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A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells
BACKGROUND: Cervical cancer is the second most common cancer in females. Recent reports have revealed the critical role of cervical cancer stem cells (CSCs) in tumorigenicity and metastasis. Previously we demonstrated that A1E exerts an anti-proliferative action, which inhibits the growth of cervica...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735966/ https://www.ncbi.nlm.nih.gov/pubmed/26832364 http://dx.doi.org/10.1186/s12906-016-1013-4 |
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author | Kwon, Taeho Bak, Yesol Ham, Sun-Young Yu, Dae-Yeul Yoon, Do-Young |
author_facet | Kwon, Taeho Bak, Yesol Ham, Sun-Young Yu, Dae-Yeul Yoon, Do-Young |
author_sort | Kwon, Taeho |
collection | PubMed |
description | BACKGROUND: Cervical cancer is the second most common cancer in females. Recent reports have revealed the critical role of cervical cancer stem cells (CSCs) in tumorigenicity and metastasis. Previously we demonstrated that A1E exerts an anti-proliferative action, which inhibits the growth of cervical cancer cells. METHODS: A1E is composed of 11 oriental medicinal herbs. Cervical cancer cell culture, wund healing and invasion assay, flow cytometry, sheroid formation assay, and wstern blot assays were performed in HPV 16-positive SiHa cell and HPV 16-negative C33A cells. RESULTS: A1E targets the E6 and E7 oncogenes; thus, A1E significantly inhibited proliferation of human papilloma virus (HPV) 16-positive SiHa cells, it did not inhibit the proliferation of HPV-negative C33A cells. Accordingly, we investigated whether A1E can regulate epithelial-to-mesenchymal transition (EMT), CSC self-renewal, and stemness-related gene expression in cervical cancer cells. Down rgulation of cell migration, cell invasion, and EMT was observed in A1E-treated SiHa cells. Specifically, A1E-treated SiHa cells showed significant decreases in OCT-3/4 and Sox2 expression levels and in sphere formation. Moreover, CSCs makers ALDH+ and ALDH, CD133 double positive cell were significantly decreased in A1E-treated SiHa cells. However, A1E treatment did not down regulate ALDH+ expression and the number of ALDH/CD133 double positive cells in C33A cells. CONCLUSIONS: Taken together, A1E can inhibit CSCs and reduce the expression of stemness markers. Treating CSCs with A1E may be a potential therapy for cervical cancer. |
format | Online Article Text |
id | pubmed-4735966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47359662016-02-03 A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells Kwon, Taeho Bak, Yesol Ham, Sun-Young Yu, Dae-Yeul Yoon, Do-Young BMC Complement Altern Med Research Article BACKGROUND: Cervical cancer is the second most common cancer in females. Recent reports have revealed the critical role of cervical cancer stem cells (CSCs) in tumorigenicity and metastasis. Previously we demonstrated that A1E exerts an anti-proliferative action, which inhibits the growth of cervical cancer cells. METHODS: A1E is composed of 11 oriental medicinal herbs. Cervical cancer cell culture, wund healing and invasion assay, flow cytometry, sheroid formation assay, and wstern blot assays were performed in HPV 16-positive SiHa cell and HPV 16-negative C33A cells. RESULTS: A1E targets the E6 and E7 oncogenes; thus, A1E significantly inhibited proliferation of human papilloma virus (HPV) 16-positive SiHa cells, it did not inhibit the proliferation of HPV-negative C33A cells. Accordingly, we investigated whether A1E can regulate epithelial-to-mesenchymal transition (EMT), CSC self-renewal, and stemness-related gene expression in cervical cancer cells. Down rgulation of cell migration, cell invasion, and EMT was observed in A1E-treated SiHa cells. Specifically, A1E-treated SiHa cells showed significant decreases in OCT-3/4 and Sox2 expression levels and in sphere formation. Moreover, CSCs makers ALDH+ and ALDH, CD133 double positive cell were significantly decreased in A1E-treated SiHa cells. However, A1E treatment did not down regulate ALDH+ expression and the number of ALDH/CD133 double positive cells in C33A cells. CONCLUSIONS: Taken together, A1E can inhibit CSCs and reduce the expression of stemness markers. Treating CSCs with A1E may be a potential therapy for cervical cancer. BioMed Central 2016-02-02 /pmc/articles/PMC4735966/ /pubmed/26832364 http://dx.doi.org/10.1186/s12906-016-1013-4 Text en © Kwon et al. 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 Article Kwon, Taeho Bak, Yesol Ham, Sun-Young Yu, Dae-Yeul Yoon, Do-Young A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells |
title | A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells |
title_full | A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells |
title_fullStr | A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells |
title_full_unstemmed | A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells |
title_short | A1E reduces stemness and self-renewal in HPV 16-positive cervical cancer stem cells |
title_sort | a1e reduces stemness and self-renewal in hpv 16-positive cervical cancer stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735966/ https://www.ncbi.nlm.nih.gov/pubmed/26832364 http://dx.doi.org/10.1186/s12906-016-1013-4 |
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