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POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling
Copy number variations (CNVs) are key drivers of colorectal cancer (CRC). Our previous studies revealed that protein O-fucosyltransferase 1 (POFUT1) overexpression is driven by CNVs during CRC development. The potential role and underlying mechanisms of POFUT1 in CRC were not investigated. In this s...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155199/ https://www.ncbi.nlm.nih.gov/pubmed/30250219 http://dx.doi.org/10.1038/s41419-018-1055-2 |
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author | Du, Yuheng Li, Daojiang Li, Nanpeng Su, Chen Yang, Chunxing Lin, Changwei Chen, Miao Wu, Runliu Li, Xiaorong Hu, Gui |
author_facet | Du, Yuheng Li, Daojiang Li, Nanpeng Su, Chen Yang, Chunxing Lin, Changwei Chen, Miao Wu, Runliu Li, Xiaorong Hu, Gui |
author_sort | Du, Yuheng |
collection | PubMed |
description | Copy number variations (CNVs) are key drivers of colorectal cancer (CRC). Our previous studies revealed that protein O-fucosyltransferase 1 (POFUT1) overexpression is driven by CNVs during CRC development. The potential role and underlying mechanisms of POFUT1 in CRC were not investigated. In this study, we analyzed the expression of POFUT1 in CRC from cosmic and TCGA databases and confirmed that POFUT1 is highly expressed in CRC. We used well characterized CRC cell lines, including SW620 and HCT116 to establish a model POFUT1 knockdown cell line. Using these cells, we investigated the role of POFUT1 in CRC. Our data revealed that silencing POFUT1 in CRC cells inhibits cell proliferation, decreases cell invasion and migration, arrests cell cycle progression, and stimulates CRC cell apoptosis in vitro. We further demonstrate that POFUT1 silencing dramatically suppresses CRC tumor growth and transplantation in vivo. We additionally reveal new mechanistic insights into the role of POFUT1 during CRC, through demonstrating that POFUT1 silencing inhibits Notch1 signaling. Taken together, our findings demonstrate that POFUT1 is a tumor activating gene during CRC development, which positively regulates CRC tumor progression through activating Notch1. |
format | Online Article Text |
id | pubmed-6155199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61551992018-09-28 POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling Du, Yuheng Li, Daojiang Li, Nanpeng Su, Chen Yang, Chunxing Lin, Changwei Chen, Miao Wu, Runliu Li, Xiaorong Hu, Gui Cell Death Dis Article Copy number variations (CNVs) are key drivers of colorectal cancer (CRC). Our previous studies revealed that protein O-fucosyltransferase 1 (POFUT1) overexpression is driven by CNVs during CRC development. The potential role and underlying mechanisms of POFUT1 in CRC were not investigated. In this study, we analyzed the expression of POFUT1 in CRC from cosmic and TCGA databases and confirmed that POFUT1 is highly expressed in CRC. We used well characterized CRC cell lines, including SW620 and HCT116 to establish a model POFUT1 knockdown cell line. Using these cells, we investigated the role of POFUT1 in CRC. Our data revealed that silencing POFUT1 in CRC cells inhibits cell proliferation, decreases cell invasion and migration, arrests cell cycle progression, and stimulates CRC cell apoptosis in vitro. We further demonstrate that POFUT1 silencing dramatically suppresses CRC tumor growth and transplantation in vivo. We additionally reveal new mechanistic insights into the role of POFUT1 during CRC, through demonstrating that POFUT1 silencing inhibits Notch1 signaling. Taken together, our findings demonstrate that POFUT1 is a tumor activating gene during CRC development, which positively regulates CRC tumor progression through activating Notch1. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155199/ /pubmed/30250219 http://dx.doi.org/10.1038/s41419-018-1055-2 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Du, Yuheng Li, Daojiang Li, Nanpeng Su, Chen Yang, Chunxing Lin, Changwei Chen, Miao Wu, Runliu Li, Xiaorong Hu, Gui POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling |
title | POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling |
title_full | POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling |
title_fullStr | POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling |
title_full_unstemmed | POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling |
title_short | POFUT1 promotes colorectal cancer development through the activation of Notch1 signaling |
title_sort | pofut1 promotes colorectal cancer development through the activation of notch1 signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155199/ https://www.ncbi.nlm.nih.gov/pubmed/30250219 http://dx.doi.org/10.1038/s41419-018-1055-2 |
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