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PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells
The Purkinje cell protein 4/peptide 19 (PCP4/PEP19) is a novel breast cancer cell expressing peptide, originally found in the neural cells as an anti-apoptotic factor, could inhibit cell apoptosis and enhance cell migration and invasion in human breast cancer cell lines. The expression of PCP4/PEP19...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6049867/ https://www.ncbi.nlm.nih.gov/pubmed/30038708 http://dx.doi.org/10.18632/oncotarget.25651 |
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author | Honjo, Kie Hamada, Taiji Yoshimura, Takuya Yokoyama, Seiya Yamada, Sohsuke Tan, Yan-Qin Leung, Lai K. Nakamura, Norifumi Ohi, Yasuyo Higashi, Michiyo Tanimoto, Akihide |
author_facet | Honjo, Kie Hamada, Taiji Yoshimura, Takuya Yokoyama, Seiya Yamada, Sohsuke Tan, Yan-Qin Leung, Lai K. Nakamura, Norifumi Ohi, Yasuyo Higashi, Michiyo Tanimoto, Akihide |
author_sort | Honjo, Kie |
collection | PubMed |
description | The Purkinje cell protein 4/peptide 19 (PCP4/PEP19) is a novel breast cancer cell expressing peptide, originally found in the neural cells as an anti-apoptotic factor, could inhibit cell apoptosis and enhance cell migration and invasion in human breast cancer cell lines. The expression of PCP4/PEP19 is induced by estrogens in estrogen receptor-positive (ER(+)) MCF-7 cells but also highly expressed in ER(-) SK-BR-3 cells. In this study, we investigated the effects of PCP4/PEP19 on aromatase gene expression in MCF-7 and SK-BR-3 human breast cancer cells. In SK-BR-3 cells but not in MCF-7 cells, PCP4/PEP19 knockdown by siRNA silencing decreased the aromatase expression in gene transcriptional level. When PCP4/PEP19 was overexpressed by CMV promoter-driven PCP4/PEP19 expressing plasmid transfection, aromatase gene transcription increased in SK-BR-3 cells. This aromatase gene transcription is mainly mediated through promoter region PI.1, which is usually active in the placental tissue but not in the breast cancer tissue. These results indicate a new function of PCP4/PEP19 that would enhance aromatase gene upregulation to supply estrogens in heterogeneous cancer microenvironment. |
format | Online Article Text |
id | pubmed-6049867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-60498672018-07-23 PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells Honjo, Kie Hamada, Taiji Yoshimura, Takuya Yokoyama, Seiya Yamada, Sohsuke Tan, Yan-Qin Leung, Lai K. Nakamura, Norifumi Ohi, Yasuyo Higashi, Michiyo Tanimoto, Akihide Oncotarget Research Paper The Purkinje cell protein 4/peptide 19 (PCP4/PEP19) is a novel breast cancer cell expressing peptide, originally found in the neural cells as an anti-apoptotic factor, could inhibit cell apoptosis and enhance cell migration and invasion in human breast cancer cell lines. The expression of PCP4/PEP19 is induced by estrogens in estrogen receptor-positive (ER(+)) MCF-7 cells but also highly expressed in ER(-) SK-BR-3 cells. In this study, we investigated the effects of PCP4/PEP19 on aromatase gene expression in MCF-7 and SK-BR-3 human breast cancer cells. In SK-BR-3 cells but not in MCF-7 cells, PCP4/PEP19 knockdown by siRNA silencing decreased the aromatase expression in gene transcriptional level. When PCP4/PEP19 was overexpressed by CMV promoter-driven PCP4/PEP19 expressing plasmid transfection, aromatase gene transcription increased in SK-BR-3 cells. This aromatase gene transcription is mainly mediated through promoter region PI.1, which is usually active in the placental tissue but not in the breast cancer tissue. These results indicate a new function of PCP4/PEP19 that would enhance aromatase gene upregulation to supply estrogens in heterogeneous cancer microenvironment. Impact Journals LLC 2018-07-03 /pmc/articles/PMC6049867/ /pubmed/30038708 http://dx.doi.org/10.18632/oncotarget.25651 Text en Copyright: © 2018 Honjo et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Honjo, Kie Hamada, Taiji Yoshimura, Takuya Yokoyama, Seiya Yamada, Sohsuke Tan, Yan-Qin Leung, Lai K. Nakamura, Norifumi Ohi, Yasuyo Higashi, Michiyo Tanimoto, Akihide PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells |
title | PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells |
title_full | PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells |
title_fullStr | PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells |
title_full_unstemmed | PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells |
title_short | PCP4/PEP19 upregulates aromatase gene expression via CYP19A1 promoter I.1 in human breast cancer SK-BR-3 cells |
title_sort | pcp4/pep19 upregulates aromatase gene expression via cyp19a1 promoter i.1 in human breast cancer sk-br-3 cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6049867/ https://www.ncbi.nlm.nih.gov/pubmed/30038708 http://dx.doi.org/10.18632/oncotarget.25651 |
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