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BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin

BECN1/Beclin1 is one of the key proteins in autophagy regulation. However, the biological functions of BECN1 in non-small cell lung cancer (NSCLC) were obscure. Here, we found that neither BECN1 knockdown nor overexpression affected the proliferation of NSCLC cells. Surprisingly, BECN1 overexpressio...

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Autores principales: Cheng, Zhujun, Xin, Hongbo, Han, Tianyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629178/
https://www.ncbi.nlm.nih.gov/pubmed/31272261
http://dx.doi.org/10.1080/19336918.2019.1638690
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author Cheng, Zhujun
Xin, Hongbo
Han, Tianyu
author_facet Cheng, Zhujun
Xin, Hongbo
Han, Tianyu
author_sort Cheng, Zhujun
collection PubMed
description BECN1/Beclin1 is one of the key proteins in autophagy regulation. However, the biological functions of BECN1 in non-small cell lung cancer (NSCLC) were obscure. Here, we found that neither BECN1 knockdown nor overexpression affected the proliferation of NSCLC cells. Surprisingly, BECN1 overexpression increased cell migration and knocking down BECN1 significantly reduced the migratory ability of NSCLC cells. We further demonstrated that BECN1 could interact with Vimentin and affected its K48-linked ubiquitination. What’s more, BECN1 could also interact with ubiquitin-specific peptidase 14 (USP14), the key de-ubiquitinase of Vimentin, and regulated USP14 mediated de-ubiquitination of Vimentin. Thus, our studies revealed an oncosupportive role of BECN1 in the migration of NSCLC cells through regulating the ubiquitination of Vimentin.
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spelling pubmed-66291782019-07-18 BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin Cheng, Zhujun Xin, Hongbo Han, Tianyu Cell Adh Migr Research Paper BECN1/Beclin1 is one of the key proteins in autophagy regulation. However, the biological functions of BECN1 in non-small cell lung cancer (NSCLC) were obscure. Here, we found that neither BECN1 knockdown nor overexpression affected the proliferation of NSCLC cells. Surprisingly, BECN1 overexpression increased cell migration and knocking down BECN1 significantly reduced the migratory ability of NSCLC cells. We further demonstrated that BECN1 could interact with Vimentin and affected its K48-linked ubiquitination. What’s more, BECN1 could also interact with ubiquitin-specific peptidase 14 (USP14), the key de-ubiquitinase of Vimentin, and regulated USP14 mediated de-ubiquitination of Vimentin. Thus, our studies revealed an oncosupportive role of BECN1 in the migration of NSCLC cells through regulating the ubiquitination of Vimentin. Taylor & Francis 2019-07-05 /pmc/articles/PMC6629178/ /pubmed/31272261 http://dx.doi.org/10.1080/19336918.2019.1638690 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Cheng, Zhujun
Xin, Hongbo
Han, Tianyu
BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin
title BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin
title_full BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin
title_fullStr BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin
title_full_unstemmed BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin
title_short BECN1 promotes the migration of NSCLC cells through regulating the ubiquitination of Vimentin
title_sort becn1 promotes the migration of nsclc cells through regulating the ubiquitination of vimentin
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629178/
https://www.ncbi.nlm.nih.gov/pubmed/31272261
http://dx.doi.org/10.1080/19336918.2019.1638690
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