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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by pmartino
Group name EquipePM
Item Type Journal Article
Title Inhibition of DDR1-BCR signalling by nilotinib as a new therapeutic strategy for metastatic colorectal cancer
Creator Jeitany et al.
Author Maya Jeitany
Author Cédric Leroy
Author Priscillia Tosti
Author Marie Lafitte
Author Jordy Le Guet
Author Valérie Simon
Author Debora Bonenfant
Author Bruno Robert
Author Fanny Grillet
Author Caroline Mollevi
Author Safia El Messaoudi
Author Amaëlle Otandault
Author Lucile Canterel-Thouennon
Author Muriel Busson
Author Alain R. Thierry
Author Pierre Martineau
Author Julie Pannequin
Author Serge Roche
Author Audrey Sirvent
Abstract The clinical management of metastatic colorectal cancer (mCRC) faces major challenges. Here, we show that nilotinib, a clinically approved drug for chronic myeloid leukaemia, strongly inhibits human CRC cell invasion in vitro and reduces their metastatic potential in intrasplenic tumour mouse models. Nilotinib acts by inhibiting the kinase activity of DDR1, a receptor tyrosine kinase for collagens, which we identified as a RAS-independent inducer of CRC metastasis. Using quantitative phosphoproteomics, we identified BCR as a new DDR1 substrate and demonstrated that nilotinib prevents DDR1-mediated BCR phosphorylation on Tyr177, which is important for maintaining ?-catenin transcriptional activity necessary for tumour cell invasion. DDR1 kinase inhibition also reduced the invasion of patient-derived metastatic and circulating CRC cell lines. Collectively, our results indicate that the targeting DDR1 kinase activity with nilotinib may be beneficial for patients with mCRC.
Publication EMBO molecular medicine
Volume 10
Issue 4
Date Apr 2018
Journal Abbr EMBO Mol Med
Language eng
DOI 10.15252/emmm.201707918
ISSN 1757-4684
Library Catalog PubMed
Call Number IMPACT: 10.293
Extra IMPACT: 10.293 PMID: 29438985 PMCID: PMC5887546
Tags Animals, collagen receptor, colorectal cancer, Colorectal Neoplasms, Discoidin Domain Receptor 1, HCT116 Cells, HEK293 Cells, Humans, invasion, ipam, ligue, mgc, Mice, mpcc, original, pcc, Phosphoproteins, Protein-Tyrosine Kinases, Proto-Oncogene Proteins c-bcr, Pyrimidines, Receptors, Collagen, rhem, rio, Signal Transduction, siric, targeted therapy, top, tyrosine kinase
Date Added 2018/07/20 - 09:35:33
Date Modified 2021/09/01 - 09:38:36
Notes and Attachments Full Text (Attachment)
PubMed entry (Attachment)


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