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Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget
The PCP4/PEP19 is a calmodulin-binding anti-apoptotic peptide in neural cells but its potential role in human cancer has largely been unknown. We investigated the expression of PCP4/PEP19 in human breast cancer cell lines MCF-7, SK-BR-3, and MDA-MB-231 cells, and found that estrogen receptor (ER)-po...
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/PMC4171614/ https://www.ncbi.nlm.nih.gov/pubmed/25153723 |
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author | Hamada, Taiji Souda, Masakazu Yoshimura, Takuya Sasaguri, Shoko Hatanaka, Kazuhito Tasaki, Takashi Yoshioka, Takako Ohi, Yasuyo Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Tanimoto, Akihide |
author_facet | Hamada, Taiji Souda, Masakazu Yoshimura, Takuya Sasaguri, Shoko Hatanaka, Kazuhito Tasaki, Takashi Yoshioka, Takako Ohi, Yasuyo Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Tanimoto, Akihide |
author_sort | Hamada, Taiji |
collection | PubMed |
description | The PCP4/PEP19 is a calmodulin-binding anti-apoptotic peptide in neural cells but its potential role in human cancer has largely been unknown. We investigated the expression of PCP4/PEP19 in human breast cancer cell lines MCF-7, SK-BR-3, and MDA-MB-231 cells, and found that estrogen receptor (ER)-positive MCF-7 and ER-negative SK-BR-3 cells expressed PCP4/PEP19. In the MCF-7 cells, cell proliferation was estrogen-dependent, and PCP4/PEP19 expression was induced by estrogen. In both cell lines, PCP4/PEP19 knockdown induced apoptosis and slightly decreased Akt phosphorylation. Knockdown of calcium/calmodulin-dependent protein kinase kinase 1 (CaMKK1), resulting in decreased phospho-Akt(Thr308), enhanced apoptosis in SK-BR-3 but not in MCF-7 cells. CaMKK2 knockdown moderately decreased phospho-Akt(Thr308) and increased apoptosis in MCF-7 cells but not in SK-BR-3 cells. These data indicated that PCP4/PEP19 regulates apoptosis but exact mechanism is still unknown. PCP4/PEP19 can therefore potentially serve as independent oncotarget for therapy of PCP4/PEP19-positive breast cancers irrespective of ER expression. |
format | Online Article Text |
id | pubmed-4171614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41716142014-09-23 Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget Hamada, Taiji Souda, Masakazu Yoshimura, Takuya Sasaguri, Shoko Hatanaka, Kazuhito Tasaki, Takashi Yoshioka, Takako Ohi, Yasuyo Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Tanimoto, Akihide Oncotarget Research Paper The PCP4/PEP19 is a calmodulin-binding anti-apoptotic peptide in neural cells but its potential role in human cancer has largely been unknown. We investigated the expression of PCP4/PEP19 in human breast cancer cell lines MCF-7, SK-BR-3, and MDA-MB-231 cells, and found that estrogen receptor (ER)-positive MCF-7 and ER-negative SK-BR-3 cells expressed PCP4/PEP19. In the MCF-7 cells, cell proliferation was estrogen-dependent, and PCP4/PEP19 expression was induced by estrogen. In both cell lines, PCP4/PEP19 knockdown induced apoptosis and slightly decreased Akt phosphorylation. Knockdown of calcium/calmodulin-dependent protein kinase kinase 1 (CaMKK1), resulting in decreased phospho-Akt(Thr308), enhanced apoptosis in SK-BR-3 but not in MCF-7 cells. CaMKK2 knockdown moderately decreased phospho-Akt(Thr308) and increased apoptosis in MCF-7 cells but not in SK-BR-3 cells. These data indicated that PCP4/PEP19 regulates apoptosis but exact mechanism is still unknown. PCP4/PEP19 can therefore potentially serve as independent oncotarget for therapy of PCP4/PEP19-positive breast cancers irrespective of ER expression. Impact Journals LLC 2014-07-08 /pmc/articles/PMC4171614/ /pubmed/25153723 Text en Copyright: © 2014 Hamada 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 Hamada, Taiji Souda, Masakazu Yoshimura, Takuya Sasaguri, Shoko Hatanaka, Kazuhito Tasaki, Takashi Yoshioka, Takako Ohi, Yasuyo Yamada, Sohsuke Tsutsui, Masato Umekita, Yoshihisa Tanimoto, Akihide Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget |
title | Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget |
title_full | Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget |
title_fullStr | Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget |
title_full_unstemmed | Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget |
title_short | Anti-apoptotic Effects of PCP4/PEP19 in Human Breast Cancer Cell Lines: A Novel Oncotarget |
title_sort | anti-apoptotic effects of pcp4/pep19 in human breast cancer cell lines: a novel oncotarget |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171614/ https://www.ncbi.nlm.nih.gov/pubmed/25153723 |
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