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Oesophageal squamous cell carcinoma may develop within a background of accumulating DNA methylation in normal and dysplastic mucosa
  1. T Ishii1,
  2. J Murakami2,
  3. K Notohara3,
  4. H M Cullings4,
  5. H Sasamoto1,
  6. T Kambara1,
  7. Y Shirakawa1,
  8. Y Naomoto1,
  9. M Ouchida5,
  10. K Shimizu5,
  11. N Tanaka1,
  12. J R Jass6,
  13. N Matsubara1
  1. 1Department of Gastroenterological Surgery and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan
  2. 2Department of Oral and Maxillofacial Radiology, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan
  3. 3Department of Pathological Research, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan
  4. 4Department of Statistics, Radiation Effects Research Foundation, Hiroshima, Japan
  5. 5Department of Molecular Genetics, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan
  6. 6Department of Pathology, McGill University, Montreal, Quebec, Canada
  1. Correspondence to:
    Dr N Matsubara
    Department of Gastroenterological Surgery and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, 2-5-1, Shikata-cho, Okayama 700-8558, Japan; nagamb{at}cc.okayama-u.ac.jp

Abstract

Background: Oesophageal squamous cell carcinoma (OSCC) often arises from preceding dysplastic lesions in the oesophageal epithelium. However, the molecular changes occurring in premalignant lesions are not well understood. An epigenetic change is an example of OSCC that may occur within the epithelium.

Aim: To investigate the methylation status of multiple promoters in cancer-derived DNA, as well as in the background epithelium of OSCC, including dysplastic lesions and non-neoplastic mucosa. The normal epithelium from patients without cancer was also examined. The findings were correlated with the mutational status of p53.

Patients and methods: 56 patients with advanced OSCC, 21 patients with intraepithelial neoplasia (IEN), 56 patients with a background of non-neoplastic epithelium, adjacent to the OSCC, and 42 normal control epithelia from healthy volunteers were studied. The promoter methylation status of SFRP1, SFRP2, DCC, APC, p16INK4a, p14ARF, MINT1, MINT2, MINT31, CACNA1G, COX2, DAPK, hMLH1 and MGMT was examined by methylation-specific single polymerase chain reaction or combined bisulphite restriction analysis. The mutation of p53 by direct sequencing was assessed.

Results: DNA methylation was observed in OSCC and in its background epithelium. The frequency of CpG island methylation increased from a baseline level in the background non-neoplastic epithelium, through IEN, to advanced OSCC. However, mutations in p53 were almost exclusively observed in IEN and OSCC. More extensive DNA methylation was seen in the neoplastic lesions (OSCC or IEN) having a p53 mutation than in those with wild-type p53.

Conclusion: DNA methylation is present at low levels in the non-neoplastic oesophageal epithelium and appears to contribute to the progression of the dysplasia–carcinoma sequence in OSCC carcinogenesis.

  • COBRA, combined bisulphite restriction analysis
  • OSCC, oesophageal squamous cell carcinoma
  • H&E, haematoxylin and eosin
  • IEN, intraepithelial neoplasia
  • PAS, periodic acid schiff
  • PCR, polymerase chain reaction
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Footnotes

  • Published Online First 9 June 2006

  • OSCC, oesophageal squamous cell carcinoma.

  • Competing interests: None declared.

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