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Ets-1 enhances tumor migration through regulation of CCR7 expression
Ets-1 is a prototype of the ETS protein family. Members of the ETS protein family contain a unique ETS domain. Ets-1 is associated with cancer progression and metastasis in many types of cancer. Many studies have shown a link between elevated expression of Ets-1 in cancer biopsies and poor survival....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774420/ https://www.ncbi.nlm.nih.gov/pubmed/31072446 http://dx.doi.org/10.5483/BMBRep.2019.52.9.232 |
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author | Fang, Li-Wen Kao, Ying-Hsien Chuang, Ya-Ting Huang, Huey-Lan Tai, Tzong-Shyuan |
author_facet | Fang, Li-Wen Kao, Ying-Hsien Chuang, Ya-Ting Huang, Huey-Lan Tai, Tzong-Shyuan |
author_sort | Fang, Li-Wen |
collection | PubMed |
description | Ets-1 is a prototype of the ETS protein family. Members of the ETS protein family contain a unique ETS domain. Ets-1 is associated with cancer progression and metastasis in many types of cancer. Many studies have shown a link between elevated expression of Ets-1 in cancer biopsies and poor survival. CCR7 is a chemokine that binds to specific ligand CCL21/CCL19. CCR7 expression is associated with tumor metastasis and infiltration into lymph nodes. The objective of this study was to test whether Ets-1 could regulate CCR7 expression and enhance tumor metastasis. Our data showed that CCR7 expression was downregulated in Ets-1-deficient T cells upon T-cell stimulation. Overexpression of Ets-1 increased CCR7 expression in breast cancer cell lines. In contrast, knockdown of Ets-1 reduced CCR7 expression. Ets-1 could directly bind to CCR7 promoter and mediate CCR7 expression in luciferase reporter assays and chromatin immunoprecipitation assays. Transactivation activity of Ets-1 was independent of the Pointed domain of Ets-1. Ets-1 could also enhance NF-κB and CBP transactivation of CCR7 promoter. Our results also showed that Ets-1 could modulate cancer cell transmigration by altering CCR7 expression in transwell assay and wound healing assay. Taken together, our data suggest that Ets-1 can enhance CCR7 expression and contribute to tumor cell migration. |
format | Online Article Text |
id | pubmed-6774420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-67744202019-10-09 Ets-1 enhances tumor migration through regulation of CCR7 expression Fang, Li-Wen Kao, Ying-Hsien Chuang, Ya-Ting Huang, Huey-Lan Tai, Tzong-Shyuan BMB Rep Articles Ets-1 is a prototype of the ETS protein family. Members of the ETS protein family contain a unique ETS domain. Ets-1 is associated with cancer progression and metastasis in many types of cancer. Many studies have shown a link between elevated expression of Ets-1 in cancer biopsies and poor survival. CCR7 is a chemokine that binds to specific ligand CCL21/CCL19. CCR7 expression is associated with tumor metastasis and infiltration into lymph nodes. The objective of this study was to test whether Ets-1 could regulate CCR7 expression and enhance tumor metastasis. Our data showed that CCR7 expression was downregulated in Ets-1-deficient T cells upon T-cell stimulation. Overexpression of Ets-1 increased CCR7 expression in breast cancer cell lines. In contrast, knockdown of Ets-1 reduced CCR7 expression. Ets-1 could directly bind to CCR7 promoter and mediate CCR7 expression in luciferase reporter assays and chromatin immunoprecipitation assays. Transactivation activity of Ets-1 was independent of the Pointed domain of Ets-1. Ets-1 could also enhance NF-κB and CBP transactivation of CCR7 promoter. Our results also showed that Ets-1 could modulate cancer cell transmigration by altering CCR7 expression in transwell assay and wound healing assay. Taken together, our data suggest that Ets-1 can enhance CCR7 expression and contribute to tumor cell migration. Korean Society for Biochemistry and Molecular Biology 2019-09 2019-09-30 /pmc/articles/PMC6774420/ /pubmed/31072446 http://dx.doi.org/10.5483/BMBRep.2019.52.9.232 Text en Copyright © 2019 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Fang, Li-Wen Kao, Ying-Hsien Chuang, Ya-Ting Huang, Huey-Lan Tai, Tzong-Shyuan Ets-1 enhances tumor migration through regulation of CCR7 expression |
title | Ets-1 enhances tumor migration through regulation of CCR7 expression |
title_full | Ets-1 enhances tumor migration through regulation of CCR7 expression |
title_fullStr | Ets-1 enhances tumor migration through regulation of CCR7 expression |
title_full_unstemmed | Ets-1 enhances tumor migration through regulation of CCR7 expression |
title_short | Ets-1 enhances tumor migration through regulation of CCR7 expression |
title_sort | ets-1 enhances tumor migration through regulation of ccr7 expression |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774420/ https://www.ncbi.nlm.nih.gov/pubmed/31072446 http://dx.doi.org/10.5483/BMBRep.2019.52.9.232 |
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