Clinical Epigenetics (Mar 2019)

SOX2 promoter hypermethylation in non-smoking Taiwanese adults residing in air pollution areas

  • Disline Manli Tantoh,
  • Ming-Fang Wu,
  • Chien-Chang Ho,
  • Chia-Chi Lung,
  • Kuan-Jung Lee,
  • Oswald Ndi Nfor,
  • Yi-Chia Liaw,
  • Shu-Yi Hsu,
  • Pei-Hsin Chen,
  • Chin Lin,
  • Hou-Wei Chu,
  • Yi-Ching Liaw,
  • Yung-Po Liaw

DOI
https://doi.org/10.1186/s13148-019-0647-8
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 7

Abstract

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Abstract Background Both SOX2 promoter methylation and air pollution have been associated with lung cancer risk. However, little has been done to assess SOX2 promoter methylation in individuals living in air pollution areas. The aim of this study was to investigate SOX2 promoter methylation in non-smoking Taiwanese adults living in areas with different levels of air pollution especially particulate matter with diameter < 2.5 μm (PM2.5). Methods A total of 1142 individuals aged 30–70 years were recruited. Data on SOX2 methylation, residence, age, and exposure to second-hand smoke (SHS) among others were extracted from the Taiwan Biobank dataset (2008–2015). After excluding former and current smokers, alongside those with incomplete information, a total of 461 non-smokers comprising 176 men and 285 women were included in the study. Participants’ residences were grouped under northern and central/southern areas because air pollution (PM2.5) is lower in northern compared to central and southern areas. Results The methylation levels in men (0.16310 ± 0.01230) and women (0.15740 ± 0.01240) were significantly different (P < .0001). In both sexes, the SOX2 promoter region was shown to be significantly hypermethylated in central and southern areas compared with the northern areas. The regression coefficient (β) was 0.00331 (P = 0.0257) in men and 0.00514 (P < .0001) in women. Conclusion SOX2 was significantly hypermethylated in both men and women residing in central and southern areas. The consistency in the results for both sexes shows that SOX2 promoter methylation could serve as a potential biomarker for industrial air pollution exposure. Moreover, it might reflect predisposition to cancer. Hence, healthy non-smokers at precancerous stages who have not been clinically diagnosed could be identified.

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