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PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells
Purkinje cell protein (PCP) 4/peptide (PEP) 19 is expressed in Purkinje cells where it has a calmodulin-binding, anti-apoptotic function. We recently demonstrated that PCP4/PEP19 is expressed and inhibit apoptosis in human breast cancer cell lines. In the present study we investigated the role of PC...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226490/ https://www.ncbi.nlm.nih.gov/pubmed/27384474 http://dx.doi.org/10.18632/oncotarget.7529 |
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author | Yoshimura, Takuya Hamada, Taiji Hijioka, Hiroshi Souda, Masakazu Hatanaka, Kazuhito Yoshioka, Takako Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Nakamura, Norifumi Tanimoto, Akihide |
author_facet | Yoshimura, Takuya Hamada, Taiji Hijioka, Hiroshi Souda, Masakazu Hatanaka, Kazuhito Yoshioka, Takako Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Nakamura, Norifumi Tanimoto, Akihide |
author_sort | Yoshimura, Takuya |
collection | PubMed |
description | Purkinje cell protein (PCP) 4/peptide (PEP) 19 is expressed in Purkinje cells where it has a calmodulin-binding, anti-apoptotic function. We recently demonstrated that PCP4/PEP19 is expressed and inhibit apoptosis in human breast cancer cell lines. In the present study we investigated the role of PCP4/PEP19 in cell morphology, adhesion, migration, and invasion in MCF-7 and T47D human breast cancer cell lines. Knockdown of PCP4/PEP19 reduced the formation of filopodia-like cytoplasmic structures and vinculin expression, and enhanced E-cadherin expression. Activities of migration, invasion, and cell adhesion were also decreased after the knockdown of PCP4/PEP19 in MCF-7 and T47D cells. These results suggested that PCP4/PEP19 promotes cancer cell adhesion, migration, and invasion and that PCP4/PEP19 may be a potential target for therapeutic agents in breast cancer treatment which act by inhibiting epithelial-mesenchymal transition and enhancing apoptotic cell death. |
format | Online Article Text |
id | pubmed-5226490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52264902017-01-18 PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells Yoshimura, Takuya Hamada, Taiji Hijioka, Hiroshi Souda, Masakazu Hatanaka, Kazuhito Yoshioka, Takako Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Nakamura, Norifumi Tanimoto, Akihide Oncotarget Research Paper Purkinje cell protein (PCP) 4/peptide (PEP) 19 is expressed in Purkinje cells where it has a calmodulin-binding, anti-apoptotic function. We recently demonstrated that PCP4/PEP19 is expressed and inhibit apoptosis in human breast cancer cell lines. In the present study we investigated the role of PCP4/PEP19 in cell morphology, adhesion, migration, and invasion in MCF-7 and T47D human breast cancer cell lines. Knockdown of PCP4/PEP19 reduced the formation of filopodia-like cytoplasmic structures and vinculin expression, and enhanced E-cadherin expression. Activities of migration, invasion, and cell adhesion were also decreased after the knockdown of PCP4/PEP19 in MCF-7 and T47D cells. These results suggested that PCP4/PEP19 promotes cancer cell adhesion, migration, and invasion and that PCP4/PEP19 may be a potential target for therapeutic agents in breast cancer treatment which act by inhibiting epithelial-mesenchymal transition and enhancing apoptotic cell death. Impact Journals LLC 2016-02-20 /pmc/articles/PMC5226490/ /pubmed/27384474 http://dx.doi.org/10.18632/oncotarget.7529 Text en Copyright: © 2016 Yoshimura 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 Yoshimura, Takuya Hamada, Taiji Hijioka, Hiroshi Souda, Masakazu Hatanaka, Kazuhito Yoshioka, Takako Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Nakamura, Norifumi Tanimoto, Akihide PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells |
title | PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells |
title_full | PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells |
title_fullStr | PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells |
title_full_unstemmed | PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells |
title_short | PCP4/PEP19 promotes migration, invasion and adhesion in human breast cancer MCF-7 and T47D cells |
title_sort | pcp4/pep19 promotes migration, invasion and adhesion in human breast cancer mcf-7 and t47d cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226490/ https://www.ncbi.nlm.nih.gov/pubmed/27384474 http://dx.doi.org/10.18632/oncotarget.7529 |
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