Alteration of DNA methyltransferases contributes to 5′CpG methylation and poor prognosis in lung cancer

Ruo Kai Lin, Han Shui Hsu, Jer Wei Chang, Chih Yi Chen, Jung Ta Chen, Yi Ching Wang

Research output: Contribution to journalArticlepeer-review

205 Citations (Scopus)


Overexpression of DNA methyltransferases DNMT1, DNMT3a and DNMT3b has been reported in various cancers. However, physical binding of DNA methyltransferase (DNMT) to the hypermethylated promoter of tumor suppressor genes (TSGs) has never been demonstrated in tumor tissues. In addition, alteration of DNMT at the protein level has never been reported in the same series of cancer patients. By immunohistochemical analysis, we demonstrated that DNMT1, DNMT3a and DNMT3b proteins were highly expressed in a coordinate manner in lung tumors, particularly in smokers (P = 0.037, by the Fisher exact test). Patients with DNMT1 overexpression had a trend of poorer prognosis than those without such overexpression, and this prognostic significance was apparent in squamous carcinoma (SQ) patients (P = 0.041, by the log-rank test). Both DNMT1 and DNMT3b overexpressions correlated with hypermethylation in the TSG promoters, especially among smoking SQ patients (P = 0.012). To further explore the molecular mechanisms between altered TSGs promoter methylation and overexpression of DNMTs protein, we performed a tissue chromatin-immunoprecipitation polymerase chain reaction assay for lung tumors and showed that the methylated FHIT, p16INK4a and RARβ promoters were bound by both DNMT protein and methyl-CpG-binding protein 2. These data suggest that overexpression and strong binding of various DNMTs may result in promoter hypermethylation of multiple TSGs and ultimately lead to lung tumorigenesis and poor prognosis.

Original languageEnglish
Pages (from-to)205-213
Number of pages9
JournalLung Cancer
Issue number2
Publication statusPublished - Feb 2007
Externally publishedYes


  • 5′CpG hypermethylation
  • DNMT
  • Immunohistochemistry
  • MeCP2
  • Tissue chromatin immunoprecipitation

ASJC Scopus subject areas

  • Oncology
  • Pulmonary and Respiratory Medicine
  • Cancer Research


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