Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Yuheng, Li, Daojiang, Li, Nanpeng, Su, Chen, Yang, Chunxing, Lin, Changwei, Chen, Miao, Wu, Runliu, Li, Xiaorong, Hu, Gui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
_version_ 1783357847528013824
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
work_keys_str_mv AT duyuheng pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT lidaojiang pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT linanpeng pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT suchen pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT yangchunxing pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT linchangwei pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT chenmiao pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT wurunliu pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT lixiaorong pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling
AT hugui pofut1promotescolorectalcancerdevelopmentthroughtheactivationofnotch1signaling