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Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma

Transcription factor 3 (TCF3) is a member of the basic Helix – Loop – Helix (bHLH) transcription factor (TF) family and is encoded by the TCF3 gene (also known as E2A). It has been shown that TCF3 functions as a key transcription factor in the pathogenesis of several human cancers and plays an impor...

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Autores principales: Li, Zhao-Xing, Sun, Ming-Chuang, Fang, Kang, Zhao, Zi-Ying, Leng, Zhu-Yun, Zhang, Ze-Hua, Xu, Ai-Ping, Chu, Yuan, Zhang, Li, Lian, Jingjing, Chen, Tao, Xu, Mei-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443991/
https://www.ncbi.nlm.nih.gov/pubmed/37607071
http://dx.doi.org/10.1080/15384047.2023.2246206
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author Li, Zhao-Xing
Sun, Ming-Chuang
Fang, Kang
Zhao, Zi-Ying
Leng, Zhu-Yun
Zhang, Ze-Hua
Xu, Ai-Ping
Chu, Yuan
Zhang, Li
Lian, Jingjing
Chen, Tao
Xu, Mei-Dong
author_facet Li, Zhao-Xing
Sun, Ming-Chuang
Fang, Kang
Zhao, Zi-Ying
Leng, Zhu-Yun
Zhang, Ze-Hua
Xu, Ai-Ping
Chu, Yuan
Zhang, Li
Lian, Jingjing
Chen, Tao
Xu, Mei-Dong
author_sort Li, Zhao-Xing
collection PubMed
description Transcription factor 3 (TCF3) is a member of the basic Helix – Loop – Helix (bHLH) transcription factor (TF) family and is encoded by the TCF3 gene (also known as E2A). It has been shown that TCF3 functions as a key transcription factor in the pathogenesis of several human cancers and plays an important role in stem cell maintenance and carcinogenesis. However, the effect of TCF3 in the progression of esophageal squamous cell carcinoma (ESCC) is poorly known. In our study, TCF3 was found to express highly and correlated with cancer stage and prognosis. TCF3 was shown to promote ESCC invasion, migration, and drug resistance both from the results of in vivo and in vitro assays. Moreover, further studies suggested that TCF3 played these roles through transcriptionally regulating Inhibitor of DNA binding 1(ID1). Notably, we also found that TCF3 or ID1 was associated with ESCC stemness. Furthermore, TCF3 was correlated with the expression of cancer stemness markers CD44 and CD133. Therefore, maintaining cancer stemness might be the underlying mechanism that TCF3 transcriptionally regulated ID1 and further promoted ESCC progression and drug resistance.
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spelling pubmed-104439912023-08-23 Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma Li, Zhao-Xing Sun, Ming-Chuang Fang, Kang Zhao, Zi-Ying Leng, Zhu-Yun Zhang, Ze-Hua Xu, Ai-Ping Chu, Yuan Zhang, Li Lian, Jingjing Chen, Tao Xu, Mei-Dong Cancer Biol Ther Research Paper Transcription factor 3 (TCF3) is a member of the basic Helix – Loop – Helix (bHLH) transcription factor (TF) family and is encoded by the TCF3 gene (also known as E2A). It has been shown that TCF3 functions as a key transcription factor in the pathogenesis of several human cancers and plays an important role in stem cell maintenance and carcinogenesis. However, the effect of TCF3 in the progression of esophageal squamous cell carcinoma (ESCC) is poorly known. In our study, TCF3 was found to express highly and correlated with cancer stage and prognosis. TCF3 was shown to promote ESCC invasion, migration, and drug resistance both from the results of in vivo and in vitro assays. Moreover, further studies suggested that TCF3 played these roles through transcriptionally regulating Inhibitor of DNA binding 1(ID1). Notably, we also found that TCF3 or ID1 was associated with ESCC stemness. Furthermore, TCF3 was correlated with the expression of cancer stemness markers CD44 and CD133. Therefore, maintaining cancer stemness might be the underlying mechanism that TCF3 transcriptionally regulated ID1 and further promoted ESCC progression and drug resistance. Taylor & Francis 2023-08-21 /pmc/articles/PMC10443991/ /pubmed/37607071 http://dx.doi.org/10.1080/15384047.2023.2246206 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Paper
Li, Zhao-Xing
Sun, Ming-Chuang
Fang, Kang
Zhao, Zi-Ying
Leng, Zhu-Yun
Zhang, Ze-Hua
Xu, Ai-Ping
Chu, Yuan
Zhang, Li
Lian, Jingjing
Chen, Tao
Xu, Mei-Dong
Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma
title Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma
title_full Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma
title_fullStr Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma
title_full_unstemmed Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma
title_short Transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating ID1 expression in esophageal squamous cell carcinoma
title_sort transcription factor 3 promotes migration and invasion potential and maintains cancer stemness by activating id1 expression in esophageal squamous cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443991/
https://www.ncbi.nlm.nih.gov/pubmed/37607071
http://dx.doi.org/10.1080/15384047.2023.2246206
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