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Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression

Disintegrin-metalloproteinase 15(ADAM15), a member of disintegrin metalloproteinases (ADAMs), plays important roles in various cancer types. However, the underlying ADAM15 functioning in lung cancer is still unclear. In the present study, we find that ADAM15 regulates the epidermal growth factor rec...

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Autores principales: Zhou, Jieqi, Wang, Anqi, Cai, Tingting, Li, Yue, Du, Wenwen, Zhang, Yang, Zhang, Ruochen, Zhang, Weijie, Zhu, Jianjie, Zeng, Yuanyuan, Huang, Jian-an, Liu, Zeyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124216/
https://www.ncbi.nlm.nih.gov/pubmed/35597804
http://dx.doi.org/10.1038/s41419-022-04928-0
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author Zhou, Jieqi
Wang, Anqi
Cai, Tingting
Li, Yue
Du, Wenwen
Zhang, Yang
Zhang, Ruochen
Zhang, Weijie
Zhu, Jianjie
Zeng, Yuanyuan
Huang, Jian-an
Liu, Zeyi
author_facet Zhou, Jieqi
Wang, Anqi
Cai, Tingting
Li, Yue
Du, Wenwen
Zhang, Yang
Zhang, Ruochen
Zhang, Weijie
Zhu, Jianjie
Zeng, Yuanyuan
Huang, Jian-an
Liu, Zeyi
author_sort Zhou, Jieqi
collection PubMed
description Disintegrin-metalloproteinase 15(ADAM15), a member of disintegrin metalloproteinases (ADAMs), plays important roles in various cancer types. However, the underlying ADAM15 functioning in lung cancer is still unclear. In the present study, we find that ADAM15 regulates the epidermal growth factor receptor/focal adhesion kinase (EGFR/FAK) signalling pathway by interactions with integrins. Integrin αV is involved in ADAM15-mediated FAK signalling. Further, we find that ADAM15 and CD151 were co-expressed, and the presence of ADAM15 affected the integrin α3/α6-related EGFR signalling pathway by cooperating with CD151. In addition, we also prove the effect of ADAM15 on proliferation in nude mice. Finally, we show that ADAM15 is a direct target of miR-204-5p by luciferase reporter assays, qRT-PCR and western blot analyses. Our findings provide molecular and cellular evidence that ADAM15 promotes cell proliferation and metastasis in NSCLC, which might provide a potential target for NSCLC treatment.
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spelling pubmed-91242162022-05-23 Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression Zhou, Jieqi Wang, Anqi Cai, Tingting Li, Yue Du, Wenwen Zhang, Yang Zhang, Ruochen Zhang, Weijie Zhu, Jianjie Zeng, Yuanyuan Huang, Jian-an Liu, Zeyi Cell Death Dis Article Disintegrin-metalloproteinase 15(ADAM15), a member of disintegrin metalloproteinases (ADAMs), plays important roles in various cancer types. However, the underlying ADAM15 functioning in lung cancer is still unclear. In the present study, we find that ADAM15 regulates the epidermal growth factor receptor/focal adhesion kinase (EGFR/FAK) signalling pathway by interactions with integrins. Integrin αV is involved in ADAM15-mediated FAK signalling. Further, we find that ADAM15 and CD151 were co-expressed, and the presence of ADAM15 affected the integrin α3/α6-related EGFR signalling pathway by cooperating with CD151. In addition, we also prove the effect of ADAM15 on proliferation in nude mice. Finally, we show that ADAM15 is a direct target of miR-204-5p by luciferase reporter assays, qRT-PCR and western blot analyses. Our findings provide molecular and cellular evidence that ADAM15 promotes cell proliferation and metastasis in NSCLC, which might provide a potential target for NSCLC treatment. Nature Publishing Group UK 2022-05-21 /pmc/articles/PMC9124216/ /pubmed/35597804 http://dx.doi.org/10.1038/s41419-022-04928-0 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
Zhou, Jieqi
Wang, Anqi
Cai, Tingting
Li, Yue
Du, Wenwen
Zhang, Yang
Zhang, Ruochen
Zhang, Weijie
Zhu, Jianjie
Zeng, Yuanyuan
Huang, Jian-an
Liu, Zeyi
Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression
title Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression
title_full Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression
title_fullStr Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression
title_full_unstemmed Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression
title_short Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression
title_sort integrin α3/α6 and αv are implicated in adam15-activated fak and egfr signalling pathway individually and promote non-small-cell lung cancer progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124216/
https://www.ncbi.nlm.nih.gov/pubmed/35597804
http://dx.doi.org/10.1038/s41419-022-04928-0
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