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Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p
BACKGROUND: Cancer incidence and mortality have been increasing in China, making cancer the leading cause of death since 2010 and a major public health concern in the country. Cancer stem cells have been studied in relation to the treatment of different malignancies, including gastric cancer. Antica...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034486/ https://www.ncbi.nlm.nih.gov/pubmed/27688872 http://dx.doi.org/10.1186/s13578-016-0112-8 |
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author | Xing, Zhiwei Yu, Lan Li, Xian Su, Xiulan |
author_facet | Xing, Zhiwei Yu, Lan Li, Xian Su, Xiulan |
author_sort | Xing, Zhiwei |
collection | PubMed |
description | BACKGROUND: Cancer incidence and mortality have been increasing in China, making cancer the leading cause of death since 2010 and a major public health concern in the country. Cancer stem cells have been studied in relation to the treatment of different malignancies, including gastric cancer. Anticancer bioactive peptide-3 (ACBP-3) can induce the apoptosis of gastric cancer stem cells (GCSCs) and reduce their tumorigenicity. In the present study, for the first time, we used a miRNA microarray and bioinformatics analysis to identify differentially expressed miRNAs in ACBP-3-treated GCSCs and GCSC-derived tumors in a xenograft model and functionally verified the identified miRNAs. miR-338-5p was selected based on its significant upregulation by ACBP-3 both in cultured GCSCs and in tumor tissues. RESULTS: miR-338-5p was downregulated in GCSCs compared with normal gastric epithelial cells, and the ectopic restoration of miR-338-5p expression in GCSCs inhibited cell proliferation and induced apoptosis, which correlated with the upregulation of the pro-apoptotic Bcl-2 proteins BAK and BIM. We also found that ACBP-3-treated GCSCs could respond to lower effective doses of cisplatin (DDP) or 5-fluorouracil (5-FU), possibly because ACBP-3 induced the expression of miR-338-5p and the BAK and BIM proteins and promoted GCSC apoptosis. CONCLUSIONS: Our data indicate that miR-338-5p is part of an important pathway for the inhibition of human gastric cancer stem cell proliferation by ACBP-3 combined with chemotherapeutics. ACBP-3 could suppress GCSC proliferation and lower the required effective dose of cisplatin or 5-fluorouracil. Therefore, this study provides not only further evidence for the remarkable anti-tumor effect of ACBP-3 but also a possible new approach for the development of GCSC-targeting therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13578-016-0112-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5034486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50344862016-09-29 Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p Xing, Zhiwei Yu, Lan Li, Xian Su, Xiulan Cell Biosci Research BACKGROUND: Cancer incidence and mortality have been increasing in China, making cancer the leading cause of death since 2010 and a major public health concern in the country. Cancer stem cells have been studied in relation to the treatment of different malignancies, including gastric cancer. Anticancer bioactive peptide-3 (ACBP-3) can induce the apoptosis of gastric cancer stem cells (GCSCs) and reduce their tumorigenicity. In the present study, for the first time, we used a miRNA microarray and bioinformatics analysis to identify differentially expressed miRNAs in ACBP-3-treated GCSCs and GCSC-derived tumors in a xenograft model and functionally verified the identified miRNAs. miR-338-5p was selected based on its significant upregulation by ACBP-3 both in cultured GCSCs and in tumor tissues. RESULTS: miR-338-5p was downregulated in GCSCs compared with normal gastric epithelial cells, and the ectopic restoration of miR-338-5p expression in GCSCs inhibited cell proliferation and induced apoptosis, which correlated with the upregulation of the pro-apoptotic Bcl-2 proteins BAK and BIM. We also found that ACBP-3-treated GCSCs could respond to lower effective doses of cisplatin (DDP) or 5-fluorouracil (5-FU), possibly because ACBP-3 induced the expression of miR-338-5p and the BAK and BIM proteins and promoted GCSC apoptosis. CONCLUSIONS: Our data indicate that miR-338-5p is part of an important pathway for the inhibition of human gastric cancer stem cell proliferation by ACBP-3 combined with chemotherapeutics. ACBP-3 could suppress GCSC proliferation and lower the required effective dose of cisplatin or 5-fluorouracil. Therefore, this study provides not only further evidence for the remarkable anti-tumor effect of ACBP-3 but also a possible new approach for the development of GCSC-targeting therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13578-016-0112-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-22 /pmc/articles/PMC5034486/ /pubmed/27688872 http://dx.doi.org/10.1186/s13578-016-0112-8 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Xing, Zhiwei Yu, Lan Li, Xian Su, Xiulan Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p |
title | Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p |
title_full | Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p |
title_fullStr | Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p |
title_full_unstemmed | Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p |
title_short | Anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting miR-338-5p |
title_sort | anticancer bioactive peptide-3 inhibits human gastric cancer growth by targeting mir-338-5p |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034486/ https://www.ncbi.nlm.nih.gov/pubmed/27688872 http://dx.doi.org/10.1186/s13578-016-0112-8 |
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