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PRMT1-Mediated PGK1 Arginine Methylation Promotes Colorectal Cancer Glycolysis and Tumorigenesis

[Cell Death & Disease] The authors reported that the protein arginine methyltransferase 1 (PRMT1) promoted glycolysis, proliferation, and tumorigenesis in colorectal cancer cells.

Prolonged Culturing of Colonic Epithelial Organoids Derived from Healthy Individuals and Ulcerative Colitis Patients Results in the Decrease of LINE-1 Methylation Level

[Scientific Reports] Researchers reported that long-term culturing of colonic epithelial organoids generated from stem cells of healthy and diseased individuals resulted in decreased nucleotide element 1 (LINE-1) methylation level, when compared to tissue of origin and short-term cultures.

Pro-Tumorigenic Activity of PYCR1 in Gastric Cancer through Regulating the PI3K/AKT Signaling

[Heliyon] Pyrroline-5-carboxylate reductase 1 (PYCR1) expression was manipulated by depletion or overexpression approaches in gastric cancer cells, and these cells were applied to explore the functional roles of PYCR1.

DHCR24 Insufficiency Promotes Vascular Endothelial Cell Senescence and Endothelial Dysfunction via Inhibition of Caveolin-1/ERK Signaling

[The Journals of Gerontology: Series A] Scientists revealed that DHCR24 expression was chronologically decreased in senescent HUVECs and the aortas of aged mice.

2-Desaza-Annomontine (C81) Impedes Angiogenesis Through Reduced VEGFR2 Expression Derived from Inhibition of CDC2-Like Kinases

[Angiogenesis] Researchers showed that C81, a derivative of the plant alkaloid annomontine previously shown to inhibit endothelial inflammation, impeded angiogenesis by inhibiting CDC2-like kinases and WNT/β-catenin signaling.

PM2.5-Induced Premature Senescence in HUVECs Through the SIRT1/PGC-1α/SIRT3 Pathway

[Science Of The Total Environment] Scientists investigated the impact of PM2.5 on vascular endothelial cell senescence and to elucidate the underlying mechanisms. Their findings revealed that PM2.5 exposure led to an increase in senescence-associated β-galactosidase activity and the expression of the cell cycle-blocking proteins P53/P21 and P16 in HUVECs.

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