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Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion

Claudin-4, a member of the claudin multigene family, participates in events associated with mesenchymal-like activity of cancerous cells. Claudin-4 expression is upregulated in cervical cancer tissue compared with that in adjoining non-neoplastic tissue. However, the mechanisms that regulate Claudin...

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Autores principales: Zhu, Jiaqi, Jiang, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326656/
https://www.ncbi.nlm.nih.gov/pubmed/37427351
http://dx.doi.org/10.3892/ol.2023.13921
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author Zhu, Jiaqi
Jiang, Qi
author_facet Zhu, Jiaqi
Jiang, Qi
author_sort Zhu, Jiaqi
collection PubMed
description Claudin-4, a member of the claudin multigene family, participates in events associated with mesenchymal-like activity of cancerous cells. Claudin-4 expression is upregulated in cervical cancer tissue compared with that in adjoining non-neoplastic tissue. However, the mechanisms that regulate Claudin-4 expression in cervical cancer are poorly understood. Moreover, whether Claudin-4 contributes to the migration and invasion of cervical cancer cells remains unclear. By western blotting, reverse transcription-qPCR, bioinformatics analysis, dual-luciferase reporter assay, chromatin immunoprecipitation assay, wound healing assay and Transwell migration/invasion assay, the present study confirmed that Claudin-4 was a downstream target of Twist1, a helix-loop-helix transcriptional factor, the activity of which has a positive correlation with Claudin-4 expression. Mechanistically, Twist1 directly binds to Claudin-4 promoter, resulting in the transactivation of expression. The depletion of the Twist1-binding E-Box1 domain on Claudin-4 promoter via CRISPR-Cas9 knockout system downregulates Claudin-4 expression and suppresses the ability of cervical cancer cells to migrate and invade by elevating E-cadherin levels and lowering N-cadherin levels. Following activation by transforming growth factor-β, Twist1 induces Claudin-4 expression, thus enhancing migration and invasion of cervical cancer cells. In summary, the present data suggested that Claudin-4 was a direct downstream target of Twist1 and served a critical role in promoting Twist1-mediated cervical cancer cell migration and invasion.
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spelling pubmed-103266562023-07-08 Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion Zhu, Jiaqi Jiang, Qi Oncol Lett Articles Claudin-4, a member of the claudin multigene family, participates in events associated with mesenchymal-like activity of cancerous cells. Claudin-4 expression is upregulated in cervical cancer tissue compared with that in adjoining non-neoplastic tissue. However, the mechanisms that regulate Claudin-4 expression in cervical cancer are poorly understood. Moreover, whether Claudin-4 contributes to the migration and invasion of cervical cancer cells remains unclear. By western blotting, reverse transcription-qPCR, bioinformatics analysis, dual-luciferase reporter assay, chromatin immunoprecipitation assay, wound healing assay and Transwell migration/invasion assay, the present study confirmed that Claudin-4 was a downstream target of Twist1, a helix-loop-helix transcriptional factor, the activity of which has a positive correlation with Claudin-4 expression. Mechanistically, Twist1 directly binds to Claudin-4 promoter, resulting in the transactivation of expression. The depletion of the Twist1-binding E-Box1 domain on Claudin-4 promoter via CRISPR-Cas9 knockout system downregulates Claudin-4 expression and suppresses the ability of cervical cancer cells to migrate and invade by elevating E-cadherin levels and lowering N-cadherin levels. Following activation by transforming growth factor-β, Twist1 induces Claudin-4 expression, thus enhancing migration and invasion of cervical cancer cells. In summary, the present data suggested that Claudin-4 was a direct downstream target of Twist1 and served a critical role in promoting Twist1-mediated cervical cancer cell migration and invasion. D.A. Spandidos 2023-06-20 /pmc/articles/PMC10326656/ /pubmed/37427351 http://dx.doi.org/10.3892/ol.2023.13921 Text en Copyright: © Zhu et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhu, Jiaqi
Jiang, Qi
Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion
title Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion
title_full Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion
title_fullStr Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion
title_full_unstemmed Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion
title_short Twist1‑mediated transcriptional activation of Claudin‑4 promotes cervical cancer cell migration and invasion
title_sort twist1‑mediated transcriptional activation of claudin‑4 promotes cervical cancer cell migration and invasion
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326656/
https://www.ncbi.nlm.nih.gov/pubmed/37427351
http://dx.doi.org/10.3892/ol.2023.13921
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