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Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration
The microtubule (MT) plus-end binding protein Clip170 is associated closely with breast cancer invasion and migration. In this study, Clip170 tension observed by a newly designed cpstFRET tension probe was suggested to be positive related to breast cancer aggressiveness, which could be regulated by...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9547975/ https://www.ncbi.nlm.nih.gov/pubmed/36209218 http://dx.doi.org/10.1038/s41419-022-05306-6 |
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author | Hu, Yunfeng Xie, Qiu Wu, Xiang Liu, Weizhen Li, DongFang Li, Chen Zhao, WangXing Chen, LinLin Zheng, Zihui Li, GuangMing Guo, Jun |
author_facet | Hu, Yunfeng Xie, Qiu Wu, Xiang Liu, Weizhen Li, DongFang Li, Chen Zhao, WangXing Chen, LinLin Zheng, Zihui Li, GuangMing Guo, Jun |
author_sort | Hu, Yunfeng |
collection | PubMed |
description | The microtubule (MT) plus-end binding protein Clip170 is associated closely with breast cancer invasion and migration. In this study, Clip170 tension observed by a newly designed cpstFRET tension probe was suggested to be positive related to breast cancer aggressiveness, which could be regulated by α-tubulin detyrosination-induced MT disassembly. Clip170 phosphorylation induced by Ribosomal protein S6 kinase (RSK) could also increase its tension and promote the conversion of a discrete comet-like Clip-170 distribution into a spotty pattern during cancer metastasis. Heightened Clip170 tension was correlated with the formation of cortactin-associated filopodia and lamellipodia, and then promoted invasion and metastasis both in vitro and in vivo. Meanwhile, Clip170 tension enhanced at the leading edge in directional migration, accompanying with IQGAP1 subcellular distribution variation. Our work indicates that the malignancy and directionality during breast cancer migration depend on the magnitude and polarization of Clip170 tension, and we suggest Clip170 tension as a new potential drug target for breast cancer therapy. |
format | Online Article Text |
id | pubmed-9547975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95479752022-10-10 Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration Hu, Yunfeng Xie, Qiu Wu, Xiang Liu, Weizhen Li, DongFang Li, Chen Zhao, WangXing Chen, LinLin Zheng, Zihui Li, GuangMing Guo, Jun Cell Death Dis Article The microtubule (MT) plus-end binding protein Clip170 is associated closely with breast cancer invasion and migration. In this study, Clip170 tension observed by a newly designed cpstFRET tension probe was suggested to be positive related to breast cancer aggressiveness, which could be regulated by α-tubulin detyrosination-induced MT disassembly. Clip170 phosphorylation induced by Ribosomal protein S6 kinase (RSK) could also increase its tension and promote the conversion of a discrete comet-like Clip-170 distribution into a spotty pattern during cancer metastasis. Heightened Clip170 tension was correlated with the formation of cortactin-associated filopodia and lamellipodia, and then promoted invasion and metastasis both in vitro and in vivo. Meanwhile, Clip170 tension enhanced at the leading edge in directional migration, accompanying with IQGAP1 subcellular distribution variation. Our work indicates that the malignancy and directionality during breast cancer migration depend on the magnitude and polarization of Clip170 tension, and we suggest Clip170 tension as a new potential drug target for breast cancer therapy. Nature Publishing Group UK 2022-10-08 /pmc/articles/PMC9547975/ /pubmed/36209218 http://dx.doi.org/10.1038/s41419-022-05306-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hu, Yunfeng Xie, Qiu Wu, Xiang Liu, Weizhen Li, DongFang Li, Chen Zhao, WangXing Chen, LinLin Zheng, Zihui Li, GuangMing Guo, Jun Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration |
title | Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration |
title_full | Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration |
title_fullStr | Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration |
title_full_unstemmed | Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration |
title_short | Tension of plus-end tracking protein Clip170 confers directionality and aggressiveness during breast cancer migration |
title_sort | tension of plus-end tracking protein clip170 confers directionality and aggressiveness during breast cancer migration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9547975/ https://www.ncbi.nlm.nih.gov/pubmed/36209218 http://dx.doi.org/10.1038/s41419-022-05306-6 |
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