Journal of Trace Elements in Medicine and Biology, Journal Year: 2024, Volume and Issue: 86, P. 127521 - 127521
Published: Sept. 6, 2024
Language: Английский
Journal of Trace Elements in Medicine and Biology, Journal Year: 2024, Volume and Issue: 86, P. 127521 - 127521
Published: Sept. 6, 2024
Language: Английский
Chemico-Biological Interactions, Journal Year: 2025, Volume and Issue: unknown, P. 111368 - 111368
Published: Jan. 1, 2025
Language: Английский
Citations
1The FASEB Journal, Journal Year: 2025, Volume and Issue: 39(1)
Published: Jan. 6, 2025
The activation of acid-sensing ion channel 1a (ASIC1a) in response to extracellular acidification leads an increase calcium influx, thereby exacerbating the degeneration articular chondrocytes rheumatoid arthritis (RA). It has been suggested that inhibition influx could potentially impede chondrocyte ferroptosis. cystine transporter, solute carrier family 7 member 11 (SLC7A11), is recognized as a key regulator Recent studies suggest tumor suppressor gene p53 facilitates induction ferroptosis by suppressing upregulation SLC7A11. This process mediated nuclear factor erythroid 2-related 2 (NRF2), transcription integral maintenance cellular redox homeostasis and regulation inflammatory responses. study aims investigate role ASIC1a RA determine involvement p53/NRF2/SLC7A11 pathway its underlying mechanism. In vitro experiments revealed acidosis induces reduces expression NRF2 SLC7A11 chondrocytes. Moreover, significantly increased protein levels Pifithrin-α (PFN-α), inhibitor, mitigated acidosis-induced restored diminished Furthermore, PcTx-1, inhibited acidification-induced ferroptosis, enhanced NRF2, reduced expression. vivo demonstrated ASIC1a-specific inhibitor PcTx-1 ameliorated histopathological characteristics ankle joints collagen-induced (CIA) mice, decreased expression, These findings may mitigate RA, via pathway.
Language: Английский
Citations
1New discovery., Journal Year: 2025, Volume and Issue: unknown, P. 1 - 12
Published: Feb. 10, 2025
Objective: This study aims to conduct a comprehensive bioinformatic analysis identify pharmacological targets in rectum tissue, rectal cancer and the effects of Salidroside. Methods: Genes associated with cancer, Salidroside were identified using MeSH retrieval from NCBI database screened GeneCards, TCMSP, HERB, ETCM databases. The overlapping genes visualized Venn diagram created on jvenn website. Protein-protein interactions (PPI), Gene Ontology (GO) analysis, Kyoto Encyclopedia Genomes (KEGG) pathway enrichment analyses performed STRING Metascape Results: Bioinformatic several key differentially expressed following treatment. A total 22 intersecting through PPI network revealed top 10 core proteins CytoHubba plugin. GO KEGG highlighted localization degree within signaling pathways. Conclusions: elucidated mechanisms underlying therapeutic providing theoretical foundation for future research.
Language: Английский
Citations
0Pharmacological Research - Natural Products, Journal Year: 2025, Volume and Issue: unknown, P. 100176 - 100176
Published: Feb. 1, 2025
Language: Английский
Citations
0Journal of Advanced Research, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 1, 2024
Language: Английский
Citations
2Experimental Cell Research, Journal Year: 2024, Volume and Issue: 442(2), P. 114222 - 114222
Published: Aug. 29, 2024
Language: Английский
Citations
1Journal of Trace Elements in Medicine and Biology, Journal Year: 2024, Volume and Issue: 86, P. 127521 - 127521
Published: Sept. 6, 2024
Language: Английский
Citations
1