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Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis

Networks of nanotubes and microtubules are highly valued in cellular communication, and collective cancer movement has been revealed to be associated with cell information exchange. In the present study, cellular communication was demonstrated to participate in mammosphere growth, differentiation an...

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Autores principales: Huang, Shangke, Yuan, Na, Wang, Guanying, Wu, Fang, Feng, Lu, Luo, Minna, Li, Miao, Luo, Anqi, Zhao, Xinhan, Zhang, Lingxiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196647/
https://www.ncbi.nlm.nih.gov/pubmed/30542711
http://dx.doi.org/10.3892/or.2018.6778
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author Huang, Shangke
Yuan, Na
Wang, Guanying
Wu, Fang
Feng, Lu
Luo, Minna
Li, Miao
Luo, Anqi
Zhao, Xinhan
Zhang, Lingxiao
author_facet Huang, Shangke
Yuan, Na
Wang, Guanying
Wu, Fang
Feng, Lu
Luo, Minna
Li, Miao
Luo, Anqi
Zhao, Xinhan
Zhang, Lingxiao
author_sort Huang, Shangke
collection PubMed
description Networks of nanotubes and microtubules are highly valued in cellular communication, and collective cancer movement has been revealed to be associated with cell information exchange. In the present study, cellular communication was demonstrated to participate in mammosphere growth, differentiation and collective invasion. By promoting differentiation, networks of cells and microtubule-like structures were verified. Analyses of cell cycle progression, stemness markers and gene expression indicated that mammospheres had collective characteristics of stemness and differentiation. Invasion assays revealed that networks of microtubule-like structures promoted collective invasion. Conversely, using anti-angiogenic intervention, the growth of stem-like mammospheres and cellular communication links were effectively inhibited. In vivo experiments revealed that cellular communication promoted tumor growth and metastasis through the formation of nodular fusion, cluttered microtubule-like structures and cancer stem cells, as well as vascular niches. In conclusion, the present results demonstrated that a network of cells and structures were largely present in mammosphere cellular communication in vitro and in vivo. Therefore, blocking cellular communication may prove beneficial in halting the progression of mammary tumors.
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spelling pubmed-61966472018-10-23 Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis Huang, Shangke Yuan, Na Wang, Guanying Wu, Fang Feng, Lu Luo, Minna Li, Miao Luo, Anqi Zhao, Xinhan Zhang, Lingxiao Oncol Rep Articles Networks of nanotubes and microtubules are highly valued in cellular communication, and collective cancer movement has been revealed to be associated with cell information exchange. In the present study, cellular communication was demonstrated to participate in mammosphere growth, differentiation and collective invasion. By promoting differentiation, networks of cells and microtubule-like structures were verified. Analyses of cell cycle progression, stemness markers and gene expression indicated that mammospheres had collective characteristics of stemness and differentiation. Invasion assays revealed that networks of microtubule-like structures promoted collective invasion. Conversely, using anti-angiogenic intervention, the growth of stem-like mammospheres and cellular communication links were effectively inhibited. In vivo experiments revealed that cellular communication promoted tumor growth and metastasis through the formation of nodular fusion, cluttered microtubule-like structures and cancer stem cells, as well as vascular niches. In conclusion, the present results demonstrated that a network of cells and structures were largely present in mammosphere cellular communication in vitro and in vivo. Therefore, blocking cellular communication may prove beneficial in halting the progression of mammary tumors. D.A. Spandidos 2018-12 2018-10-09 /pmc/articles/PMC6196647/ /pubmed/30542711 http://dx.doi.org/10.3892/or.2018.6778 Text en Copyright: © Huang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Huang, Shangke
Yuan, Na
Wang, Guanying
Wu, Fang
Feng, Lu
Luo, Minna
Li, Miao
Luo, Anqi
Zhao, Xinhan
Zhang, Lingxiao
Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis
title Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis
title_full Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis
title_fullStr Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis
title_full_unstemmed Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis
title_short Cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis
title_sort cellular communication promotes mammosphere growth and collective invasion through microtubule-like structures and angiogenesis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196647/
https://www.ncbi.nlm.nih.gov/pubmed/30542711
http://dx.doi.org/10.3892/or.2018.6778
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