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Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells
The development of chemoresistance and inability in elimination of cancer stem cells are among the key limitations of cancer chemotherapy. Novel molecular therapeutic strategies able to overcome such limitations are urgently needed for future effective management of cancer. In this report, we show t...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517644/ https://www.ncbi.nlm.nih.gov/pubmed/28724889 http://dx.doi.org/10.1038/s41598-017-05859-z |
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author | AlShamaileh, Hadi Wang, Tao Xiang, Dongxi Yin, Wang Tran, Phuong Ha-Lien Barrero, Roberto A. Zhang, Pei-Zhuo Li, Yong Kong, Lingxue Liu, Ke Zhou, Shu-Feng Hou, Yingchun Shigdar, Sarah Duan, Wei |
author_facet | AlShamaileh, Hadi Wang, Tao Xiang, Dongxi Yin, Wang Tran, Phuong Ha-Lien Barrero, Roberto A. Zhang, Pei-Zhuo Li, Yong Kong, Lingxue Liu, Ke Zhou, Shu-Feng Hou, Yingchun Shigdar, Sarah Duan, Wei |
author_sort | AlShamaileh, Hadi |
collection | PubMed |
description | The development of chemoresistance and inability in elimination of cancer stem cells are among the key limitations of cancer chemotherapy. Novel molecular therapeutic strategies able to overcome such limitations are urgently needed for future effective management of cancer. In this report, we show that EpCAM-aptamer-guided survivin RNAi effectively downregulated survivin both in colorectal cancer cells in vitro and in a mouse xenograft model for colorectal cancer. When combined with the conventional chemotherapeutic agents, the aptamer-guided survivin RNAi was able to enhance the sensitivity towards 5-FU or oxaliplatin in colorectal cancer stem cells, increase apoptosis, inhibit tumour growth and improve the overall survival of mice bearing xenograft colorectal cancer. Our results indicate that survivin is one of the key players responsible for the innate chemoresistance of colorectal cancer stem cells. Thus, aptamer-mediated targeting of survivin in cancer stem cells in combination with chemotherapeutic drugs constitutes a new avenue to improve treatment outcome in oncologic clinics. |
format | Online Article Text |
id | pubmed-5517644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55176442017-07-20 Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells AlShamaileh, Hadi Wang, Tao Xiang, Dongxi Yin, Wang Tran, Phuong Ha-Lien Barrero, Roberto A. Zhang, Pei-Zhuo Li, Yong Kong, Lingxue Liu, Ke Zhou, Shu-Feng Hou, Yingchun Shigdar, Sarah Duan, Wei Sci Rep Article The development of chemoresistance and inability in elimination of cancer stem cells are among the key limitations of cancer chemotherapy. Novel molecular therapeutic strategies able to overcome such limitations are urgently needed for future effective management of cancer. In this report, we show that EpCAM-aptamer-guided survivin RNAi effectively downregulated survivin both in colorectal cancer cells in vitro and in a mouse xenograft model for colorectal cancer. When combined with the conventional chemotherapeutic agents, the aptamer-guided survivin RNAi was able to enhance the sensitivity towards 5-FU or oxaliplatin in colorectal cancer stem cells, increase apoptosis, inhibit tumour growth and improve the overall survival of mice bearing xenograft colorectal cancer. Our results indicate that survivin is one of the key players responsible for the innate chemoresistance of colorectal cancer stem cells. Thus, aptamer-mediated targeting of survivin in cancer stem cells in combination with chemotherapeutic drugs constitutes a new avenue to improve treatment outcome in oncologic clinics. Nature Publishing Group UK 2017-07-19 /pmc/articles/PMC5517644/ /pubmed/28724889 http://dx.doi.org/10.1038/s41598-017-05859-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article AlShamaileh, Hadi Wang, Tao Xiang, Dongxi Yin, Wang Tran, Phuong Ha-Lien Barrero, Roberto A. Zhang, Pei-Zhuo Li, Yong Kong, Lingxue Liu, Ke Zhou, Shu-Feng Hou, Yingchun Shigdar, Sarah Duan, Wei Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells |
title | Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells |
title_full | Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells |
title_fullStr | Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells |
title_full_unstemmed | Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells |
title_short | Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells |
title_sort | aptamer-mediated survivin rnai enables 5-fluorouracil to eliminate colorectal cancer stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517644/ https://www.ncbi.nlm.nih.gov/pubmed/28724889 http://dx.doi.org/10.1038/s41598-017-05859-z |
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