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Journal of Clinical Pathology 2004;57:1063-1068; doi:10.1136/jcp.2003.015727
Copyright © 2004 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.
Journal of Clinical Pathology 2004;57:1063-1068
© 2004 BMJ Publishing Group Ltd & Association of Clinical Pathologists

ORIGINAL ARTICLE

The homeodomain protein CDX2 is an early marker of Barrett’s oesophagus

L M G Moons1, D A Bax1, E J Kuipers1, H van Dekken2, J Haringsma1, A H M van Vliet1, P D Siersema1 and J G Kusters1

1 Department of Gastroenterology and Hepatology, Erasmus MC–University Medical Centre Rotterdam, 3015 GD Rotterdam, The Netherlands
2 Department of Pathology, Erasmus MC–University Medical Centre Rotterdam

Correspondence to:
Correspondence to:
Dr J G Kusters
Department of Gastroenterology and Hepatology, Erasmus MC–University Medical Centre Rotterdam, L-459, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands; j.g.kusters{at}erasmusmc.nl

Background: In Barrett’s oesophagus (BO), squamous epithelium is replaced by specialised intestinal epithelium (SIE). Transcription factors associated with intestinal differentiation, such as CDX2, may be involved in BO development.

Aim: To investigate CDX2 expression in BO, squamous epithelium, and oesophageal adenocarcinoma (ADC).

Methods: CDX2 expression was assessed in 245 samples—167 biopsies of the columnar lined segment and 38 squamous epithelial biopsies of 39 patients with histologically confirmed BO (10 with ADC). Forty biopsies from 20 patients with reflux oesophagitis (RO) without BO were also evaluated. CDX2 protein was investigated immunohistochemically in 138 biopsies from 16 patients with BO, four with ADC, and 20 with RO. Cdx2 and Muc2 mRNA were detected semiquantitatively using 88 BO biopsies and squamous epithelium from 19 BO patients, and when present from ADC.

Results: SIE was present in 53/79 biopsies from the columnar lined segment; CDX2 protein was seen in all epithelial cells, but not in biopsies containing only gastric metaplastic epithelium (26/79), or in squamous epithelium (0/40) of patients with RO. Cdx2 mRNA was detected in all biopsies with goblet cell specific Muc2 transcription—indicative of SIE. Low Cdx2 mRNA expression was seen in 6/19 squamous epithelium samples taken 5 cm above the squamocolumnar junction of BO patients.

Conclusion: CDX2 protein/mRNA is strongly associated with oesophageal SIE. Cdx2 mRNA was present in the normal appearing squamous epithelium of one third of BO patients, and may precede morphological changes seen in BO. Therefore, pathways that induce Cdx2 transcription in squamous epithelial cells may be important in BO development.

Abbreviations: BO, Barrett’s oesophagus; GORD, gastro-oesophageal reflux disease; PCR, polymerase chain reaction; RT, reverse transcription; SIE, specialised intestinal epithelium

Keywords: Barrett’s oesophagus; gastro-oesophageal reflux disease; CDX2; reflux oesophagagitis


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