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TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling
Colorectal cancer (CRC) has become a major public health problem, ranking as the third most common type of cancer. Our previous study has revealed that TCF21 is frequently silenced by promoter hypermethylation in both CRC cell lines and primary CRC, with TCF21 methylation being significantly correla...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359128/ https://www.ncbi.nlm.nih.gov/pubmed/28352192 http://dx.doi.org/10.2147/OTT.S118151 |
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author | Dai, Youyi Duan, Huaxin Duan, Chaojun Zhu, Hong Zhou, Rongrong Pei, Haiping Shen, Liangfang |
author_facet | Dai, Youyi Duan, Huaxin Duan, Chaojun Zhu, Hong Zhou, Rongrong Pei, Haiping Shen, Liangfang |
author_sort | Dai, Youyi |
collection | PubMed |
description | Colorectal cancer (CRC) has become a major public health problem, ranking as the third most common type of cancer. Our previous study has revealed that TCF21 is frequently silenced by promoter hypermethylation in both CRC cell lines and primary CRC, with TCF21 methylation being significantly correlated with lymph node invasion. In this study, we further analyze the expression of TCF21 in CRC tissues and investigate the role of TCF21 in CRC in vitro and in vivo. We also explore the possible pathway regulated by TCF21. We thus demonstrate that decreased levels of TCF21 are associated with the pathological stage, clinical stage and lymph node metastasis, indicating a poor prognosis in CRC patients; overexpression of TCF21 inhibits cell proliferation, migration and invasion in the colorectal cell lines HCT116 and HT29. Furthermore, TCF21 functions as a tumor suppressor probably through inactivation of PI3K/AKT signaling and inhibition of MMPs. Our results suggest that enhancement of TCF21 levels may be a potential strategy to facilitate the prevention and treatment of CRC in the clinic. |
format | Online Article Text |
id | pubmed-5359128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53591282017-03-28 TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling Dai, Youyi Duan, Huaxin Duan, Chaojun Zhu, Hong Zhou, Rongrong Pei, Haiping Shen, Liangfang Onco Targets Ther Original Research Colorectal cancer (CRC) has become a major public health problem, ranking as the third most common type of cancer. Our previous study has revealed that TCF21 is frequently silenced by promoter hypermethylation in both CRC cell lines and primary CRC, with TCF21 methylation being significantly correlated with lymph node invasion. In this study, we further analyze the expression of TCF21 in CRC tissues and investigate the role of TCF21 in CRC in vitro and in vivo. We also explore the possible pathway regulated by TCF21. We thus demonstrate that decreased levels of TCF21 are associated with the pathological stage, clinical stage and lymph node metastasis, indicating a poor prognosis in CRC patients; overexpression of TCF21 inhibits cell proliferation, migration and invasion in the colorectal cell lines HCT116 and HT29. Furthermore, TCF21 functions as a tumor suppressor probably through inactivation of PI3K/AKT signaling and inhibition of MMPs. Our results suggest that enhancement of TCF21 levels may be a potential strategy to facilitate the prevention and treatment of CRC in the clinic. Dove Medical Press 2017-03-14 /pmc/articles/PMC5359128/ /pubmed/28352192 http://dx.doi.org/10.2147/OTT.S118151 Text en © 2017 Dai et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Dai, Youyi Duan, Huaxin Duan, Chaojun Zhu, Hong Zhou, Rongrong Pei, Haiping Shen, Liangfang TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling |
title | TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling |
title_full | TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling |
title_fullStr | TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling |
title_full_unstemmed | TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling |
title_short | TCF21 functions as a tumor suppressor in colorectal cancer through inactivation of PI3K/AKT signaling |
title_sort | tcf21 functions as a tumor suppressor in colorectal cancer through inactivation of pi3k/akt signaling |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359128/ https://www.ncbi.nlm.nih.gov/pubmed/28352192 http://dx.doi.org/10.2147/OTT.S118151 |
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