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LRP5 promotes cancer stem cell traits and chemoresistance in colorectal cancer
Authors:Xiaobo Nie,Huiyang Liu,Wenling Ye,Xiaoyun Wei,Lili Fan,Han Ma,Lanqing Li,Wanting Xue,Wenting Qi,Yan‐  Dong Wang,Wei‐  Dong Chen
Affiliation:1. Key Laboratory of Receptors‐Mediated Gene Regulation and Drug Discovery, School of Basic Medical Sciences, People’s Hospital of Hebi, Henan University, Henan China ; 2. State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing China ; 3. Key Laboratory of Molecular Pathology, School of Basic Medical Science, Inner Mongolia Medical University, Inner Mongolia China
Abstract: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.
Keywords:cancer stem cells, canonical Wnt/β    catenin signalling pathway, colorectal cancer, IL‐  6/STAT3   signalling pathway, LRP5
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