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LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer

The overactivation of canonical Wnt/β‐catenin pathway and the maintenance of cancer stem cells (CSCs) are essential for the onset and malignant progression of most human cancers. However, their regulatory mechanism in colorectal cancer (CRC) has not yet been well demonstrated. Low‐density lipoprotei...

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Autores principales: Nie, Xiaobo, Liu, Huiyang, Ye, Wenling, Wei, Xiaoyun, Fan, Lili, Ma, Han, Li, Lanqing, Xue, Wanting, Qi, Wenting, Wang, Yan‐Dong, Chen, Wei‐Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831954/
https://www.ncbi.nlm.nih.gov/pubmed/34997691
http://dx.doi.org/10.1111/jcmm.17164
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author Nie, Xiaobo
Liu, Huiyang
Ye, Wenling
Wei, Xiaoyun
Fan, Lili
Ma, Han
Li, Lanqing
Xue, Wanting
Qi, Wenting
Wang, Yan‐Dong
Chen, Wei‐Dong
author_facet Nie, Xiaobo
Liu, Huiyang
Ye, Wenling
Wei, Xiaoyun
Fan, Lili
Ma, Han
Li, Lanqing
Xue, Wanting
Qi, Wenting
Wang, Yan‐Dong
Chen, Wei‐Dong
author_sort Nie, Xiaobo
collection PubMed
description The overactivation of canonical Wnt/β‐catenin pathway and the maintenance of cancer stem cells (CSCs) are essential for the onset and malignant progression of most human cancers. However, their regulatory mechanism in colorectal cancer (CRC) has not yet been well demonstrated. Low‐density lipoprotein receptor‐related protein 5 (LRP5) has been identified as an indispensable co‐receptor with frizzled family members for the canonical Wnt/β‐catenin signal transduction. Herein, we show that activation of LRP5 gene promotes CSCs‐like phenotypes, including tumorigenicity and drug resistance in CRC cells, through activating the canonical Wnt/β‐catenin and IL‐6/STAT3 signalling pathways. Clinically, the expression of LRP5 is upregulated in human CRC tissues and closely associated with clinical stages of patients with CRC. Further analysis showed silencing of endogenous LRP5 gene is sufficient to suppress the CSCs‐like phenotypes of CRC through inhibiting these two pathways. In conclusion, our findings not only reveal a regulatory cross‐talk between canonical Wnt/β‐catenin signalling pathway, IL‐6/STAT3 signalling pathway and CD133‐related stemness that promote the malignant behaviour of CRC, but also provide a valuable target for the diagnosis and treatment of CRC.
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spelling pubmed-88319542022-02-14 LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer Nie, Xiaobo Liu, Huiyang Ye, Wenling Wei, Xiaoyun Fan, Lili Ma, Han Li, Lanqing Xue, Wanting Qi, Wenting Wang, Yan‐Dong Chen, Wei‐Dong J Cell Mol Med Original Articles The overactivation of canonical Wnt/β‐catenin pathway and the maintenance of cancer stem cells (CSCs) are essential for the onset and malignant progression of most human cancers. However, their regulatory mechanism in colorectal cancer (CRC) has not yet been well demonstrated. Low‐density lipoprotein receptor‐related protein 5 (LRP5) has been identified as an indispensable co‐receptor with frizzled family members for the canonical Wnt/β‐catenin signal transduction. Herein, we show that activation of LRP5 gene promotes CSCs‐like phenotypes, including tumorigenicity and drug resistance in CRC cells, through activating the canonical Wnt/β‐catenin and IL‐6/STAT3 signalling pathways. Clinically, the expression of LRP5 is upregulated in human CRC tissues and closely associated with clinical stages of patients with CRC. Further analysis showed silencing of endogenous LRP5 gene is sufficient to suppress the CSCs‐like phenotypes of CRC through inhibiting these two pathways. In conclusion, our findings not only reveal a regulatory cross‐talk between canonical Wnt/β‐catenin signalling pathway, IL‐6/STAT3 signalling pathway and CD133‐related stemness that promote the malignant behaviour of CRC, but also provide a valuable target for the diagnosis and treatment of CRC. John Wiley and Sons Inc. 2022-01-07 2022-02 /pmc/articles/PMC8831954/ /pubmed/34997691 http://dx.doi.org/10.1111/jcmm.17164 Text en © 2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Nie, Xiaobo
Liu, Huiyang
Ye, Wenling
Wei, Xiaoyun
Fan, Lili
Ma, Han
Li, Lanqing
Xue, Wanting
Qi, Wenting
Wang, Yan‐Dong
Chen, Wei‐Dong
LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
title LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
title_full LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
title_fullStr LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
title_full_unstemmed LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
title_short LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
title_sort lrp5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831954/
https://www.ncbi.nlm.nih.gov/pubmed/34997691
http://dx.doi.org/10.1111/jcmm.17164
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