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A comparison of primary oesophageal squamous epithelial cells with HET-1A in organotypic culture

A comparison of primary oesophageal squamous epithelial cells with HET-1A in organotypic culture
A comparison of primary oesophageal squamous epithelial cells with HET-1A in organotypic culture
Background Information: Carcinoma of the oesophagus is the 6th leading cause of cancer death in the western world and is associated with a 5-year survival of less than 15%. Recent evidence suggests that stromal-epithelial interactions are fundamental in carcinogenesis. The advent of co-culture techniques permits the investigation of cross-talk between the stroma and epithelium in a physiological setting. We have characterised a histologically representative oesophageal organotypic model, and used it to compare the most commonly used squamous oesophageal cell line, HET-1A, with primary oesophageal squamous cells for use in studies of the oesophageal epithelium in vitro.

Results: When grown in an organotypic culture with normal fibroblasts the oesophageal carcinoma cell lines OE21 (squamous) and OE19 (adenocarcinoma) morphologically resembled the tumour of origin with evidence of stromal invasion and mucus production respectively. However, HET-1A cells, which were derived from normal squamous oesophageal cells, appeared dysplastic and failed to display evidence of squamous differentiation. By comparison with primary oesophageal epithelial cells the HET-1A cells were highly proliferative and did not express the epithelial markers E-cadherin or CK5/6, or the stratified epithelial marker ?Np63, but did express the mesenchymal markers vimentin and N-cadherin.

Conclusion: Studies of epithelial carcinogenesis will benefit from culture systems which allow the manipulation of the stromal and epithelial layers independently. We have developed an organotypic culture using primary oesophageal squamous cells and fibroblasts in which a stratified epithelium with a proliferative basal layer that stains strongly for ?Np63 develops. This model will be suitable for the study of the molecular events in the development of Barrett's oesophagus. The most commonly used normal oesophageal squamous cell line, HET-1A, does not have the characteristics of normal oesophageal squamous cells, and should not be used in models of the normal oesophageal epithelium. Until more representative cell lines are available, future studies in oesophageal cancer will be reliant on the availability and manipulation of primary tissue.
het-1A, oesophageal carcinoma, organotypic model, p63
0248-4900
635-644
Underwood, Timothy J.
8e81bf60-edd2-4b0e-8324-3068c95ea1c6
Derouet, Mathieu F.
42a705c7-4556-441a-996d-6d0845146f41
White, Michael J.
fcbaf8a0-d2ec-4dd2-9aa5-4a252ab95d58
Noble, Fergus
4f14574c-28f2-4e04-bd95-f53c7649e1fa
Moutasim, Karwan A.
af7dd711-f6df-44f7-8c57-052bf15303af
Smith, Eric
d2445970-3034-4a7f-9465-87f79f636ea6
Drew, Paul A.
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Thomas, Gareth J.
2ff54aa9-a766-416b-91ee-cf1c5be74106
Primrose, John N.
d85f3b28-24c6-475f-955b-ec457a3f9185
Blaydes, Jeremy P.
e957f999-fd91-4f77-ad62-5b4ef069b15b
Underwood, Timothy J.
8e81bf60-edd2-4b0e-8324-3068c95ea1c6
Derouet, Mathieu F.
42a705c7-4556-441a-996d-6d0845146f41
White, Michael J.
fcbaf8a0-d2ec-4dd2-9aa5-4a252ab95d58
Noble, Fergus
4f14574c-28f2-4e04-bd95-f53c7649e1fa
Moutasim, Karwan A.
af7dd711-f6df-44f7-8c57-052bf15303af
Smith, Eric
d2445970-3034-4a7f-9465-87f79f636ea6
Drew, Paul A.
3312262e-cf84-45d3-a555-f80f315bd361
Thomas, Gareth J.
2ff54aa9-a766-416b-91ee-cf1c5be74106
Primrose, John N.
d85f3b28-24c6-475f-955b-ec457a3f9185
Blaydes, Jeremy P.
e957f999-fd91-4f77-ad62-5b4ef069b15b

Underwood, Timothy J., Derouet, Mathieu F., White, Michael J., Noble, Fergus, Moutasim, Karwan A., Smith, Eric, Drew, Paul A., Thomas, Gareth J., Primrose, John N. and Blaydes, Jeremy P. (2010) A comparison of primary oesophageal squamous epithelial cells with HET-1A in organotypic culture. Biology of the Cell, 102, 635-644. (doi:10.1042/BC20100071). (PMID:20843300)

Record type: Article

Abstract

Background Information: Carcinoma of the oesophagus is the 6th leading cause of cancer death in the western world and is associated with a 5-year survival of less than 15%. Recent evidence suggests that stromal-epithelial interactions are fundamental in carcinogenesis. The advent of co-culture techniques permits the investigation of cross-talk between the stroma and epithelium in a physiological setting. We have characterised a histologically representative oesophageal organotypic model, and used it to compare the most commonly used squamous oesophageal cell line, HET-1A, with primary oesophageal squamous cells for use in studies of the oesophageal epithelium in vitro.

Results: When grown in an organotypic culture with normal fibroblasts the oesophageal carcinoma cell lines OE21 (squamous) and OE19 (adenocarcinoma) morphologically resembled the tumour of origin with evidence of stromal invasion and mucus production respectively. However, HET-1A cells, which were derived from normal squamous oesophageal cells, appeared dysplastic and failed to display evidence of squamous differentiation. By comparison with primary oesophageal epithelial cells the HET-1A cells were highly proliferative and did not express the epithelial markers E-cadherin or CK5/6, or the stratified epithelial marker ?Np63, but did express the mesenchymal markers vimentin and N-cadherin.

Conclusion: Studies of epithelial carcinogenesis will benefit from culture systems which allow the manipulation of the stromal and epithelial layers independently. We have developed an organotypic culture using primary oesophageal squamous cells and fibroblasts in which a stratified epithelium with a proliferative basal layer that stains strongly for ?Np63 develops. This model will be suitable for the study of the molecular events in the development of Barrett's oesophagus. The most commonly used normal oesophageal squamous cell line, HET-1A, does not have the characteristics of normal oesophageal squamous cells, and should not be used in models of the normal oesophageal epithelium. Until more representative cell lines are available, future studies in oesophageal cancer will be reliant on the availability and manipulation of primary tissue.

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More information

Published date: 15 September 2010
Keywords: het-1A, oesophageal carcinoma, organotypic model, p63

Identifiers

Local EPrints ID: 164155
URI: http://eprints.soton.ac.uk/id/eprint/164155
ISSN: 0248-4900
PURE UUID: 04d5d130-1429-4e39-b430-b7b88bd9b441
ORCID for Timothy J. Underwood: ORCID iD orcid.org/0000-0001-9455-2188
ORCID for John N. Primrose: ORCID iD orcid.org/0000-0002-2069-7605
ORCID for Jeremy P. Blaydes: ORCID iD orcid.org/0000-0001-8525-0209

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Date deposited: 23 Dec 2010 11:41
Last modified: 14 Mar 2024 02:48

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Contributors

Author: Mathieu F. Derouet
Author: Michael J. White
Author: Fergus Noble
Author: Eric Smith
Author: Paul A. Drew

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