{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Baudu T"],"funding":["INSERM - EFS - Université de Franche Comté","Ministère de l'Education Nationale, de l'Enseignement Supérieur et de la Recherche","Conseil régional de Bourgogne-Franche-Comté","Conseil Régional de Franche-Comté"],"pagination":["1302"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8533616"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["9(10)"],"pubmed_abstract":["EMT is a reversible cellular process that is linked to gene expression reprogramming, which allows for epithelial cells to undergo a phenotypic switch to acquire mesenchymal properties. EMT is associated with cancer progression and cancer therapeutic resistance and it is known that, during the EMT, many stress response pathways, such as autophagy and NMD, are dysregulated. Therefore, our goal was to study the regulation of ATG8 family members (GABARAP, GABARAPL1, LC3B) by the NMD and to identify molecular links between these two cellular processes that are involved in tumor development and metastasis formation. IHC experiments, which were conducted in a cohort of patients presenting lung adenocarcinomas, showed high GABARAPL1 and low UPF1 levels in EMT+ tumors. We observed increased levels"],"journal":["Biomedicines"],"pubmed_title":["The NMD Pathway Regulates GABARAPL1 mRNA during the EMT."],"pmcid":["PMC8533616"],"funding_grant_id":["-"],"pubmed_authors":["Guittaut M","Fraichard A","Peixoto P","Perez V","Hervouet E","Overs A","Millevoi S","Baguet A","Parratte C","Peigney A","Baudu T","Ancion M","Herfs M"],"additional_accession":[]},"is_claimable":false,"name":"The NMD Pathway Regulates GABARAPL1 mRNA during the EMT.","description":"EMT is a reversible cellular process that is linked to gene expression reprogramming, which allows for epithelial cells to undergo a phenotypic switch to acquire mesenchymal properties. EMT is associated with cancer progression and cancer therapeutic resistance and it is known that, during the EMT, many stress response pathways, such as autophagy and NMD, are dysregulated. Therefore, our goal was to study the regulation of ATG8 family members (GABARAP, GABARAPL1, LC3B) by the NMD and to identify molecular links between these two cellular processes that are involved in tumor development and metastasis formation. IHC experiments, which were conducted in a cohort of patients presenting lung adenocarcinomas, showed high GABARAPL1 and low UPF1 levels in EMT+ tumors. We observed increased levels","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Sep","modification":"2025-04-04T09:18:44.852Z","creation":"2025-04-04T09:18:44.852Z"},"accession":"S-EPMC8533616","cross_references":{"pubmed":["34680418"],"doi":["10.3390/biomedicines9101302"]}}