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MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression
Paclitaxel (Taxol) is an effective chemotherapeutic agent for treating breast cancer patients. However, chemoresistance is a major obstacle in cancer treatment. Here, we showed that overexpression of miR-16 promoted Taxol-induced cytotoxicity and apoptosis in breast cancer cells. Furthermore, IκB ki...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029655/ https://www.ncbi.nlm.nih.gov/pubmed/26993770 http://dx.doi.org/10.18632/oncotarget.8056 |
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author | Tang, Xueyuan Jin, Long Cao, Peiguo Cao, Ke Huang, Chenghui Luo, Yanwei Ma, Jian Shen, Shourong Tan, Ming Li, Xiayu Zhou, Ming |
author_facet | Tang, Xueyuan Jin, Long Cao, Peiguo Cao, Ke Huang, Chenghui Luo, Yanwei Ma, Jian Shen, Shourong Tan, Ming Li, Xiayu Zhou, Ming |
author_sort | Tang, Xueyuan |
collection | PubMed |
description | Paclitaxel (Taxol) is an effective chemotherapeutic agent for treating breast cancer patients. However, chemoresistance is a major obstacle in cancer treatment. Here, we showed that overexpression of miR-16 promoted Taxol-induced cytotoxicity and apoptosis in breast cancer cells. Furthermore, IκB kinase β (IKBKB) was identified as a direct target of miR-16. Up-regulation of IKBKB suppressed Taxol-induced apoptosis and led to an increased resistance to Taxol, and restoring IKBKB expression in miR-16-overexpressing breast cancer cells recovered Taxol resistance. Moreover, miR-16 was highly expressed in Taxol-sensitive breast cancer tissues compared with Taxol-resistant tissues, and there was an inverse correlation between miR-16 expression and IKBKB expression in breast cancer tissues. The expression levels of miR-16 were negatively associated with T stages, whereas the expression of IKBKB was positively correlated with T stages, lymph node metastasis and clinical stages. Taken together, our data demonstrates that miR-16 sensitizes breast cancer cells to Taxol through the suppression of IKBKB expression, and targeting miR-16/IKBKB axis will be a promising strategy for overcoming Taxol resistance in breast cancer. |
format | Online Article Text |
id | pubmed-5029655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50296552016-09-29 MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression Tang, Xueyuan Jin, Long Cao, Peiguo Cao, Ke Huang, Chenghui Luo, Yanwei Ma, Jian Shen, Shourong Tan, Ming Li, Xiayu Zhou, Ming Oncotarget Research Paper Paclitaxel (Taxol) is an effective chemotherapeutic agent for treating breast cancer patients. However, chemoresistance is a major obstacle in cancer treatment. Here, we showed that overexpression of miR-16 promoted Taxol-induced cytotoxicity and apoptosis in breast cancer cells. Furthermore, IκB kinase β (IKBKB) was identified as a direct target of miR-16. Up-regulation of IKBKB suppressed Taxol-induced apoptosis and led to an increased resistance to Taxol, and restoring IKBKB expression in miR-16-overexpressing breast cancer cells recovered Taxol resistance. Moreover, miR-16 was highly expressed in Taxol-sensitive breast cancer tissues compared with Taxol-resistant tissues, and there was an inverse correlation between miR-16 expression and IKBKB expression in breast cancer tissues. The expression levels of miR-16 were negatively associated with T stages, whereas the expression of IKBKB was positively correlated with T stages, lymph node metastasis and clinical stages. Taken together, our data demonstrates that miR-16 sensitizes breast cancer cells to Taxol through the suppression of IKBKB expression, and targeting miR-16/IKBKB axis will be a promising strategy for overcoming Taxol resistance in breast cancer. Impact Journals LLC 2016-03-14 /pmc/articles/PMC5029655/ /pubmed/26993770 http://dx.doi.org/10.18632/oncotarget.8056 Text en Copyright: © 2016 Tang et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Tang, Xueyuan Jin, Long Cao, Peiguo Cao, Ke Huang, Chenghui Luo, Yanwei Ma, Jian Shen, Shourong Tan, Ming Li, Xiayu Zhou, Ming MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression |
title | MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression |
title_full | MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression |
title_fullStr | MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression |
title_full_unstemmed | MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression |
title_short | MicroRNA-16 sensitizes breast cancer cells to paclitaxel through suppression of IKBKB expression |
title_sort | microrna-16 sensitizes breast cancer cells to paclitaxel through suppression of ikbkb expression |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029655/ https://www.ncbi.nlm.nih.gov/pubmed/26993770 http://dx.doi.org/10.18632/oncotarget.8056 |
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