期刊论文详细信息
Tobacco Induced Diseases
Effect of cigarette smoke condensate on gene promoter methylation in human lung cells
George Hammons1  Beverly Lyn-Cook1  Nysia George1  Beverly Word1  Lascelles Lyn-Cook1 
[1] HFT-100, Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA
关键词: Lung cancer cells;    Cigarette smoke condensate;    DNA methylation;   
Others  :  1135287
DOI  :  10.1186/1617-9625-12-15
 received in 2014-03-14, accepted in 2014-08-28,  发布年份 2014
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【 摘 要 】

Background

In lung cancer, an association between tobacco smoking and promoter DNA hypermethylation has been demonstrated for several genes. However, underlying mechanisms for promoter hypermethylation in tobacco-induced cancer are yet to be fully established.

Methods

Promoter methylation was evaluated in control and cigarette smoke condensate (CSC) exposed human lung cells using the Methyl-Profiler DNA Methylation PCR System. PSAE cells were exposed to 0.3 or 1.0 μg/ml CSC for 72 hours and longer term for 14 and 30 days. NL-20 cells were exposed for 30 days to 10 or 100 μg/ml CSC.

Results

Promoters of several genes, including hsa-let-7a-3, CHD1, CXCL12, PAX5, RASSF2, and TCF21, were highly methylated (>90%); hsa-let-7a-3 was affected in both cell lines and under all exposure conditions. Level of methylation tended to increase with CSC concentration and exposure duration (statistical differences were not determined). Percentage methylation of TCF21, which was >98% at exposures of 10 or 100 μg/ml CSC, was found to be reduced to 28% and 42%, respectively, in the presence of the dietary agent genistein.

Conclusions

Using array techniques, several tumor suppressor genes in human lung cells were identified that undergo promoter hypermethylation, providing further evidence of their potential involvement in tobacco smoke-induced lung carcinogenesis and their use as potential biomarkers of harm in tobacco smoke exposure. Results from the study also demonstrated the potential of a dietary agent to exert chemopreventive activity in human tissue against tobacco smoke related diseases through modulation of DNA methylation. Additional studies are needed to confirm these findings.

