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Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity

Centrosome aberrations have been implicated in the development and progression of breast cancer. Our previous worked show that centrosomal protein 70 (Cep70) regulates breast cancer growth and metastasis. However, it remains elusive whether Cep70 is implicated in the sensitivity of the anti-microtub...

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Detalles Bibliográficos
Autores principales: Shi, Xingjuan, Wang, Yujue, Sun, Xiaoou, Wang, Chan, Jiang, Peng, Zhang, Yu, Huang, Qinghai, Liu, Xiangdong, Li, Dengwen, Zhou, Jun, Liu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486089/
https://www.ncbi.nlm.nih.gov/pubmed/28632150
http://dx.doi.org/10.3390/ijms18061267
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author Shi, Xingjuan
Wang, Yujue
Sun, Xiaoou
Wang, Chan
Jiang, Peng
Zhang, Yu
Huang, Qinghai
Liu, Xiangdong
Li, Dengwen
Zhou, Jun
Liu, Min
author_facet Shi, Xingjuan
Wang, Yujue
Sun, Xiaoou
Wang, Chan
Jiang, Peng
Zhang, Yu
Huang, Qinghai
Liu, Xiangdong
Li, Dengwen
Zhou, Jun
Liu, Min
author_sort Shi, Xingjuan
collection PubMed
description Centrosome aberrations have been implicated in the development and progression of breast cancer. Our previous worked show that centrosomal protein 70 (Cep70) regulates breast cancer growth and metastasis. However, it remains elusive whether Cep70 is implicated in the sensitivity of the anti-microtubule drug paclitaxel in breast cancer. Here we provide evidence that Cep70 is a mediator of paclitaxel sensitivity in breast cancer. Cell proliferation assays show that Cep70 expression correlates with paclitaxel sensitivity in breast cancer cell lines. In addition, paclitaxel sensitivity varies when altering Cep70 expression level. Mechanistic studies reveal that Cep70 interacts with tubulin, and promotes the ability of paclitaxel to stimulate microtubule assembly. These data demonstrate that Cep70 mediates paclitaxel sensitivity in breast cancer.
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spelling pubmed-54860892017-06-29 Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity Shi, Xingjuan Wang, Yujue Sun, Xiaoou Wang, Chan Jiang, Peng Zhang, Yu Huang, Qinghai Liu, Xiangdong Li, Dengwen Zhou, Jun Liu, Min Int J Mol Sci Article Centrosome aberrations have been implicated in the development and progression of breast cancer. Our previous worked show that centrosomal protein 70 (Cep70) regulates breast cancer growth and metastasis. However, it remains elusive whether Cep70 is implicated in the sensitivity of the anti-microtubule drug paclitaxel in breast cancer. Here we provide evidence that Cep70 is a mediator of paclitaxel sensitivity in breast cancer. Cell proliferation assays show that Cep70 expression correlates with paclitaxel sensitivity in breast cancer cell lines. In addition, paclitaxel sensitivity varies when altering Cep70 expression level. Mechanistic studies reveal that Cep70 interacts with tubulin, and promotes the ability of paclitaxel to stimulate microtubule assembly. These data demonstrate that Cep70 mediates paclitaxel sensitivity in breast cancer. MDPI 2017-06-20 /pmc/articles/PMC5486089/ /pubmed/28632150 http://dx.doi.org/10.3390/ijms18061267 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shi, Xingjuan
Wang, Yujue
Sun, Xiaoou
Wang, Chan
Jiang, Peng
Zhang, Yu
Huang, Qinghai
Liu, Xiangdong
Li, Dengwen
Zhou, Jun
Liu, Min
Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity
title Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity
title_full Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity
title_fullStr Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity
title_full_unstemmed Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity
title_short Centrosomal Protein 70 Is a Mediator of Paclitaxel Sensitivity
title_sort centrosomal protein 70 is a mediator of paclitaxel sensitivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486089/
https://www.ncbi.nlm.nih.gov/pubmed/28632150
http://dx.doi.org/10.3390/ijms18061267
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