Cargando…

MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis

Gastric cancer (GC) is a major cause of human deaths worldwide, and is notorious for its high incidence and mortality rates. Mesoderm Posterior Basic Helix-loop-helix (bHLH) transcription factor 2 (MESP2) acts as a transcription factor with a conserved bHLH domain. However, whether MESP2 contributes...

Descripción completa

Detalles Bibliográficos
Autores principales: Ge, Lingjun, Zhao, Gaichao, Lan, Chao, Song, Houji, Qi, Dan, Huang, Pan, Ke, Xiaoxue, Cui, Hongjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975210/
https://www.ncbi.nlm.nih.gov/pubmed/36854722
http://dx.doi.org/10.1038/s41420-023-01367-4
_version_ 1784898825224192000
author Ge, Lingjun
Zhao, Gaichao
Lan, Chao
Song, Houji
Qi, Dan
Huang, Pan
Ke, Xiaoxue
Cui, Hongjuan
author_facet Ge, Lingjun
Zhao, Gaichao
Lan, Chao
Song, Houji
Qi, Dan
Huang, Pan
Ke, Xiaoxue
Cui, Hongjuan
author_sort Ge, Lingjun
collection PubMed
description Gastric cancer (GC) is a major cause of human deaths worldwide, and is notorious for its high incidence and mortality rates. Mesoderm Posterior Basic Helix-loop-helix (bHLH) transcription factor 2 (MESP2) acts as a transcription factor with a conserved bHLH domain. However, whether MESP2 contributes to tumorigenesis and its potential molecular mechanisms, remain unexplored. Noticeably, MESP2 expression levels are decreased in GC tissues and cell lines compared to those in normal tissue. Further, in vitro and in vivo experiments have confirmed that MESP2 overexpression suppresses GC cell growth, migration, and invasion, whereas MESP2 knockdown results in the exact opposite. Here, we present the first report that MESP2 binds to transcription factor 7-like 2 (TCF7L2/TCF4) to inhibit the activation of the TCF4/beta-catenin transcriptional complex, decrease the occupancy of the complex on the S-phase kinase Associated Protein 2 (SKP2) promoter, and promote p27 accumulation. MESP2 knockdown facilitated tumorigenesis, which was partially suppressed by SKP2 knockdown. Taken together, we conclude that MESP2 binds competitively to TCF4 to suppress GC progression by regulating the SKP2/p27 axis, thus offering a potential therapeutic strategy for future treatment.
format Online
Article
Text
id pubmed-9975210
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-99752102023-03-02 MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis Ge, Lingjun Zhao, Gaichao Lan, Chao Song, Houji Qi, Dan Huang, Pan Ke, Xiaoxue Cui, Hongjuan Cell Death Discov Article Gastric cancer (GC) is a major cause of human deaths worldwide, and is notorious for its high incidence and mortality rates. Mesoderm Posterior Basic Helix-loop-helix (bHLH) transcription factor 2 (MESP2) acts as a transcription factor with a conserved bHLH domain. However, whether MESP2 contributes to tumorigenesis and its potential molecular mechanisms, remain unexplored. Noticeably, MESP2 expression levels are decreased in GC tissues and cell lines compared to those in normal tissue. Further, in vitro and in vivo experiments have confirmed that MESP2 overexpression suppresses GC cell growth, migration, and invasion, whereas MESP2 knockdown results in the exact opposite. Here, we present the first report that MESP2 binds to transcription factor 7-like 2 (TCF7L2/TCF4) to inhibit the activation of the TCF4/beta-catenin transcriptional complex, decrease the occupancy of the complex on the S-phase kinase Associated Protein 2 (SKP2) promoter, and promote p27 accumulation. MESP2 knockdown facilitated tumorigenesis, which was partially suppressed by SKP2 knockdown. Taken together, we conclude that MESP2 binds competitively to TCF4 to suppress GC progression by regulating the SKP2/p27 axis, thus offering a potential therapeutic strategy for future treatment. Nature Publishing Group UK 2023-03-01 /pmc/articles/PMC9975210/ /pubmed/36854722 http://dx.doi.org/10.1038/s41420-023-01367-4 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 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
Ge, Lingjun
Zhao, Gaichao
Lan, Chao
Song, Houji
Qi, Dan
Huang, Pan
Ke, Xiaoxue
Cui, Hongjuan
MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis
title MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis
title_full MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis
title_fullStr MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis
title_full_unstemmed MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis
title_short MESP2 binds competitively to TCF4 to suppress gastric cancer progression by regulating the SKP2/p27 axis
title_sort mesp2 binds competitively to tcf4 to suppress gastric cancer progression by regulating the skp2/p27 axis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975210/
https://www.ncbi.nlm.nih.gov/pubmed/36854722
http://dx.doi.org/10.1038/s41420-023-01367-4
work_keys_str_mv AT gelingjun mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis
AT zhaogaichao mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis
AT lanchao mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis
AT songhouji mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis
AT qidan mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis
AT huangpan mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis
AT kexiaoxue mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis
AT cuihongjuan mesp2bindscompetitivelytotcf4tosuppressgastriccancerprogressionbyregulatingtheskp2p27axis