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鼻咽癌中3p21.3处乳铁传递蛋白的遗传和表观遗传改变。

Genetic and epigenetic alterations of LTF at 3p21.3 in nasopharyngeal carcinoma.

作者信息

Yi Hong-Mei, Li Hui, Peng Dan, Zhang He-Jun, Wang Lei, Zhao Ming, Yao Kai-Tai, Ren Cai-Ping

机构信息

Cancer Research Institute, Xiang-Ya School of Medicine, Central South University, Changsha, Hunan, P. R. China.

出版信息

Oncol Res. 2006;16(6):261-72. doi: 10.3727/000000006783981008.

Abstract

To investigate the roles of lactotransferrin gene (LTF, also referred to as the lactoferrin gene, LF), located at 3p21.3 within the common minimal deletion region, in the pathogenesis of nasopharyngeal carcinoma (NPC), we first detected its expression level in 33 primary NPC tissues and 15 chronic nasopharyngitis tissues. Absent expression or downregulation of LTF were observed in 76% (25 of 33) of primary NPC tissues. We further found that 25% (5 of 20) of NPC specimens had loss of heterozygosity (LOH) at the LTF locus. LTF mutation assessed by polymerase chain reaction single-strand conformation polymorphism (PCR-SSCP) and DNA sequencing was noted in 30% (6 of 20) of primary NPC tissues. In addition, hyper-methylation of LTF promoter region was found in 63.6% (21 of 33) of primary NPC samples but not in chronic nasopharyngitis tissues. The LTF transcripts in NPC cell lines increased upon treatment with the demethylation compound, 5-aza-2-deoxycytidine. In conclusion, our data indicate that two-hit silencing of LTF through genetic and epigenetic changes may be a common and important event in the carcinogenesis of NPC.

摘要

为了研究位于常见最小缺失区域3p21.3的乳铁传递蛋白基因(LTF,也称为乳铁蛋白基因,LF)在鼻咽癌(NPC)发病机制中的作用,我们首先检测了33例原发性NPC组织和15例慢性鼻咽炎组织中该基因的表达水平。在76%(33例中的25例)的原发性NPC组织中观察到LTF表达缺失或下调。我们进一步发现,25%(20例中的5例)的NPC标本在LTF基因座处存在杂合性缺失(LOH)。通过聚合酶链反应单链构象多态性(PCR-SSCP)和DNA测序评估,在30%(20例中的6例)的原发性NPC组织中发现了LTF突变。此外,在63.6%(33例中的21例)的原发性NPC样本中发现了LTF启动子区域的高甲基化,而在慢性鼻咽炎组织中未发现。用去甲基化化合物5-氮杂-2'-脱氧胞苷处理后,NPC细胞系中的LTF转录本增加。总之,我们的数据表明,通过基因和表观遗传变化对LTF进行双打击沉默可能是NPC致癌过程中常见且重要的事件。

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