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| Content Provider | PubMed Central |
|---|---|
| Author | Puvirajesinghe, Tania M. Bertucci, François Jain, Ashish Scerbo, Pierluigi Belotti, Edwige Audebert, Stéphane Michael, Sebbagh Lopez, Marc Brech, Andreas Finetti, Pascal Emmanuelle, Charafe-jauffret Max, Chaffanet Castellano, Rémy Audrey, Restouin Marchetto, Sylvie Collette, Yves Anthony, Gonçalvès Ian, Macara Birnbaum, Daniel Laurent, Kodjabachian Johansen, Terje Borg, Jean-paul |
| Copyright Year | 2016 |
| Abstract | The non-canonical Wnt/planar cell polarity (Wnt/PCP) pathway plays a crucial role in embryonic development. Recent work has linked defects of this pathway to breast cancer aggressiveness and proposed Wnt/PCP signalling as a therapeutic target. Here we show that the archetypal Wnt/PCP protein VANGL2 is overexpressed in basal breast cancers, associated with poor prognosis and implicated in tumour growth. We identify the scaffold p62/SQSTM1 protein as a novel VANGL2-binding partner and show its key role in an evolutionarily conserved VANGL2–p62/SQSTM1–JNK pathway. This proliferative signalling cascade is upregulated in breast cancer patients with shorter survival and can be inactivated in patient-derived xenograft cells by inhibition of the JNK pathway or by disruption of the VANGL2–p62/SQSTM1 interaction. VANGL2–JNK signalling is thus a potential target for breast cancer therapy. |
| Related Links | http://dx.doi.org/10.1038/ncomms10318 |
| Starting Page | 10318 |
| File Format | |
| ISSN | 20411723 |
| e-ISSN | 20411723 |
| Journal | Nature Communications |
| Volume Number | 7 |
| Language | English |
| Publisher | Nature Publishing Group |
| Publisher Date | 2016-01-01 |
| Access Restriction | Open |
| Rights Holder | Nature Publishing Group |
| Subject Keyword | Biochemistry, Genetics and Molecular Biology(all) Physics and Astronomy(all) Chemistry(all) Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry Physics and Astronomy Biochemistry, Genetics and Molecular Biology |
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