Aurora-A overexpression as an early marker of reflux-related columnar mucosa and Barrett's oesophagus

Ann Oncol. 2007 Jun:18 Suppl 6:vi110-5. doi: 10.1093/annonc/mdm237.

Abstract

Background: The development of oesophageal adenocarcinoma is generally closely associated with the presence of a specialised intestinal-type epithelium such as that found in Barrett's oesophagus (BO). A particular histological condition is when the distal oesophagus showing cardiac and/or fundic mucosa without intestinal metaplasia cannot be defined as 'Barrett's mucosa' [condition that we call 'columnar-lined oesophagus' (CLO)] and up till now, there has been no agreement in literature about the management of this condition. Aurora-A overexpression leads to centrosome amplification, chromosomal instability and aneuploidy in mammalian cells.

Patients and methods: A prospective study was carried out on 28 consecutive patients who presented columnar mucosa above the gastro-oesophageal junction (GOJ) at endoscopy. As controls, two more biopsies were obtained, one on the normal-appearing squamous oesophagus above the GOJ, as far as possible from the columnar mucosa (controls A), and one taken 1 cm below the GOJ (controls B). The Aurora-A and p53 expression levels were analysed respectively by Quantitative Real Time PCR and immunohistochemistry.

Results: Twelve patients were affected by BO (43%) while the other 16 patients (57%) had a CLO. Nine of 28 (32%) cases were focally positive for p53 immunostaining. All the BO/CLO samples were positive for the Aurora-A transcript with regard to controls. Furthermore, 13 of 28 (46%) cases showed overexpression (above the median for the whole group).

Conclusion: Due to the low number of cases, we are not at present able to state that statistically significant quantitative differences in Aurora-A messenger RNA expression exist between CLO and BO cases with and without dysplasia and p53-positive immunostaining. Further studies on a larger number of cases with a follow-up period are necessary in order to establish the risk of progression and the correct management of these subjects.

Publication types

  • Evaluation Study

MeSH terms

  • Adenocarcinoma / enzymology
  • Adenocarcinoma / genetics
  • Adenocarcinoma / pathology
  • Adult
  • Aurora Kinases
  • Barrett Esophagus / enzymology
  • Barrett Esophagus / genetics*
  • Barrett Esophagus / pathology
  • Biomarkers / metabolism
  • Esophageal Neoplasms / enzymology
  • Esophageal Neoplasms / genetics
  • Esophageal Neoplasms / pathology
  • Female
  • Gastroesophageal Reflux / enzymology
  • Gastroesophageal Reflux / genetics*
  • Gastroesophageal Reflux / pathology
  • Humans
  • Male
  • Middle Aged
  • Mucous Membrane / enzymology
  • Mucous Membrane / pathology
  • Prospective Studies
  • Protein Serine-Threonine Kinases / biosynthesis*
  • Protein Serine-Threonine Kinases / genetics*

Substances

  • Biomarkers
  • Aurora Kinases
  • Protein Serine-Threonine Kinases