{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Senavirathna L"],"funding":["National Institutes of Health"],"pagination":["1005"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8145644"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["10(5)"],"pubmed_abstract":["Glyceraldehyde-derived advanced glycation end products (AGEs) play an important role in the pathogenesis of many diseases including cancer. Accumulation of intracellular AGEs could stimulate cancer induction and facilitate cancer progression. We evaluated the toxic effect of glyceraldehyde-derived intracellular AGEs on normal and malignant pancreatic ductal cells by assessing the cell viability, toxicity, and oxidative stress, followed by proteomic analysis. Our functional studies showed that pancreatic cancer cells (PANC-1 and MIA PaCa-2) were more resistant to glyceraldehyde treatment compared to normal pancreatic ductal epithelial cells (HPDE), while cytotoxicity effects were observed in all cell types. Furthermore, using <sup>13</sup>C isotopic labeled glyceraldehyde, the proteomic dat"],"journal":["Cells"],"pubmed_title":["Proteomic Investigation of Glyceraldehyde-Derived Intracellular AGEs and Their Potential Influence on Pancreatic Ductal Cells."],"pmcid":["PMC8145644"],"funding_grant_id":["R01CA180949"],"pubmed_authors":["Ma C","Pan S","Senavirathna L","Chen R"],"additional_accession":[]},"is_claimable":false,"name":"Proteomic Investigation of Glyceraldehyde-Derived Intracellular AGEs and Their Potential Influence on Pancreatic Ductal Cells.","description":"Glyceraldehyde-derived advanced glycation end products (AGEs) play an important role in the pathogenesis of many diseases including cancer. Accumulation of intracellular AGEs could stimulate cancer induction and facilitate cancer progression. We evaluated the toxic effect of glyceraldehyde-derived intracellular AGEs on normal and malignant pancreatic ductal cells by assessing the cell viability, toxicity, and oxidative stress, followed by proteomic analysis. Our functional studies showed that pancreatic cancer cells (PANC-1 and MIA PaCa-2) were more resistant to glyceraldehyde treatment compared to normal pancreatic ductal epithelial cells (HPDE), while cytotoxicity effects were observed in all cell types. Furthermore, using <sup>13</sup>C isotopic labeled glyceraldehyde, the proteomic dat","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Apr","modification":"2025-04-22T02:22:45.905Z","creation":"2022-02-10T14:30:50.592Z"},"accession":"S-EPMC8145644","cross_references":{"pubmed":["33923186"],"doi":["10.3390/cells10051005"]}}