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本文引用的文献

1
Similar DNA methylation pattern in lung tumours from smokers and never-smokers with second-hand tobacco smoke exposure.二手烟暴露的吸烟者和不吸烟者的肺部肿瘤中存在相似的 DNA 甲基化模式。
Mutagenesis. 2012 Jul;27(4):423-9. doi: 10.1093/mutage/ger092. Epub 2012 Jan 4.
2
Molecular characterization of the tumor-suppressive function of nischarin in breast cancer.尼沙林在乳腺癌中抑制肿瘤功能的分子特征。
J Natl Cancer Inst. 2011 Oct 19;103(20):1513-28. doi: 10.1093/jnci/djr350. Epub 2011 Sep 14.
3
Early detection of lung cancers - Comparison of computed tomography, cytology and fuzzy-based tumor markers panels.肺癌的早期检测——计算机断层扫描、细胞学和基于模糊的肿瘤标志物联合检测的比较。
Cancer Biomark. 2010;6(3-4):149-62. doi: 10.3233/CBM-2009-0126.
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Cancer statistics, 2010.癌症统计数据,2010 年。
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7.
5
Molecular analysis of plasma DNA for the early detection of lung cancer by quantitative methylation-specific PCR.采用定量甲基化特异性 PCR 技术通过检测血浆 DNA 进行肺癌的早期诊断的分子分析。
Clin Cancer Res. 2010 Jul 1;16(13):3463-72. doi: 10.1158/1078-0432.CCR-09-3304. Epub 2010 Jun 30.
6
Childhood exposure to secondhand smoke and functional mannose binding lectin polymorphisms are associated with increased lung cancer risk.儿童时期接触二手烟和功能性甘露糖结合凝集素多态性与肺癌风险增加有关。
Cancer Epidemiol Biomarkers Prev. 2009 Dec;18(12):3375-83. doi: 10.1158/1055-9965.EPI-09-0986.
7
Cellular transformation by cigarette smoke extract involves alteration of glycolysis and mitochondrial function in esophageal epithelial cells.香烟提取物引起的细胞转化涉及食管上皮细胞糖酵解和线粒体功能的改变。
Int J Cancer. 2010 Jul 15;127(2):269-81. doi: 10.1002/ijc.25057.
8
Association between lifestyle factors and CpG island methylation in a cancer-free population.生活方式因素与癌症人群中 CpG 岛甲基化的关系。
Cancer Epidemiol Biomarkers Prev. 2009 Nov;18(11):2984-91. doi: 10.1158/1055-9965.EPI-08-1245. Epub 2009 Oct 27.
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StatBite: reported secondhand smoke exposure in the home among Americans.统计数据摘要:美国人在家中接触二手烟的情况报告。
J Natl Cancer Inst. 2008 Sep 17;100(18):1278. doi: 10.1093/jnci/djn328. Epub 2008 Sep 9.
10
Genome-wide promoter analysis uncovers portions of the cancer methylome.全基因组启动子分析揭示了癌症甲基化组的部分情况。
Cancer Res. 2008 Apr 15;68(8):2661-70. doi: 10.1158/0008-5472.CAN-07-5913.

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.

DOI:10.4161/epi.24195
PMID:23503203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3674047/
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。