TGFBI promoter methylation is associated with poor prognosis in lung adenocarcinoma patients

Yangki Seok, Won Kee Lee, Jae Yong Park, Dong Sun Kim

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related deaths worldwide and has high rates of metastasis. Transforming growth factor beta-inducible protein (TGFBI) is an extracellular matrix component involved in tumour growth and metastasis. However, the exact role of TGFBI in NSCLC remains controversial. Gene silencing via DNA methylation of the promoter region is common in lung tumorigenesis and could thus be used for the development of molecular biomarkers. We analysed the methylation status of the TGFBI promoter in 138 NSCLC specimens via methylation-specific PCR and evaluated the correlation between TGFBI methylation and patient survival. TGFBI promoter methylation was detected in 25 (18.1%) of the tumours and was demonstrated to be associated with gene silencing. We observed no statistical correlation between TGFBI methylation and clinicopathological characteristics. Univariate and multivariate analyses showed that TGFBI methylation is significantly associated with poor survival outcomes in adenocarcinoma cases (ad-justed hazard ratio = 2.88, 95% confidence interval = 1.19-6.99, P = 0.019), but not in squamous cell cases. Our findings suggest that methylation in the TGFBI promoter may be associated with pathogenesis of NSCLC and can be used as a predictive marker for lung adenocarcinoma prognosis. Further large-scale studies are needed to confirm these findings.

Original languageEnglish
Pages (from-to)161-165
Number of pages5
JournalMolecules and Cells
Volume42
Issue number2
DOIs
StatePublished - 2019

Keywords

  • Hypermethylation
  • MSP
  • NSCLC
  • Prognosis
  • TGFBI

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