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香烟烟雾会诱导肿瘤抑制基因NISCH发生甲基化。

Cigarette smoke induces methylation of the tumor suppressor gene NISCH.

作者信息

Ostrow Kimberly Laskie, Michailidi Christina, Guerrero-Preston Rafael, Hoque Mohammad O, Greenberg Alissa, Rom William, Sidransky David

机构信息

Department of Otolaryngology; Head and Neck Cancer Research Division; Johns Hopkins School of Medicine; Baltimore, MD USA.

Department of Medicine; New York University; New York, NY USA.

出版信息

Epigenetics. 2013 Apr;8(4):383-8. doi: 10.4161/epi.24195. Epub 2013 Mar 15.

Abstract

We have previously identified a putative tumor suppressor gene, NISCH, whose promoter is methylated in lung tumor tissue as well as in plasma obtained from lung cancer patients. NISCH was observed to be more frequently methylated in smoker lung cancer patients than in non-smoker lung cancer patients. Here, we investigated the effect of tobacco smoke exposure on methylation of the NISCH gene. We tested methylation of NISCH after oral keratinocytes were exposed to mainstream and side stream cigarette smoke extract in culture. Methylation of the promoter region of the NISCH gene was also evaluated in plasma obtained from lifetime non-smokers and light smokers (<20 pack/year), with and without lung tumors, and heavy smokers (20+ pack/year) without disease. Promoter methylation of NISCH was tested by quantitative fluorogenic real-time PCR in all samples. Promoter methylation of NISCH occurred after exposure to mainstream tobacco smoke as well as to side stream tobacco smoke in normal oral keratinocyte cell lines. NISCH methylation was also detected in 68% of high-risk, heavy smokers without detectable tumors. Interestingly, in light smokers, NISCH methylation was present in 69% of patients with lung cancer and absent in those without disease. Our pilot study indicates that tobacco smoke induces methylation changes in the NISCH gene promoter before any detectable cancer. Methylation of the NISCH gene was also found in lung cancer patients' plasma samples. After confirming these findings in longitudinally collected plasma samples from high-risk populations (such as heavy smokers), examining patients for hypermethylation of the NISCH gene may aid in identifying those who should undergo additional screening for lung cancer.

摘要

我们之前鉴定出一个假定的肿瘤抑制基因NISCH,其启动子在肺肿瘤组织以及肺癌患者的血浆中发生甲基化。据观察,与非吸烟肺癌患者相比,吸烟肺癌患者中NISCH甲基化更为常见。在此,我们研究了烟草烟雾暴露对NISCH基因甲基化的影响。我们在培养中使口腔角质形成细胞暴露于主流和侧流香烟烟雾提取物后,检测了NISCH的甲基化情况。还对从未吸烟者和轻度吸烟者(<20包/年)(有或无肺肿瘤)以及无疾病的重度吸烟者(≥20包/年)的血浆中NISCH基因启动子区域的甲基化进行了评估。所有样本均通过定量荧光实时PCR检测NISCH的启动子甲基化。在正常口腔角质形成细胞系中,暴露于主流烟草烟雾以及侧流烟草烟雾后均发生了NISCH启动子甲基化。在68%无可检测肿瘤的高危重度吸烟者中也检测到了NISCH甲基化。有趣的是,在轻度吸烟者中,69%的肺癌患者存在NISCH甲基化,而无疾病者则不存在。我们的初步研究表明,在任何可检测到的癌症出现之前,烟草烟雾会诱导NISCH基因启动子的甲基化变化。在肺癌患者的血浆样本中也发现了NISCH基因的甲基化。在从高危人群(如重度吸烟者)纵向收集的血浆样本中证实这些发现后,检测患者的NISCH基因高甲基化可能有助于识别那些应接受额外肺癌筛查的人群。

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