Publications by authors named "J A Santibanez"

The immune and musculoskeletal systems closely interplay in bone repair and regeneration. After bone injury, the body produces high levels of cytokines and signaling molecules to balance bone formation and resorption. Interleukin (IL)-17A, a cytokine expressed early in the inflammatory process, profoundly influences osteoprogenitor cell fate, thereby contributing to bone homeostasis.

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Medicinal mushroom extracts, i.e. their dried biomass, have long been known as sources of bioactive compounds with positive effects on the human health.

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Hydroxyurea (hydroxycarbamide, HU) arrests cells in the S-phase by inhibiting ribonucleotide reductase and DNA synthesis, significantly contributing to the release of nitric oxide (NO). We investigated the involvement of inducible NO synthase (NOS2) in the cytostatic effect of HU using in vitro shRNA-induced knockdown of the NOS2 transcript (NOS2) or a specific NOS2 inhibitor (1400W) in human erythroleukemic HEL92.1.

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Alterations in the actin cytoskeleton correlates to tumor progression and affect critical cellular processes such as adhesion, migration and invasion. Rho-associated coiled-coil-containing protein kinases (ROCK1 and ROCK2), important regulators of the actin cytoskeleton, are frequently overexpressed in various malignancies. The aim of this study was therefore to identify the key structural features of ROCK1/ROCK2 inhibitors using computer-aided drug design (CADD) approaches.

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Article Synopsis
  • Common antimalarials like artemisinins and chloroquine have additional anti-inflammatory, antiviral, and anticancer effects, leading researchers to explore their derivatives for treating hard-to-treat pancreatic cancer.
  • A study found that 4-aminoquinoline derivatives showed strong anticancer activity against pancreatic ductal adenocarcinoma (PDAC) in both cell cultures and a zebrafish model without causing significant toxicity.
  • These compounds induce cancer cell death through mechanisms that increase reactive oxygen species and inhibit autophagy, suggesting they are promising candidates for further research in pancreatic cancer therapy.
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