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MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor
BACKGROUND: The Mitogen-activated protein kinase 1 (MAPK1) has both independent functions of phosphorylating histones as a kinase and directly binding the promoter regions of genes to regulate gene expression as a transcription factor. Previous studies have identified elevated expression of MAPK1 in...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563293/ https://www.ncbi.nlm.nih.gov/pubmed/37817112 http://dx.doi.org/10.1186/s12885-023-11480-3 |
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author | Wang, Yue Guo, Zheng Tian, Yueli Cong, Liang Zheng, Yulu Wu, Zhiyuan Shan, Guangle Xia, Yao Zhu, Yahong Li, Xingang Song, Ying |
author_facet | Wang, Yue Guo, Zheng Tian, Yueli Cong, Liang Zheng, Yulu Wu, Zhiyuan Shan, Guangle Xia, Yao Zhu, Yahong Li, Xingang Song, Ying |
author_sort | Wang, Yue |
collection | PubMed |
description | BACKGROUND: The Mitogen-activated protein kinase 1 (MAPK1) has both independent functions of phosphorylating histones as a kinase and directly binding the promoter regions of genes to regulate gene expression as a transcription factor. Previous studies have identified elevated expression of MAPK1 in human gastric cancer, which is associated with its role as a kinase, facilitating the migration and invasion of gastric cancer cells. However, how MAPK1 binds to its target genes as a transcription factor and whether it modulates related gene expressions in gastric cancer remains unclear. RESULTS: Here, we integrated biochemical assays (protein interactions and chromatin immunoprecipitation (ChIP)), cellular analysis assays (cell proliferation and migration), RNA sequencing, ChIP sequencing, and clinical analysis to investigate the potential genomic recognition patterns of MAPK1 in a human gastric adenocarcinoma cell-line (AGS) and to uncover its regulatory effect on gastric cancer progression. We confirmed that MAPK1 promotes AGS cells invasion and migration by regulating the target genes in different directions, up-regulating seven target genes (KRT13, KRT6A, KRT81, MYH15, STARD4, SYTL4, and TMEM267) and down-regulating one gene (FGG). Among them, five genes (FGG, MYH15, STARD4, SYTL4, and TMEM267) were first associated with cancer procession, while the other three (KRT81, KRT6A, and KRT13) have previously been confirmed to be related to cancer metastasis and migration. CONCLUSION: Our data showed that MAPK1 can bind to the promoter regions of these target genes to control their transcription as a bidirectional transcription factor, promoting AGS cell motility and invasion. Our research has expanded the understanding of the regulatory roles of MAPK1, enriched our knowledge of transcription factors, and provided novel candidates for cancer therapeutics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11480-3. |
format | Online Article Text |
id | pubmed-10563293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105632932023-10-11 MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor Wang, Yue Guo, Zheng Tian, Yueli Cong, Liang Zheng, Yulu Wu, Zhiyuan Shan, Guangle Xia, Yao Zhu, Yahong Li, Xingang Song, Ying BMC Cancer Research BACKGROUND: The Mitogen-activated protein kinase 1 (MAPK1) has both independent functions of phosphorylating histones as a kinase and directly binding the promoter regions of genes to regulate gene expression as a transcription factor. Previous studies have identified elevated expression of MAPK1 in human gastric cancer, which is associated with its role as a kinase, facilitating the migration and invasion of gastric cancer cells. However, how MAPK1 binds to its target genes as a transcription factor and whether it modulates related gene expressions in gastric cancer remains unclear. RESULTS: Here, we integrated biochemical assays (protein interactions and chromatin immunoprecipitation (ChIP)), cellular analysis assays (cell proliferation and migration), RNA sequencing, ChIP sequencing, and clinical analysis to investigate the potential genomic recognition patterns of MAPK1 in a human gastric adenocarcinoma cell-line (AGS) and to uncover its regulatory effect on gastric cancer progression. We confirmed that MAPK1 promotes AGS cells invasion and migration by regulating the target genes in different directions, up-regulating seven target genes (KRT13, KRT6A, KRT81, MYH15, STARD4, SYTL4, and TMEM267) and down-regulating one gene (FGG). Among them, five genes (FGG, MYH15, STARD4, SYTL4, and TMEM267) were first associated with cancer procession, while the other three (KRT81, KRT6A, and KRT13) have previously been confirmed to be related to cancer metastasis and migration. CONCLUSION: Our data showed that MAPK1 can bind to the promoter regions of these target genes to control their transcription as a bidirectional transcription factor, promoting AGS cell motility and invasion. Our research has expanded the understanding of the regulatory roles of MAPK1, enriched our knowledge of transcription factors, and provided novel candidates for cancer therapeutics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11480-3. BioMed Central 2023-10-10 /pmc/articles/PMC10563293/ /pubmed/37817112 http://dx.doi.org/10.1186/s12885-023-11480-3 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wang, Yue Guo, Zheng Tian, Yueli Cong, Liang Zheng, Yulu Wu, Zhiyuan Shan, Guangle Xia, Yao Zhu, Yahong Li, Xingang Song, Ying MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor |
title | MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor |
title_full | MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor |
title_fullStr | MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor |
title_full_unstemmed | MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor |
title_short | MAPK1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor |
title_sort | mapk1 promotes the metastasis and invasion of gastric cancer as a bidirectional transcription factor |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563293/ https://www.ncbi.nlm.nih.gov/pubmed/37817112 http://dx.doi.org/10.1186/s12885-023-11480-3 |
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