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pancreatic ductal adenocarcinoma

A Low Amino Acid Environment Promotes Cell Macropinocytosis through the YY1-FGD6 Axis in Ras-Mutant Pancreatic Ductal Adenocarcinoma

[Oncogene] Researchers identified a key regulator of macropinocytosis for the survival of tumor cells in a low amino acid environment in pancreatic ductal adenocarcinoma.

De Novo Expression of Gastrokines in Pancreatic Precursor Lesions Impede the Development of Pancreatic Cancer

[Oncogene] Scientists performed the molecular and histological assessment of patient-derived PanINs, tumor tissues and pancreas from mouse models with PDAC, where they noted marked upregulation of gastrokine proteins.

XP-524 Is a Dual-BET/EP300 Inhibitor That Represses Oncogenic KRAS and Potentiates Immune Checkpoint Inhibition in Pancreatic Cancer

[Proceedings of the National Academy of Sciences of the United States of America] Researchers demonstrated that the multispecificity BET/EP300 inhibitor XP-524 has pronounced single-agent efficacy in vitro, in vivo, and ex vivo human PDAC slice cultures, functioning in part by attenuating oncogenic KRAS signaling.

PD-L1 and PD-L2 Expression in Pancreatic Ductal Adenocarcinoma and Their Correlation with Immune Infiltrates and DNA Damage Response Molecules

[Journal of Pathology Clinical Research] The authors investigated the expression of two PD-1 ligands, PD-L1 and PD-L2, in pancreatic ductal adenocarcinoma, analysed their role in survival, and explored their correlation with clinicopathological features, immune infiltration, and DNA damage response molecules.

Matrix Remodeling-Associated Protein 8 Is a Marker of a Subset of Cancer-Associated Fibroblasts in Pancreatic Cancer

[Pathology International] Analysis of MXRA8 expression in human pancreatic ductal adenocarcinoma samples showed that MXRA8 was differentially co-expressed with other cancer-associated fibroblasts markers.

Analysis of the Glyco-Code in Pancreatic Ductal Adenocarcinoma Identifies Glycan-Mediated Immune Regulatory Circuits

[Communications Biology] By analysing publicly available transcriptomic data of patient samples and cell lines, researchers identified here two specific glycan profiles in pancreatic ductal adenocarcinoma that correlated with progression, clinical outcome and epithelial to mesenchymal transition status.

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