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NCAPH plays important roles in human colon cancer

Colon cancer (CC) is one of the major malignancies worldwide, whose pathogenesis is complex and requires the accumulated alteration of multiple genes and signaling pathways. Condensins are multi-protein complexes that play pivotal roles in chromosome assembly and segregation during mitosis, meiosis...

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Autores principales: Yin, Liang, Jiang, Li-Ping, Shen, Qiu-Shuo, Xiong, Qiu-Xia, Zhuo, Xiao, Zhang, Long-Long, Yu, Hai-Jing, Guo, Xiang, Luo, Ying, Dong, Jian, Kong, Qing-Peng, Yang, Cui-Ping, Chen, Yong-Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386579/
https://www.ncbi.nlm.nih.gov/pubmed/28300828
http://dx.doi.org/10.1038/cddis.2017.88
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author Yin, Liang
Jiang, Li-Ping
Shen, Qiu-Shuo
Xiong, Qiu-Xia
Zhuo, Xiao
Zhang, Long-Long
Yu, Hai-Jing
Guo, Xiang
Luo, Ying
Dong, Jian
Kong, Qing-Peng
Yang, Cui-Ping
Chen, Yong-Bin
author_facet Yin, Liang
Jiang, Li-Ping
Shen, Qiu-Shuo
Xiong, Qiu-Xia
Zhuo, Xiao
Zhang, Long-Long
Yu, Hai-Jing
Guo, Xiang
Luo, Ying
Dong, Jian
Kong, Qing-Peng
Yang, Cui-Ping
Chen, Yong-Bin
author_sort Yin, Liang
collection PubMed
description Colon cancer (CC) is one of the major malignancies worldwide, whose pathogenesis is complex and requires the accumulated alteration of multiple genes and signaling pathways. Condensins are multi-protein complexes that play pivotal roles in chromosome assembly and segregation during mitosis, meiosis and even tumorigenesis. Using tissue microarrays by immunohistochemistry and hematoxylin–eosin staining, we found that non-SMC condensin I complex subunit H (NCAPH) in colon cancerous tissues was higher than that in all corresponding adjacent non-cancerous tissues. We then characterized the exact function of the NCAPH in CC. We provided evidences showing that NCAPH is highly expressed in colorectal cancer cell lines comparing with normal human colonic epithelial cells, and identified many NCAPH mutations in CC patients. We found that depletion of NCAPH inhibits CC cell proliferation, migration in vitro and xenograft tumor formation in vivo. Furthermore, NCAPH knockdown promotes cell apoptosis and cell cycle arrest at G2/M phase. Interestingly, the NCAPH high expression in tumor tissues of colon patients had a significantly better prognosis and survival rate than low-expression patients, suggesting that NCAPH high expression promotes colonic cancerous cell proliferation; on the other hand, it may also sensitize these cells responding to chemo- or radio-therapies. Collectively, these findings reveal an important role of NCAPH in CC, indicating that NCAPH could be used as a new therapeutic target in future.
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spelling pubmed-53865792017-04-27 NCAPH plays important roles in human colon cancer Yin, Liang Jiang, Li-Ping Shen, Qiu-Shuo Xiong, Qiu-Xia Zhuo, Xiao Zhang, Long-Long Yu, Hai-Jing Guo, Xiang Luo, Ying Dong, Jian Kong, Qing-Peng Yang, Cui-Ping Chen, Yong-Bin Cell Death Dis Original Article Colon cancer (CC) is one of the major malignancies worldwide, whose pathogenesis is complex and requires the accumulated alteration of multiple genes and signaling pathways. Condensins are multi-protein complexes that play pivotal roles in chromosome assembly and segregation during mitosis, meiosis and even tumorigenesis. Using tissue microarrays by immunohistochemistry and hematoxylin–eosin staining, we found that non-SMC condensin I complex subunit H (NCAPH) in colon cancerous tissues was higher than that in all corresponding adjacent non-cancerous tissues. We then characterized the exact function of the NCAPH in CC. We provided evidences showing that NCAPH is highly expressed in colorectal cancer cell lines comparing with normal human colonic epithelial cells, and identified many NCAPH mutations in CC patients. We found that depletion of NCAPH inhibits CC cell proliferation, migration in vitro and xenograft tumor formation in vivo. Furthermore, NCAPH knockdown promotes cell apoptosis and cell cycle arrest at G2/M phase. Interestingly, the NCAPH high expression in tumor tissues of colon patients had a significantly better prognosis and survival rate than low-expression patients, suggesting that NCAPH high expression promotes colonic cancerous cell proliferation; on the other hand, it may also sensitize these cells responding to chemo- or radio-therapies. Collectively, these findings reveal an important role of NCAPH in CC, indicating that NCAPH could be used as a new therapeutic target in future. Nature Publishing Group 2017-03 2017-03-16 /pmc/articles/PMC5386579/ /pubmed/28300828 http://dx.doi.org/10.1038/cddis.2017.88 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Yin, Liang
Jiang, Li-Ping
Shen, Qiu-Shuo
Xiong, Qiu-Xia
Zhuo, Xiao
Zhang, Long-Long
Yu, Hai-Jing
Guo, Xiang
Luo, Ying
Dong, Jian
Kong, Qing-Peng
Yang, Cui-Ping
Chen, Yong-Bin
NCAPH plays important roles in human colon cancer
title NCAPH plays important roles in human colon cancer
title_full NCAPH plays important roles in human colon cancer
title_fullStr NCAPH plays important roles in human colon cancer
title_full_unstemmed NCAPH plays important roles in human colon cancer
title_short NCAPH plays important roles in human colon cancer
title_sort ncaph plays important roles in human colon cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386579/
https://www.ncbi.nlm.nih.gov/pubmed/28300828
http://dx.doi.org/10.1038/cddis.2017.88
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