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Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins
BACKGROUND: Formin-like 2 (FMNL2) is a member of Formin family which governs cytokinesis, cellular polarity and morphogenesis. Dysregulation of FMNL2 has been discovered in cancers and is closely related to cancers. However, the role of FMNL2 in gastric cancer remains unclear. In this study, we aime...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984784/ https://www.ncbi.nlm.nih.gov/pubmed/29881327 http://dx.doi.org/10.1186/s12935-018-0576-1 |
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author | Zhong, Banghua Wang, Kewei Xu, Hao Kong, Fanmin |
author_facet | Zhong, Banghua Wang, Kewei Xu, Hao Kong, Fanmin |
author_sort | Zhong, Banghua |
collection | PubMed |
description | BACKGROUND: Formin-like 2 (FMNL2) is a member of Formin family which governs cytokinesis, cellular polarity and morphogenesis. Dysregulation of FMNL2 has been discovered in cancers and is closely related to cancers. However, the role of FMNL2 in gastric cancer remains unclear. In this study, we aimed to investigate the role of FMNL2 in gastric cancer cells. METHODS: A FMNL2-specific shRNA was employed to decrease the endogenous expression of FMNL2. Then the degree of proliferation, apoptosis, migration and invasion of gastric cancer cells was assessed by MTT assay, flow cytometry, wound healing assay and transwell assay, respectively. The expression and distribution of FMNL2 and protein kinase C (PKC) α was detected by immunofluorescence. The internalization of integrins was detected by enzyme-linked immunosorbent assay. RESULTS: Our results showed that silencing FMNL2 suppressed proliferation, migration and invasion, and induced apoptosis of gastric cancer cells. The integrin internalization induced by PKC was declined by FMNL2 silencing. CONCLUSIONS: Our study reveals that silencing FMNL2 suppresses growth and metastasis of gastric cancer cells. Modulation on integrin internalization may be implicated in the role of FMNL2 in growth and migration of gastric cancer cells. Our study indicates that FMNL2 may become a potential therapeutic target for gastric cancer. |
format | Online Article Text |
id | pubmed-5984784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59847842018-06-07 Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins Zhong, Banghua Wang, Kewei Xu, Hao Kong, Fanmin Cancer Cell Int Primary Research BACKGROUND: Formin-like 2 (FMNL2) is a member of Formin family which governs cytokinesis, cellular polarity and morphogenesis. Dysregulation of FMNL2 has been discovered in cancers and is closely related to cancers. However, the role of FMNL2 in gastric cancer remains unclear. In this study, we aimed to investigate the role of FMNL2 in gastric cancer cells. METHODS: A FMNL2-specific shRNA was employed to decrease the endogenous expression of FMNL2. Then the degree of proliferation, apoptosis, migration and invasion of gastric cancer cells was assessed by MTT assay, flow cytometry, wound healing assay and transwell assay, respectively. The expression and distribution of FMNL2 and protein kinase C (PKC) α was detected by immunofluorescence. The internalization of integrins was detected by enzyme-linked immunosorbent assay. RESULTS: Our results showed that silencing FMNL2 suppressed proliferation, migration and invasion, and induced apoptosis of gastric cancer cells. The integrin internalization induced by PKC was declined by FMNL2 silencing. CONCLUSIONS: Our study reveals that silencing FMNL2 suppresses growth and metastasis of gastric cancer cells. Modulation on integrin internalization may be implicated in the role of FMNL2 in growth and migration of gastric cancer cells. Our study indicates that FMNL2 may become a potential therapeutic target for gastric cancer. BioMed Central 2018-06-01 /pmc/articles/PMC5984784/ /pubmed/29881327 http://dx.doi.org/10.1186/s12935-018-0576-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Primary Research Zhong, Banghua Wang, Kewei Xu, Hao Kong, Fanmin Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins |
title | Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins |
title_full | Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins |
title_fullStr | Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins |
title_full_unstemmed | Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins |
title_short | Silencing Formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins |
title_sort | silencing formin-like 2 inhibits growth and metastasis of gastric cancer cells through suppressing internalization of integrins |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984784/ https://www.ncbi.nlm.nih.gov/pubmed/29881327 http://dx.doi.org/10.1186/s12935-018-0576-1 |
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