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FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways

Colorectal cancer stem cells (CSCs), characterized by self-renewal ability and high expression of proliferative genes, contribute to the chemoresistance of colorectal cancer (CRC). We aimed to identify the molecular mechanisms underlying CRC chemoresistance through comprehensive bioinformatics scree...

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Autores principales: Huang, Yan-Feng, Niu, Wen-Bo, Hu, Rong, Wang, Ling-Jun, Huang, Zeng-Yan, Ni, Shi-Hao, Wang, Ming-Qing, Yang, Yi, Huang, Yu-Sheng, Feng, Wen-Jun, Xiao, Wei, Zhu, Da-Jian, Xian, Shao-Xiang, Lu, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167373/
https://www.ncbi.nlm.nih.gov/pubmed/30275459
http://dx.doi.org/10.1038/s41389-018-0088-9
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author Huang, Yan-Feng
Niu, Wen-Bo
Hu, Rong
Wang, Ling-Jun
Huang, Zeng-Yan
Ni, Shi-Hao
Wang, Ming-Qing
Yang, Yi
Huang, Yu-Sheng
Feng, Wen-Jun
Xiao, Wei
Zhu, Da-Jian
Xian, Shao-Xiang
Lu, Lu
author_facet Huang, Yan-Feng
Niu, Wen-Bo
Hu, Rong
Wang, Ling-Jun
Huang, Zeng-Yan
Ni, Shi-Hao
Wang, Ming-Qing
Yang, Yi
Huang, Yu-Sheng
Feng, Wen-Jun
Xiao, Wei
Zhu, Da-Jian
Xian, Shao-Xiang
Lu, Lu
author_sort Huang, Yan-Feng
collection PubMed
description Colorectal cancer stem cells (CSCs), characterized by self-renewal ability and high expression of proliferative genes, contribute to the chemoresistance of colorectal cancer (CRC). We aimed to identify the molecular mechanisms underlying CRC chemoresistance through comprehensive bioinformatics screenings and experimental confirmation of gene functions. We found that high expression of FGF1 intracellular binding protein (FIBP) was correlated with chemoresistance and poor prognosis in CRC patients. Therefore, the chemoresistant CRC cell line HCT116-CSC with high expression of the stem cell markers CD44 and CD133 was established for further phenotypic tests. FIBP knockdown inhibited proliferation, enhanced chemotherapy effects, and attenuated the stemness markers of CRC cells in vivo and in vitro. Through RNA-seq and gene set enrichment analysis, we identified cyclin D1 as a key downstream target in FIBP-regulated cell cycle progression and proliferation. Moreover, FIBP bound to GSK3β, inhibited its phosphorylation at Tyr216, and activated β-catenin/TCF/cyclin D1 signaling in HCT116-CSCs. Additional GSK3β knockdown reversed the FIBP silencing-induced inhibition of proliferation and decreased stemness marker expression in HCT116-CSCs. Furthermore, DNA methylation profiling suggested that FIBP regulated the stemness of CRC cells via methylation activity that was dependent on GSK3β but independent of β-catenin signaling. Our data illuminate the potential of FIBP as a novel therapeutic target for treating chemoresistant CRC through inhibition of GSK3β-related signaling.
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spelling pubmed-61673732018-10-03 FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways Huang, Yan-Feng Niu, Wen-Bo Hu, Rong Wang, Ling-Jun Huang, Zeng-Yan Ni, Shi-Hao Wang, Ming-Qing Yang, Yi Huang, Yu-Sheng Feng, Wen-Jun Xiao, Wei Zhu, Da-Jian Xian, Shao-Xiang Lu, Lu Oncogenesis Article Colorectal cancer stem cells (CSCs), characterized by self-renewal ability and high expression of proliferative genes, contribute to the chemoresistance of colorectal cancer (CRC). We aimed to identify the molecular mechanisms underlying CRC chemoresistance through comprehensive bioinformatics screenings and experimental confirmation of gene functions. We found that high expression of FGF1 intracellular binding protein (FIBP) was correlated with chemoresistance and poor prognosis in CRC patients. Therefore, the chemoresistant CRC cell line HCT116-CSC with high expression of the stem cell markers CD44 and CD133 was established for further phenotypic tests. FIBP knockdown inhibited proliferation, enhanced chemotherapy effects, and attenuated the stemness markers of CRC cells in vivo and in vitro. Through RNA-seq and gene set enrichment analysis, we identified cyclin D1 as a key downstream target in FIBP-regulated cell cycle progression and proliferation. Moreover, FIBP bound to GSK3β, inhibited its phosphorylation at Tyr216, and activated β-catenin/TCF/cyclin D1 signaling in HCT116-CSCs. Additional GSK3β knockdown reversed the FIBP silencing-induced inhibition of proliferation and decreased stemness marker expression in HCT116-CSCs. Furthermore, DNA methylation profiling suggested that FIBP regulated the stemness of CRC cells via methylation activity that was dependent on GSK3β but independent of β-catenin signaling. Our data illuminate the potential of FIBP as a novel therapeutic target for treating chemoresistant CRC through inhibition of GSK3β-related signaling. Nature Publishing Group UK 2018-10-02 /pmc/articles/PMC6167373/ /pubmed/30275459 http://dx.doi.org/10.1038/s41389-018-0088-9 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
Huang, Yan-Feng
Niu, Wen-Bo
Hu, Rong
Wang, Ling-Jun
Huang, Zeng-Yan
Ni, Shi-Hao
Wang, Ming-Qing
Yang, Yi
Huang, Yu-Sheng
Feng, Wen-Jun
Xiao, Wei
Zhu, Da-Jian
Xian, Shao-Xiang
Lu, Lu
FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways
title FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways
title_full FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways
title_fullStr FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways
title_full_unstemmed FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways
title_short FIBP knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating GSK3β-related pathways
title_sort fibp knockdown attenuates growth and enhances chemotherapy in colorectal cancer via regulating gsk3β-related pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167373/
https://www.ncbi.nlm.nih.gov/pubmed/30275459
http://dx.doi.org/10.1038/s41389-018-0088-9
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