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BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK

BKCa is a large conductance calcium activated potassium channel promoting prostate cancer cell proliferation, although the mechanism is not fully elucidated. In addition, whether BKCa is involved in metastasis of prostate cancer remains to be explored. Here, we report that BKCa is overexpressed in p...

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Autores principales: Du, Cheng, Zheng, Zhendong, Li, Danqi, Chen, Li, Li, Na, Yi, Xiaomin, Yang, Yang, Guo, Fang, Liu, Wenchao, Xie, Xiaodong, Xie, Manjiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5130001/
https://www.ncbi.nlm.nih.gov/pubmed/27233075
http://dx.doi.org/10.18632/oncotarget.9559
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author Du, Cheng
Zheng, Zhendong
Li, Danqi
Chen, Li
Li, Na
Yi, Xiaomin
Yang, Yang
Guo, Fang
Liu, Wenchao
Xie, Xiaodong
Xie, Manjiang
author_facet Du, Cheng
Zheng, Zhendong
Li, Danqi
Chen, Li
Li, Na
Yi, Xiaomin
Yang, Yang
Guo, Fang
Liu, Wenchao
Xie, Xiaodong
Xie, Manjiang
author_sort Du, Cheng
collection PubMed
description BKCa is a large conductance calcium activated potassium channel promoting prostate cancer cell proliferation, although the mechanism is not fully elucidated. In addition, whether BKCa is involved in metastasis of prostate cancer remains to be explored. Here, we report that BKCa is overexpressed in prostate cancer. BKCa expression positively correlates with Ki67 index and gleason score of prostate cancer. Upregulation of BKCa promoted proliferation, migration and invasion of prostate cancer cells. On the contrary, downregulation of BKCa inhibited growth and metastasis of prostate cancer cells both in vitro and in vivo. Moreover, the ion-conducting function of BKCa contributed moderately to prostate cancer proliferation and migration, although, this was not the primary mechanism. BKCa action was mainly mediated through forming a functional complex with αvβ3 integrin. The BKCa/αvβ3 integrin complex promoted FAK phosphorylation independent of the channel activity. Overexpression of BKCa enhanced its association with αvβ3 integrin and FAK which increased FAK phosphorylation. Conversely, disrupting the complex by downregulation of BKCa reduced FAK phosphorylation. Finally, blocking of αvβ3 integrin or p-FAK activity using LM609 or Y15 markedly abrogated BKCa-enhanced cell proliferation and migration. Taken together, these results suggest that targeting BKCa/αvβ3/FAK may inaugurate innovative approaches to inhibit prostate cancer growth and metastasis.
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spelling pubmed-51300012016-12-11 BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK Du, Cheng Zheng, Zhendong Li, Danqi Chen, Li Li, Na Yi, Xiaomin Yang, Yang Guo, Fang Liu, Wenchao Xie, Xiaodong Xie, Manjiang Oncotarget Research Paper BKCa is a large conductance calcium activated potassium channel promoting prostate cancer cell proliferation, although the mechanism is not fully elucidated. In addition, whether BKCa is involved in metastasis of prostate cancer remains to be explored. Here, we report that BKCa is overexpressed in prostate cancer. BKCa expression positively correlates with Ki67 index and gleason score of prostate cancer. Upregulation of BKCa promoted proliferation, migration and invasion of prostate cancer cells. On the contrary, downregulation of BKCa inhibited growth and metastasis of prostate cancer cells both in vitro and in vivo. Moreover, the ion-conducting function of BKCa contributed moderately to prostate cancer proliferation and migration, although, this was not the primary mechanism. BKCa action was mainly mediated through forming a functional complex with αvβ3 integrin. The BKCa/αvβ3 integrin complex promoted FAK phosphorylation independent of the channel activity. Overexpression of BKCa enhanced its association with αvβ3 integrin and FAK which increased FAK phosphorylation. Conversely, disrupting the complex by downregulation of BKCa reduced FAK phosphorylation. Finally, blocking of αvβ3 integrin or p-FAK activity using LM609 or Y15 markedly abrogated BKCa-enhanced cell proliferation and migration. Taken together, these results suggest that targeting BKCa/αvβ3/FAK may inaugurate innovative approaches to inhibit prostate cancer growth and metastasis. Impact Journals LLC 2016-05-23 /pmc/articles/PMC5130001/ /pubmed/27233075 http://dx.doi.org/10.18632/oncotarget.9559 Text en Copyright: © 2016 Du 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
Du, Cheng
Zheng, Zhendong
Li, Danqi
Chen, Li
Li, Na
Yi, Xiaomin
Yang, Yang
Guo, Fang
Liu, Wenchao
Xie, Xiaodong
Xie, Manjiang
BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK
title BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK
title_full BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK
title_fullStr BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK
title_full_unstemmed BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK
title_short BKCa promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and FAK
title_sort bkca promotes growth and metastasis of prostate cancer through facilitating the coupling between αvβ3 integrin and fak
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5130001/
https://www.ncbi.nlm.nih.gov/pubmed/27233075
http://dx.doi.org/10.18632/oncotarget.9559
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