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The role of S100A14 in epithelial ovarian tumors
S100A14 is an EF-hand calcium-binding protein that has been reported to be involved in the progression of many malignancies. However, its role in ovarian cancer has not yet been clarified. In this study, we investigated the significance of S100A14 expression in epithelial ovarian cancers (EOCs) as w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116497/ https://www.ncbi.nlm.nih.gov/pubmed/24939856 |
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author | Cho, Hanbyoul Shin, Ha-Yeon Kim, Sunghoon Kim, Jane Seon-Young Chung, Joon-Yong Chung, Eun Joo Chun, Kyung-Hee Hewitt, Stephen M. Kim, Jae-Hoon |
author_facet | Cho, Hanbyoul Shin, Ha-Yeon Kim, Sunghoon Kim, Jane Seon-Young Chung, Joon-Yong Chung, Eun Joo Chun, Kyung-Hee Hewitt, Stephen M. Kim, Jae-Hoon |
author_sort | Cho, Hanbyoul |
collection | PubMed |
description | S100A14 is an EF-hand calcium-binding protein that has been reported to be involved in the progression of many malignancies. However, its role in ovarian cancer has not yet been clarified. In this study, we investigated the significance of S100A14 expression in epithelial ovarian cancers (EOCs) as well as it's mechanism of action. On both RNA and protein levels, S100A14 was overexpressed in transformed cells. Immunohistochemical staining demonstrated that S100A14 expression was associated with advanced stage (P < 0.001) and poor tumor grade (P < 0.001). Moreover, S100A14 overexpression was an independent prognostic factor for overall survival (HR = 4.53, P = 0.029). We also investigated S100A14's functional role by employing lentiviral-mediated overexpression and knockdown in EOC cells. S100A14 overexpression promoted cell proliferation, tumorigenesis, migration, and invasion, whereas S100A14 knockdown inhibited these properties. TOV112D cells that overexpressed S100A14 also exhibited greater tumor growth potential in xenografted mice. S100A14 promoted such a malignant phenotype in EOC cells through the PI3K/Akt pathway. Taken together, our data indicate that S100A14 has a crucial role in EOC progression, and its overexpression is associated with poor prognosis. Further study of S100A14's molecular mechanisms may lead to the development of a novel therapeutic target for ovarian cancer. |
format | Online Article Text |
id | pubmed-4116497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41164972014-08-04 The role of S100A14 in epithelial ovarian tumors Cho, Hanbyoul Shin, Ha-Yeon Kim, Sunghoon Kim, Jane Seon-Young Chung, Joon-Yong Chung, Eun Joo Chun, Kyung-Hee Hewitt, Stephen M. Kim, Jae-Hoon Oncotarget Research Paper S100A14 is an EF-hand calcium-binding protein that has been reported to be involved in the progression of many malignancies. However, its role in ovarian cancer has not yet been clarified. In this study, we investigated the significance of S100A14 expression in epithelial ovarian cancers (EOCs) as well as it's mechanism of action. On both RNA and protein levels, S100A14 was overexpressed in transformed cells. Immunohistochemical staining demonstrated that S100A14 expression was associated with advanced stage (P < 0.001) and poor tumor grade (P < 0.001). Moreover, S100A14 overexpression was an independent prognostic factor for overall survival (HR = 4.53, P = 0.029). We also investigated S100A14's functional role by employing lentiviral-mediated overexpression and knockdown in EOC cells. S100A14 overexpression promoted cell proliferation, tumorigenesis, migration, and invasion, whereas S100A14 knockdown inhibited these properties. TOV112D cells that overexpressed S100A14 also exhibited greater tumor growth potential in xenografted mice. S100A14 promoted such a malignant phenotype in EOC cells through the PI3K/Akt pathway. Taken together, our data indicate that S100A14 has a crucial role in EOC progression, and its overexpression is associated with poor prognosis. Further study of S100A14's molecular mechanisms may lead to the development of a novel therapeutic target for ovarian cancer. Impact Journals LLC 2014-05-06 /pmc/articles/PMC4116497/ /pubmed/24939856 Text en Copyright: © 2014 Cho et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Cho, Hanbyoul Shin, Ha-Yeon Kim, Sunghoon Kim, Jane Seon-Young Chung, Joon-Yong Chung, Eun Joo Chun, Kyung-Hee Hewitt, Stephen M. Kim, Jae-Hoon The role of S100A14 in epithelial ovarian tumors |
title | The role of S100A14 in epithelial ovarian tumors |
title_full | The role of S100A14 in epithelial ovarian tumors |
title_fullStr | The role of S100A14 in epithelial ovarian tumors |
title_full_unstemmed | The role of S100A14 in epithelial ovarian tumors |
title_short | The role of S100A14 in epithelial ovarian tumors |
title_sort | role of s100a14 in epithelial ovarian tumors |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116497/ https://www.ncbi.nlm.nih.gov/pubmed/24939856 |
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