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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 llasorsa
Group name EquipeMY
Item Type Journal Article
Title Vitamin C enhances co-localization of novel TET1 nuclear bodies with both Cajal and PML bodies in colorectal cancer cells
Creator El Osmani et al.
Author Nour El Osmani
Author Corinne Prévostel
Author Laurence Picque Lasorsa
Author Mohammad El Harakeh
Author Zeina Radwan
Author Hiba Mawlawi
Author Marwan El Sabban
Author Margret Shirinian
Author Zeina Dassouki
Abstract Deregulation of ten-eleven Translocation protein 1 (TET1) is commonly reported to induce imbalances in gene expression and subsequently to colorectal cancer development (CRC). On the other hand, vitamin C (VitC) improves the prognosis of colorectal cancer by reprogramming the cancer epigenome and limiting chemotherapeutic drug resistance events. In this study, we aimed to characterize TET1-specific subcellular compartments and evaluate the effect of VitC on TET1 compartmentalization in colonic tumour cells. We demonstrated that TET1 is concentrated in coarse nuclear bodies (NB) and 5-hydroxymethylcytosine (5hmC) in foci in colorectal cancer cells (HCT116, Caco-2, and HT-29). To our knowledge, this is the first report of a novel intracellular localization profile of TET1 and its demethylation marker, 5hmC, in CRC cells. Interestingly, we found that TET1-NBs frequently interacted with Cajal bodies, but not with promyelocytic leukaemia (PML) bodies. In addition, we report that VitC treatment of HCT116 cells induces 5hmC foci biogenesis and triggers 5hmC marks to form active complexes with nuclear body components, including both Cajal and PML proteins. Our data highlight novel NB-concentrating TET1 in CRC cells and demonstrate that VitC modulates TET1-NBs' interactions with other nuclear structures. These findings reveal novel TET1-dependent cellular functions and potentially provide new insights for CRC management.
Publication Epigenetics
Volume 19
Issue 1
Pages 2337142
Date 2024-12
Journal Abbr Epigenetics
Language eng
DOI 10.1080/15592294.2024.2337142
ISSN 1559-2308
Library Catalog PubMed
Extra PMID: 38583183 PMCID: PMC11000620
Tags 5hmC, Ascorbic Acid, Caco-2 Cells, Cajal bodies, Colorectal Neoplasms, CRC, DNA Methylation, Humans, Mixed Function Oxygenases, Nuclear Bodies, partner proteins, PML bodies, Promyelocytic Leukemia Nuclear Bodies, Proto-Oncogene Proteins, TET1, vitamin C, Vitamins
Date Added 2024/10/07 - 16:22:40
Date Modified 2024/10/07 - 16:22:40
Notes and Attachments PubMed entry (Attachment)
Texte intégral (Attachment)


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