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AKT

Epidermal Growth Factor Strongly Affects Epithelial Na+ Transport and Barrier Function in Fetal Alveolar Cells, with Minor Sex-Specific Effects

[Scientific Reports] Scientists analyzed sex-specific fetal distal lung epithelial cells exposed to epidermal growth factor and related ligands with Ussing chambers, RT-qPCR and Western blots.

The COL-4A1 Polypeptide Destroy Endothelial Cells through the TGF-β/PI3K/AKT Pathway

[Scientific Reports] Human umbilical vascular endothelial cells were cultured with or without COL-4A1 and TNF-α. Cell Counting Kit-8, wound-healing, Transwell and tube formation assays were used to evaluate cell proliferation, migration and angiopoiesis.

CRYβB2 Enhances Tumorigenesis through Upregulation of Nucleolin in Triple Negative Breast Cancer

[Oncogene] Researchers reported that the expression of CRYβB2 in breast cancer cells increased stemness, growth, and metastasis. Transcriptomics data revealed that CRYβB2 upregulated genes that were functionally associated with unfolded protein response, oxidative phosphorylation, and DNA repair, while down-regulating genes related to apoptosis.

Blockade of CHRNB2 Signaling with a Therapeutic Monoclonal Antibody Attenuates the Aggressiveness of Gastric Cancer Cells

[Oncogene] Investigators generated gene knockouts through genome editing, performed RNA interference-mediated knockdown of gene expression, and ectopically expressed CHRNB2 in gastric cancer cells.

Inhibition of PHLPP1/2 Phosphatases Rescues Pancreatic β-Cells in Diabetes

[Cell Reports] Researchers identified pleckstrin homology domain leucine-rich repeat protein phosphatases 1 and 2 as phosphatases whose upregulation led to β-cell failure in diabetes.

AKT3-Mediated IWS1 Phosphorylation Promotes the Proliferation of EGFR-Mutant Lung Adenocarcinomas through Cell Cycle-Regulated U2AF2 RNA Splicing

[Nature Communications] Scientists showed that exon 2 inclusion in the U2AF2 mRNA is a cell cycle-dependent process that is regulated by LEDGF/SRSF1 splicing complexes, whose assembly was controlled by the IWS1 phosphorylation-dependent deposition of histone H3K36me3 marks in the body of target genes.

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