【 授权许可】

   
2014 Lyn-Cook et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Molina JR, Yang P, Cassivi SD, Schild SE, Adjei AA: Non-small-cell lung cancer: epidemiology, risk factors, treatment, and survivorship. Mayo Clin Proc 2008, 83:584-594.
  • [2]Alberg AJ, Ford JG, Samet JM: Epidemiology of lung cancer ACCP evidence-based clinical practice guidelines (2nd Edition). Chest 2007, 132(Suppl. 3):29S-55S.
  • [3]Khuder SS: Effect of cigarette smoking on major histological types of lung cancer: a meta-analysis. Lung Cancer 2001, 31:139-148.
  • [4]Besaratinia A, Pfeifer GP: Second-hand smoke and human lung cancer. Lancet Oncol 2008, 9:657-666.
  • [5]Esteller M: Epigenetics in cancer. N Engl J Med 2008, 358:1148-1159.
  • [6]Zochbauer-Muller S, Minna JD, Gazdar AF: Aberrant DNA methylation in lung cancer: biological and clinical implications. Oncologist 2002, 7:451-457.
  • [7]Belinsky SA, Nikuja KJ, Palmisano WA, Michels R, Saccomanno G, Gabrielson E, Baylin SB, Herman JG: Aberrant methylation of p16(INK4a) is an early event in lung cancer and a potential biomarker for early diagnosis. Proc Natl Acad Sci U S A 1998, 95:11891-11896.
  • [8]Rauch T, Wang Z, Zhang X, Zhong X, Wu X, Lau SK, Kernstine KH, Riggs AD, Pfeifer GP: Homebox gene methylation in lung cancer studied by genome-wide analysis with a microarray-based methylated CpG island recovery assay. Proc Natl Acad Sci U S A 2007, 104:5527-5532.
  • [9]Rauch TA, Zhong X, Wu X, Wang M, Kernstine KH, Wang Z, Riggs AD, Pfeifer GP: High-resolution mapping of DNA hypermethylation and hypomethylation in lung cancer. Proc Natl Acad Sci U S A 2008, 105:252-257.
  • [10]Kim DH, Nelson HH, Wiencke JK, Christiani DC, Wain JC, Mark EJ, Kelsey KT: Promoter methylation of DAP-kinase: association with advanced stage in non-small cell lung cancer. Oncogene 2001, 20:1765-1770.
  • [11]Hammons G, Lyn-Cook B: Epigenetics in tobacco smoke toxicology. Curr Top Toxicol 2011, 7:63-77.
  • [12]Osada H, Takahashi T: let-7 and miR-17-92: Small-sized major players in lung cancer development. Cancer Sci 2011, 102:9-17.
  • [13]Wang X, Cao L, Wang Y, Wang X, Liu N, Yoou Y: Regulation of let-7 and its target oncogenes (Review). Oncol Lett 2012, 3:955-960.
  • [14]Vrba L, Munoz-Rodriquez JL, Stampfer MR, Futscher BW: miRNA gene promoters are frequent targets of aberrant methylation in human breast cancer. PLoS One 2013, 8:e54398.
  • [15]Brueckner B, Stresemann C, Kuner R, Mund C, Musch T, Meister M, Sultmann H, Lyklo F: The human let7a-3 locus contains an epigenetically regulated microRNA gene with oncogenic function. Cancer Res 2007, 67:1419-1423.
  • [16]Lu L, Katsaros D, de la Longrais IA R, Sochirca O, Yu H: Hypermethylation of let-7a-3 in epithelial ovarian cancer is associated with low insulin-like growth factor-II expression and favorable prognosis. Cancer Res 2007, 67:10117-10122.
  • [17]Izzotti A, Calin GA, Arrigo P, Steele VE, Croce CM, De Flora S: Down regulation of microRNA expression in the lungs of rats exposed to cigarette smoke. FASEB J 2009, 23:806-812.
  • [18]Izzotti A, Larghero P, Longobardi M, Cartiglia C, Camoirona A, Steele VE, De Flora S: Dose-responsiveness and persistence of microRNA expression alterations induced by cigarette smoke in mouse lung. Mutat Res 2011, 717:9-16.
  • [19]Zhang Y, Chen H: Genistein, an epigenome modifier during cancer prevention. Epigenetics 2011, 6:888-891.
  • [20]Adjakly M, Bosviel R, Rabiau N, Boiteux J-P, Bignon Y-J, Guy L, Bernard-Gallon D: DNA methylation and soy phyotestrogens: quantitative study in DU-145 and PC-3 human prostate cancer cell lines. Epigenomics 2011, 3:795-803.
  • [21]Quaggin SE, Schwartz L, Cui S: The basic-helix-loop-helix protein pod1 is critically important for kidney and lung organogenesis. Development 1999, 126:5771-5783.
  • [22]Smith LT, Lin M, Brena RM, Lang JC, Schuller DE, Otterson GA, Morrison CD, Smiraglia DJ, Plass C: Epigenetic regulation of the tumor suppressor gene TCF21 on 6q23-q24 in lung and head and neck cancer. Proc Natl Acad Sci U S A 2006, 103:982-987.
  • [23]Hellermann GR, Nagy SB, Kong X, Lockey RF, Mohapatra SS: Mechanism of cigarette smoke condensate-induced acute inflammatory response in human bronchial epithelial cells. Respir Res 2002, 3:22. BioMed Central Full Text
  • [24]Nagathihalli NS, Massion PP, Gonzalez AL, Lu P, Datta PK: Smoking induces epithelial-to-mesenchymal transition to non-small cell lung cancer through HDAC-mediated downregulation of E-cadherin. Mol Cancer Ther 2012, 11:2362-2372.
  • [25]Nagaraj NS, Beckers S, Mensah JK, Waigel S, Vigneswaran N, Zacharias W: Cigarette smoke condensate induces cytochromes P450 and aldo-keto reductases in oral cancer cells. Toxicol Lett 2006, 165:182-194.
  • [26]Xu H, Ferro TJ, Chu S: Cigarette smoke condensate inhibits ENaC α-subunit expression in lung epithelial cells. Eur Respir J 2007, 30:633-642.
  • [27]Shizu M, Itoh Y, Sunahara R, Chujo S, Hayashi H, Ide Y, Takii T, Koshiko M, Chung SW, Hayakawa K, Miyazawa K, Hirose K, Onozaki K: Cigarette smoke condensate upregulates the gene and protein expression of proinflammatory cytokines in human fibroblast-like synoviocyte line. J Interferon Cytokine Res 2008, 28:509-522.
  • [28]Calafat AM, Polzin GM, Saylor J, Richter P, Ashley DL, Watson CH: Determination of tar, nicotine, and carbon monoxide yields in the mainstream smoke of selected international cigarettes. Tob Control 2004, 13:45-51.
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