Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines

In view of the potential uses of cell surface tumour associated antigens in novel anticancer treatment. a study was designed to investigate whether the biological response modifiers interferon-gamma (IFN-γ) and tumour necrosis factor-alpha (TNF-α) could effect the expression of an epitope on the tum...

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Main Authors: Sean Clark, Michael A. Mcguckin, Terry Hurst, Bruce G. Ward
Format: Article
Language:English
Published: Hindawi Limited 1994-01-01
Series:Disease Markers
Online Access:http://dx.doi.org/10.1155/1994/480236
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spelling doaj-28ceb9ef1fc243afaedb4966f2f2ef512020-11-24T22:31:05ZengHindawi LimitedDisease Markers0278-02401875-86301994-01-01121435010.1155/1994/480236Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell LinesSean Clark0Michael A. Mcguckin1Terry Hurst2Bruce G. Ward3Department of Obstetrics And Gynaecology, University of Queensland, Clinical Sciences Building, Royal Brisbane Hospital, Henton 4029, AustraliaDepartment of Obstetrics And Gynaecology, University of Queensland, Clinical Sciences Building, Royal Brisbane Hospital, Henton 4029, AustraliaDepartment of Obstetrics And Gynaecology, University of Queensland, Clinical Sciences Building, Royal Brisbane Hospital, Henton 4029, AustraliaDepartment of Obstetrics And Gynaecology, University of Queensland, Clinical Sciences Building, Royal Brisbane Hospital, Henton 4029, AustraliaIn view of the potential uses of cell surface tumour associated antigens in novel anticancer treatment. a study was designed to investigate whether the biological response modifiers interferon-gamma (IFN-γ) and tumour necrosis factor-alpha (TNF-α) could effect the expression of an epitope on the tumour associated MUC I epithelial mucin. Four ovarian carcinoma cell lines showing high (OAW42 and GG) and low (JAM and PEO1) basal expression of MUC1 were treated with 10-1000 U/mL of IFN-γor TNF-α for one or five days. Changes in MUC1 expression in cells exposed to IFN-γ or TNF-α were monitored using an ELISA technique with the monoclonal antibody BC2 which reacts with a core protein epitope on the MUC1 mucin, and then corrected for the number of viable cells present. TNF-α had little effect on MUC1 expression, but one or five days exposure to IFN-γ significantly increased MUC1 expression (p < 0.01) in all cell lines including the two cell lines that initially showed little or no expression.http://dx.doi.org/10.1155/1994/480236
collection DOAJ
language English
format Article
sources DOAJ
author Sean Clark
Michael A. Mcguckin
Terry Hurst
Bruce G. Ward
spellingShingle Sean Clark
Michael A. Mcguckin
Terry Hurst
Bruce G. Ward
Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines
Disease Markers
author_facet Sean Clark
Michael A. Mcguckin
Terry Hurst
Bruce G. Ward
author_sort Sean Clark
title Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines
title_short Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines
title_full Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines
title_fullStr Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines
title_full_unstemmed Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines
title_sort effect of interferon-γ and tnf-α on mucl mucin expression in ovarian carcinoma cell lines
publisher Hindawi Limited
series Disease Markers
issn 0278-0240
1875-8630
publishDate 1994-01-01
description In view of the potential uses of cell surface tumour associated antigens in novel anticancer treatment. a study was designed to investigate whether the biological response modifiers interferon-gamma (IFN-γ) and tumour necrosis factor-alpha (TNF-α) could effect the expression of an epitope on the tumour associated MUC I epithelial mucin. Four ovarian carcinoma cell lines showing high (OAW42 and GG) and low (JAM and PEO1) basal expression of MUC1 were treated with 10-1000 U/mL of IFN-γor TNF-α for one or five days. Changes in MUC1 expression in cells exposed to IFN-γ or TNF-α were monitored using an ELISA technique with the monoclonal antibody BC2 which reacts with a core protein epitope on the MUC1 mucin, and then corrected for the number of viable cells present. TNF-α had little effect on MUC1 expression, but one or five days exposure to IFN-γ significantly increased MUC1 expression (p < 0.01) in all cell lines including the two cell lines that initially showed little or no expression.
url http://dx.doi.org/10.1155/1994/480236
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