent in NPC (71.42%) than in control biopsies (52%). In peripheral blood of NPC patients, the deleted-variants (47%) are also lower than in tumor tissues (p = 0.0004), suggesting that the deletion could be associated with a risk of tumor genesis. Direct repeats, located at the extremities of the 30 and 69 bp deletions, should be involved in this process. We propose that other deletions could be found since another similar direct repeat is present at the vicinity of the former ones.
鼻咽癌(NPC)的发生具有显著的地理分布特征,在东南亚和北非的某些地区呈地方性流行。鼻咽癌与爱泼斯坦-巴尔病毒(EBV)紧密相关,然而,EBV只有一小部分基因表达,其中包括潜伏膜蛋白1(LMP1)。LMP1被认为是主要的EBV癌蛋白,据报道其30bp缺失变体在鼻咽癌活检中更为普遍。我们评估了30例鼻咽癌患者外周血和62份鼻咽活检组织中BNLF1基因的30bp缺失和XhoI多态性,其中42份被确诊为未分化鼻咽癌,20份为正常鼻咽上皮细胞。我们的结果显示,100%的个体保留了XhoI酶切位点。在两份鼻咽癌活检组织中发现了一种罕见的鼻咽癌变体,其BNLF1基因C末端区域有69bp缺失,涵盖了30bp缺失。缺失的30bp和69bp变体在鼻咽癌(71.42%)中比在对照活检组织(52%)中显著更频繁(p = 0.006)。在鼻咽癌患者的外周血中,缺失变体(47%)也低于肿瘤组织(p = 0.0004),这表明该缺失可能与肿瘤发生风险相关。位于30bp和69bp缺失末端的直接重复序列可能参与了这一过程。我们推测,由于在前述序列附近存在另一个类似的直接重复序列,可能会发现其他缺失情况。