Mesd Is a Universal Inhibitor of Wnt Coreceptors LRP5 and LRP6 and Blocks Wnt/β-Catenin Signaling in Cancer Cells
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作者:
Lu, Wenyan
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So Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USASo Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USA
Lu, Wenyan
[1
]
Liu, Chia-Chen
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机构:
Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
Washington Univ, Sch Med, Dept Physiol & Cell Biol, St Louis, MO 63110 USASo Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USA
Liu, Chia-Chen
[2
,3
]
Thottassery, Jaideep V.
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机构:
So Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USASo Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USA
Thottassery, Jaideep V.
[1
]
Bu, Guojun
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Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
Washington Univ, Sch Med, Dept Physiol & Cell Biol, St Louis, MO 63110 USASo Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USA
Bu, Guojun
[2
,3
]
Li, Yonghe
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So Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USASo Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USA
Li, Yonghe
[1
]
机构:
[1] So Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Physiol & Cell Biol, St Louis, MO 63110 USA
Mesd is a specialized chaperone for low-density lipoprotein receptor-related protein 5 (LRP5) and LRP6. In our previous studies, we found that Mesd binds to mature LRP6 on the cell surface and blocks the binding of Wnt antagonist Dickkopf-1 (Dkk1) to LRP6. Herein, we demonstrate that Mesd also binds to LRP5 with a high affinity and is a universal inhibitor of LRP5 and LRP6 ligands. Mesd not only blocks binding of Writ antagonists Dkk1 and Sclerostin to LRP5 and LRP6 but also inhibits Wnt3A and Rspondin 1-induced Wnt/beta-catenin signaling in LRP5- and LRP6-expressing cells. We also found that Mesd, Dkk1, and Sclerostin compete with one another for binding to LRP5 and LRP6 at the cell surface. More importantly, we demonstrated that Mesd is able to suppress LRP6 phosphorylation and Wnt/beta-catenin signaling in prostate cancer PC-3 cells and inhibits PC-3 cell proliferation. Our results indicate that recombinant Mesd protein is a useful tool for studying Wnt/beta-catenin signaling on the cell surface and has a potential therapeutic role in Wnt-dependent cancers.
机构:
Columbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USAColumbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USA
Culi, J
;
Mann, RS
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Columbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USAColumbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USA
机构:
Columbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USAColumbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USA
Culi, J
;
Mann, RS
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机构:
Columbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USAColumbia Univ, Ctr Neurobiol & Behav, Dept Biochem & Mol Biophys, New York, NY 10032 USA