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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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