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SIPA1L3 methylation modifies the benefit of smoking cessation on lung adenocarcinoma survival : an epigenomic–smoking interaction analysis

Zhang, Ruyang (author)
Harvard University,Nanjing Medical University
Lai, Linjing (author)
Nanjing Medical University
Dong, Xuesi (author)
Nanjing Medical University,Southeast University
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He, Jieyu (author)
Nanjing Medical University
You, Dongfang (author)
Nanjing Medical University
Chen, Chao (author)
Nanjing Medical University
Lin, Lijuan (author)
Nanjing Medical University
Zhu, Ying (author)
Nanjing Medical University
Huang, Hui (author)
Nanjing Medical University
Shen, Sipeng (author)
Nanjing Medical University,Harvard University
Wei, Liangmin (author)
Nanjing Medical University
Chen, Xin (author)
Nanjing Medical University
Guo, Yichen (author)
Harvard University
Liu, Liya (author)
Ningbo University
Su, Li (author)
Nanjing Medical University,Harvard University
Shafer, Andrea (author)
Massachusetts General Hospital,Harvard University
Moran, Sebastian (author)
University of Barcelona
Fleischer, Thomas (author)
Oslo university hospital
Bjaanæs, Maria Moksnes (author)
Oslo university hospital
Karlsson, Anna (author)
Lund University,Lunds universitet,Create Health,Annan verksamhet, LTH,Lunds Tekniska Högskola,Forskningsgrupp Lungcancer,Forskargrupper vid Lunds universitet,Other operations, LTH,Faculty of Engineering, LTH,Research Group Lung Cancer,Lund University Research Groups
Planck, Maria (author)
Lund University,Lunds universitet,Create Health,Annan verksamhet, LTH,Lunds Tekniska Högskola,Forskningsgrupp Lungcancer,Forskargrupper vid Lunds universitet,Other operations, LTH,Faculty of Engineering, LTH,Research Group Lung Cancer,Lund University Research Groups
Staaf, Johan (author)
Lund University,Lunds universitet,Create Health,Annan verksamhet, LTH,Lunds Tekniska Högskola,Forskningsgrupp Lungcancer,Forskargrupper vid Lunds universitet,Other operations, LTH,Faculty of Engineering, LTH,Research Group Lung Cancer,Lund University Research Groups
Helland, Åslaug (author)
Oslo university hospital,University of Oslo
Esteller, Manel (author)
University of Barcelona
Wei, Yongyue (author)
Nanjing Medical University,Harvard University
Chen, Feng (author)
Nanjing Medical University
Christiani, David C. (author)
Massachusetts General Hospital,Nanjing Medical University,Harvard University
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 (creator_code:org_t)
2019-04-17
2019
English 14 s.
In: Molecular Oncology. - : Wiley. - 1574-7891 .- 1878-0261. ; 13:5, s. 1235-1248
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Smoking cessation prolongs survival and decreases mortality of patients with non-small-cell lung cancer (NSCLC). In addition, epigenetic alterations of some genes are associated with survival. However, potential interactions between smoking cessation and epigenetics have not been assessed. Here, we conducted an epigenome-wide interaction analysis between DNA methylation and smoking cessation on NSCLC survival. We used a two-stage study design to identify DNA methylation–smoking cessation interactions that affect overall survival for early-stage NSCLC. The discovery phase contained NSCLC patients from Harvard, Spain, Norway, and Sweden. A histology-stratified Cox proportional hazards model adjusted for age, sex, clinical stage, and study center was used to test DNA methylation–smoking cessation interaction terms. Interactions with false discovery rate-q ≤ 0.05 were further confirmed in a validation phase using The Cancer Genome Atlas database. Histology-specific interactions were identified by stratification analysis in lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC) patients. We identified one CpG probe (cg02268510 SIPA 1L3 ) that significantly and exclusively modified the effect of smoking cessation on survival in LUAD patients [hazard ratio (HR) interaction = 1.12; 95% confidence interval (CI): 1.07–1.16; P = 4.30 × 10 –7 ]. Further, the effect of smoking cessation on early-stage LUAD survival varied across patients with different methylation levels of cg02268510 SIPA 1L3 . Smoking cessation only benefited LUAD patients with low methylation (HR = 0.53; 95% CI: 0.34–0.82; P = 4.61 × 10 –3 ) rather than medium or high methylation (HR = 1.21; 95% CI: 0.86–1.70; P = 0.266) of cg02268510 SIPA 1L3 . Moreover, there was an antagonistic interaction between elevated methylation of cg02268510 SIPA 1L3 and smoking cessation (HR interaction = 2.1835; 95% CI: 1.27–3.74; P = 4.46 × 10 −3 ). In summary, smoking cessation benefited survival of LUAD patients with low methylation at cg02268510 SIPA 1L3 . The results have implications for not only smoking cessation after diagnosis, but also possible methylation-specific drug targeting.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

DNA methylation
interaction analysis
molecular cancer epidemiology
non-small-cell lung cancer
overall survival
smoking cessation

Publication and Content Type

art (subject category)
ref (subject category)

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