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S100P enhances the motility and invasion of human trophoblast cell lines

S100P has been shown to be a marker for carcinogenesis where its expression in solid tumours correlates with metastasis and a poor patient prognosis. This protein’s role in any physiological process is, however, unknown. Here we first show that S100P is expressed both in trophoblasts in vivo as well...

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Autores principales: Tabrizi, Maral E. A., Lancaster, Tara L., Ismail, Thamir M., Georgiadou, Athina, Ganguly, Ankana, Mistry, Jayna J., Wang, Keqing, Rudland, Philip S., Ahmad, Shakil, Gross, Stephane R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068119/
https://www.ncbi.nlm.nih.gov/pubmed/30065265
http://dx.doi.org/10.1038/s41598-018-29852-2
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author Tabrizi, Maral E. A.
Lancaster, Tara L.
Ismail, Thamir M.
Georgiadou, Athina
Ganguly, Ankana
Mistry, Jayna J.
Wang, Keqing
Rudland, Philip S.
Ahmad, Shakil
Gross, Stephane R.
author_facet Tabrizi, Maral E. A.
Lancaster, Tara L.
Ismail, Thamir M.
Georgiadou, Athina
Ganguly, Ankana
Mistry, Jayna J.
Wang, Keqing
Rudland, Philip S.
Ahmad, Shakil
Gross, Stephane R.
author_sort Tabrizi, Maral E. A.
collection PubMed
description S100P has been shown to be a marker for carcinogenesis where its expression in solid tumours correlates with metastasis and a poor patient prognosis. This protein’s role in any physiological process is, however, unknown. Here we first show that S100P is expressed both in trophoblasts in vivo as well as in some corresponding cell lines in culture. We demonstrate that S100P is predominantly expressed during the early stage of placental formation with its highest expression levels occurring during the first trimester of gestation, particularly in the invading columns and anchoring villi. Using gain or loss of function studies through overexpression or knockdown of S100P expression respectively, our work shows that S100P stimulates both cell motility and cellular invasion in different trophoblastic and first trimester EVT cell lines. Interestingly, cell invasion was seen to be more dramatically affected than cell migration. Our results suggest that S100P may be acting as an important regulator of trophoblast invasion during placentation. This finding sheds new light on a hitherto uncharacterized molecular mechanism which may, in turn, lead to the identification of novel targets that may explain why significant numbers of confirmed human pregnancies suffer complications through poor placental implantation.
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spelling pubmed-60681192018-08-03 S100P enhances the motility and invasion of human trophoblast cell lines Tabrizi, Maral E. A. Lancaster, Tara L. Ismail, Thamir M. Georgiadou, Athina Ganguly, Ankana Mistry, Jayna J. Wang, Keqing Rudland, Philip S. Ahmad, Shakil Gross, Stephane R. Sci Rep Article S100P has been shown to be a marker for carcinogenesis where its expression in solid tumours correlates with metastasis and a poor patient prognosis. This protein’s role in any physiological process is, however, unknown. Here we first show that S100P is expressed both in trophoblasts in vivo as well as in some corresponding cell lines in culture. We demonstrate that S100P is predominantly expressed during the early stage of placental formation with its highest expression levels occurring during the first trimester of gestation, particularly in the invading columns and anchoring villi. Using gain or loss of function studies through overexpression or knockdown of S100P expression respectively, our work shows that S100P stimulates both cell motility and cellular invasion in different trophoblastic and first trimester EVT cell lines. Interestingly, cell invasion was seen to be more dramatically affected than cell migration. Our results suggest that S100P may be acting as an important regulator of trophoblast invasion during placentation. This finding sheds new light on a hitherto uncharacterized molecular mechanism which may, in turn, lead to the identification of novel targets that may explain why significant numbers of confirmed human pregnancies suffer complications through poor placental implantation. Nature Publishing Group UK 2018-07-31 /pmc/articles/PMC6068119/ /pubmed/30065265 http://dx.doi.org/10.1038/s41598-018-29852-2 Text en © The Author(s) 2018 Open Access 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 http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tabrizi, Maral E. A.
Lancaster, Tara L.
Ismail, Thamir M.
Georgiadou, Athina
Ganguly, Ankana
Mistry, Jayna J.
Wang, Keqing
Rudland, Philip S.
Ahmad, Shakil
Gross, Stephane R.
S100P enhances the motility and invasion of human trophoblast cell lines
title S100P enhances the motility and invasion of human trophoblast cell lines
title_full S100P enhances the motility and invasion of human trophoblast cell lines
title_fullStr S100P enhances the motility and invasion of human trophoblast cell lines
title_full_unstemmed S100P enhances the motility and invasion of human trophoblast cell lines
title_short S100P enhances the motility and invasion of human trophoblast cell lines
title_sort s100p enhances the motility and invasion of human trophoblast cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068119/
https://www.ncbi.nlm.nih.gov/pubmed/30065265
http://dx.doi.org/10.1038/s41598-018-29852-2
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