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MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells

The mucin MUC4 is a high molecular weight transmembrane glycoprotein. It consists of a mucin-type subunit (MUC4α) and a transmembrane growth factor-like subunit (MUC4β). The mucin MUC4 is overexpressed in many epithelial malignancies including ovarian cancer, suggesting a possible role in the pathog...

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Autores principales: Ponnusamy, M P, Singh, A P, Jain, M, Chakraborty, S, Moniaux, N, Batra, S K
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527793/
https://www.ncbi.nlm.nih.gov/pubmed/18665193
http://dx.doi.org/10.1038/sj.bjc.6604517
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author Ponnusamy, M P
Singh, A P
Jain, M
Chakraborty, S
Moniaux, N
Batra, S K
author_facet Ponnusamy, M P
Singh, A P
Jain, M
Chakraborty, S
Moniaux, N
Batra, S K
author_sort Ponnusamy, M P
collection PubMed
description The mucin MUC4 is a high molecular weight transmembrane glycoprotein. It consists of a mucin-type subunit (MUC4α) and a transmembrane growth factor-like subunit (MUC4β). The mucin MUC4 is overexpressed in many epithelial malignancies including ovarian cancer, suggesting a possible role in the pathogenesis of these cancers. In this study, we investigated the functional role of MUC4 in the human ovarian cancer cell line SKOV3. The mucin MUC4 was ectopically expressed by stable transfection, and its expression was examined by western blot and confocal microscopy analyses. The in vitro studies demonstrated an enhanced motility of MUC4-expressing SKOV3 cells compared with the vector-transfected cells. The mucin MUC4 expression was associated with apparent changes in actin organisation, leading to the formation of microspike, lammelopodia and filopodia-like cellular projections. An enhanced protein expression and activation of HER2, a receptor tyrosine kinase, was also seen, although no significant change was observed in HER-2 transcript levels in the MUC4-transfected SKOV3 cells. Reciprocal co-immunoprecipitation revealed an interaction of MUC4 with HER2. Further, the MUC4-overexpressing SKOV3 cells exhibited an increase in the phosphorylation of focal adhesion kinase (FAK), Akt and ERK, downstream effectors of HER2. Taken together, our findings demonstrate that MUC4 plays a role in ovarian cancer cell motility, in part, by altering actin arrangement and potentiating HER2 downstream signalling in these cells.
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spelling pubmed-25277932009-09-11 MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells Ponnusamy, M P Singh, A P Jain, M Chakraborty, S Moniaux, N Batra, S K Br J Cancer Molecular Diagnostics The mucin MUC4 is a high molecular weight transmembrane glycoprotein. It consists of a mucin-type subunit (MUC4α) and a transmembrane growth factor-like subunit (MUC4β). The mucin MUC4 is overexpressed in many epithelial malignancies including ovarian cancer, suggesting a possible role in the pathogenesis of these cancers. In this study, we investigated the functional role of MUC4 in the human ovarian cancer cell line SKOV3. The mucin MUC4 was ectopically expressed by stable transfection, and its expression was examined by western blot and confocal microscopy analyses. The in vitro studies demonstrated an enhanced motility of MUC4-expressing SKOV3 cells compared with the vector-transfected cells. The mucin MUC4 expression was associated with apparent changes in actin organisation, leading to the formation of microspike, lammelopodia and filopodia-like cellular projections. An enhanced protein expression and activation of HER2, a receptor tyrosine kinase, was also seen, although no significant change was observed in HER-2 transcript levels in the MUC4-transfected SKOV3 cells. Reciprocal co-immunoprecipitation revealed an interaction of MUC4 with HER2. Further, the MUC4-overexpressing SKOV3 cells exhibited an increase in the phosphorylation of focal adhesion kinase (FAK), Akt and ERK, downstream effectors of HER2. Taken together, our findings demonstrate that MUC4 plays a role in ovarian cancer cell motility, in part, by altering actin arrangement and potentiating HER2 downstream signalling in these cells. Nature Publishing Group 2008-08-05 2008-07-29 /pmc/articles/PMC2527793/ /pubmed/18665193 http://dx.doi.org/10.1038/sj.bjc.6604517 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Ponnusamy, M P
Singh, A P
Jain, M
Chakraborty, S
Moniaux, N
Batra, S K
MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells
title MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells
title_full MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells
title_fullStr MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells
title_full_unstemmed MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells
title_short MUC4 activates HER2 signalling and enhances the motility of human ovarian cancer cells
title_sort muc4 activates her2 signalling and enhances the motility of human ovarian cancer cells
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527793/
https://www.ncbi.nlm.nih.gov/pubmed/18665193
http://dx.doi.org/10.1038/sj.bjc.6604517
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