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    A Wnt-producing niche drives proliferative potential and progression in lung adenocarcinoma

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    Authors
    Tammela, Tuomas
    Xue, Wen
    Jacks, Tyler
    UMass Chan Affiliations
    Department of Molecular, Cell and Cancer Biology
    Program in Molecular Medicine
    RNA Therapeutics Institute
    Document Type
    Journal Article
    Publication Date
    2017-05-18
    Keywords
    Biochemistry, Biophysics, and Structural Biology
    Cell and Developmental Biology
    Genetics and Genomics
    Therapeutics
    
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    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903678/
    Abstract
    The heterogeneity of cellular states in cancer has been linked to drug resistance, cancer progression and the presence of cancer cells with properties of normal tissue stem cells. Secreted Wnt signals maintain stem cells in various epithelial tissues, including in lung development and regeneration. Here we show that mouse and human lung adenocarcinomas display hierarchical features with two distinct subpopulations, one with high Wnt signalling activity and another forming a niche that provides the Wnt ligand. The Wnt responder cells showed increased tumour propagation ability, suggesting that these cells have features of normal tissue stem cells. Genetic perturbation of Wnt production or signalling suppressed tumour progression. Small-molecule inhibitors targeting essential posttranslational modification of Wnt reduced tumour growth and markedly decreased the proliferative potential of lung cancer cells, leading to improved survival of tumour-bearing mice. These results indicate that strategies for disrupting pathways that maintain stem-like and niche cell phenotypes can translate into effective anti-cancer therapies.
    Source

    Nature. 2017 May 18;545(7654):355-359. doi: 10.1038/nature22334. Epub 2017 May 10. Link to article on publisher's site

    DOI
    10.1038/nature22334
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/48799
    PubMed ID
    28489818
    Notes

    Full list of authors omitted for brevity. For full list see article.

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    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1038/nature22334
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