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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Cigarette smoke induces promoter methylation of single-stranded DNA-binding protein 2 in human esophageal squamous cell carcinoma.
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Cigarette smoke induces promoter methylation of single-stranded DNA-binding protein 2 in human esophageal squamous cell carcinoma.

机译:香烟烟雾诱导人食管鳞状细胞癌中单链DNA结合蛋白2的启动子甲基化。

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摘要

Esophageal squamous cell carcinoma (ESCC) is the sixth most frequent cause of cancer death in the world, and cigarette smoke is a key factor in esophageal carcinogenesis. To identify molecular changes during cigarette smoke-induced ESCC, we examined the methylation status of 13 gene promoters in the human immortalized, nontumorigenic esophageal epithelial cell line (Het-1A) that were exposed to mainstream (MSE) or sidestream cigarette smoke extract (SSE) for 6 months in culture. The promoter of sequence-specific single-stranded DNA-binding protein 2 (SSBP2) was methylated in the Het-1A cells exposed to MSE (MSE-Het-1A). Promoter methylation (86%, 56/70) and downregulation of SSBP2 expression were frequently detected in tumor tissues from ESCC patients. In addition, reintroduction of SSBP2 in an ESCC cell line (TE1) that does not express SSBP2 and in the MSE-Het-1A cells inhibited expression of LRP6 and Dvl3, which are mediators of the Wnt signaling pathway. SSBP2 expression markedly decreased the colony-forming ability of ESCC cell lines and significantly inhibited cell growth of the MSE-Het-1A cells. Our results indicate that cigarette smoking is a cause of SSBP2 promoter methylation and that SSBP2 harbors a tumor suppressive role in ESCC through inhibition of the Wnt signaling pathway.
机译:食道鳞状细胞癌(ESCC)是世界上第六大最常见的癌症死亡原因,而香烟烟雾是食道癌变的关键因素。为了确定香烟烟雾诱导的ESCC过程中的分子变化,我们检查了人类永生化,非致瘤性食管上皮细胞系(Het-1A)中暴露于主流(MSE)或侧流香烟烟雾提取物(SSE)中13个基因启动子的甲基化状态)培养6个月。序列特异性单链DNA结合蛋白2(SSBP2)的启动子在暴露于MSE(MSE-Het-1A)的Het-1A细胞中被甲基化。在ESCC患者的肿瘤组织中经常检测到启动子甲基化(86%,56/70)和SSBP2表达下调。此外,在不表达SSBP2的ESCC细胞系(TE1)和MSE-Het-1A细胞中重新引入SSBP2抑制了LRP6和Dvl3的表达,它们是Wnt信号通路的介体。 SSBP2表达显着降低了ESCC细胞系的集落形成能力,并显着抑制了MSE-Het-1A细胞的细胞生长。我们的结果表明,吸烟是SSBP2启动子甲基化的原因,并且SSBP2通过抑制Wnt信号通路在ESCC中具有肿瘤抑制作用。

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