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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 liaudet-coopman
Group name EquipeELC
Item Type Journal Article
Title TIF1? Suppresses Tumor Progression by Regulating Mitotic Checkpoints and Chromosomal Stability
Creator Pommier et al.
Author Roxane M. Pommier
Author Johann Gout
Author David F. Vincent
Author Lindsay B. Alcaraz
Author Nicolas Chuvin
Author Vanessa Arfi
Author Sylvie Martel
Author Bastien Kaniewski
Author Guillaume Devailly
Author Geneviève Fourel
Author Pascal Bernard
Author Caroline Moyret-Lalle
Author Stéphane Ansieau
Author Alain Puisieux
Author Ulrich Valcourt
Author Stéphanie Sentis
Author Laurent Bartholin
Abstract The transcription accessory factor TIF1?/TRIM33/RFG7/PTC7/Ectodermin functions as a tumor suppressor that promotes development and cellular differentiation. However, its precise function in cancer has been elusive. In the present study, we report that TIF1? inactivation causes cells to accumulate chromosomal defects, a hallmark of cancer, due to attenuations in the spindle assembly checkpoint and the post-mitotic checkpoint. TIF1? deficiency also caused a loss of contact growth inhibition and increased anchorage-independent growth in vitro and in vivo. Clinically, reduced TIF1? expression in human tumors correlated with an increased rate of genomic rearrangements. Overall, our work indicates that TIF1? exerts its tumor-suppressive functions in part by promoting chromosomal stability.
Publication Cancer Research
Volume 75
Issue 20
Pages 4335-4350
Date Oct 15, 2015
Journal Abbr Cancer Res.
Language eng
DOI 10.1158/0008-5472.CAN-14-3426
ISSN 1538-7445
Library Catalog PubMed
Extra PMID: 26282171
Tags Animals, Carcinoma in Situ, Cell Cycle Checkpoints, Cell Line, Tumor, Cell Transformation, Neoplastic, Chromosomal Instability, Disease Models, Animal, Disease Progression, Down-Regulation, Epithelial-Mesenchymal Transition, Gene Expression Regulation, Neoplastic, Gene Silencing, Humans, Mice, Mice, Knockout, Neoplasms, original, Ploidies, Spindle Apparatus, Transcription Factors
Date Added 2019/05/29 - 13:01:35
Date Modified 2019/05/29 - 13:01:48
Notes and Attachments PubMed entry (Attachment)
Texte intégral (Attachment)


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