Pathology - Research and Practice, Journal Year: 2024, Volume and Issue: 261, P. 155511 - 155511
Published: July 30, 2024
Language: Английский
Pathology - Research and Practice, Journal Year: 2024, Volume and Issue: 261, P. 155511 - 155511
Published: July 30, 2024
Language: Английский
Molecular Biotechnology, Journal Year: 2024, Volume and Issue: unknown
Published: March 12, 2024
Language: Английский
Citations
4International Journal of Clinical Oncology, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 27, 2025
Language: Английский
Citations
0Gene, Journal Year: 2025, Volume and Issue: unknown, P. 149411 - 149411
Published: March 1, 2025
Language: Английский
Citations
0Gene, Journal Year: 2025, Volume and Issue: unknown, P. 149462 - 149462
Published: April 1, 2025
Language: Английский
Citations
0Critical Reviews in Oncology/Hematology, Journal Year: 2024, Volume and Issue: 196, P. 104275 - 104275
Published: Feb. 1, 2024
Language: Английский
Citations
3Frontiers in Cell and Developmental Biology, Journal Year: 2024, Volume and Issue: 12
Published: Feb. 7, 2024
Ferroptosis, an iron-dependent form of programmed cell death, introduces a novel perspective on cellular demise. This study investigates the regulatory network exosomal non-coding RNAs (ncRNAs), including miRNAs, circRNAs, and lncRNAs, in ferroptosis modulation. The primary goal is to examine pathological roles ferroptosis-related ncRNAs, particularly ischemic reperfusion injuries. research reveals intricate molecular interactions governing interplay between ncRNAs ferroptosis, elucidating their diverse different non-malignant contexts. Attention given impact diseases, cardiac, cerebral, liver, kidney injuries, as well lung, wound, neuronal Beyond theoretical exploration, provides insights into potential therapeutic applications, emphasizing significance mesenchymal stem cells (MSCs)-derived exosomes. Findings underscore pivotal role MSC-derived modulating responses related regulation, introducing cutting-edge dimension. recognition emphasizes importance exosomes crucial mediators with broad implications. Insights unveil promising avenues for targeted interventions, capitalizing providing comprehensive foundation future strategies.
Language: Английский
Citations
3Human Cell, Journal Year: 2024, Volume and Issue: 37(4), P. 1156 - 1169
Published: May 30, 2024
Abstract To explore the effects of β-Sitosterol upon hepatocellular carcinoma cell proliferation, apoptosis, migration, invasion, and epithelial–mesenchymal transition (EMT), to investigate underlying mechanism using network pharmacology. Human lines (Huh-7 HCCLM3) were expose gradient concentrations (5 μg/mL, 10 20 μg/mL). Cell viability proliferation assessed MTT, CCK-8, colony formation, EdU assays.Flow cytometry was employed evaluate cycle apoptosis. Scratch Transwell assays performed, respectively, detect migration invasion. The levels apoptosis-associated proteins (BAX, BCL2, cleaved caspase3) as well EMT-associated (E-cadherin, N-cadherin, Snail, Vimentin) detected in Huh-7 HCCLM3 Western blot analysis. drug target gene for screened via PubChem subsequently evaluated expression GSE112790 dataset. In addition, level glycogen synthase kinase 3 beta (GSK3B) within Cancer Genome Atlas-Liver Hepatocellular Carcinoma (TCGA-LIHC) database analyzed, along with its correlation survival outcomes patients carcinoma. diagnostic efficiency GSK3B by analyzing ROC curve. Subsequently, transfected overexpression vector then treated further validate association between β-Sitosterol. demonstrated a significantly elevated carcinoma, which could predict patients’ impaired prognosis based on GEO dataset TCGA database. inhibitor (CHIR-98014) notably inhibited promoted apoptosis arrest at G0/G1 phase cells. treatment efffects has been found enhance proliferative invasive capabilities Furthermore it observed that overexpression, obsear can partially reverse inhibitory effect hepatocellular. suppressed enhanced inhibiting expression.
Language: Английский
Citations
3Pathology - Research and Practice, Journal Year: 2024, Volume and Issue: 261, P. 155490 - 155490
Published: July 26, 2024
Language: Английский
Citations
3Biogerontology, Journal Year: 2024, Volume and Issue: 26(1)
Published: Nov. 15, 2024
Language: Английский
Citations
3The International Journal of Biochemistry & Cell Biology, Journal Year: 2024, Volume and Issue: 169, P. 106548 - 106548
Published: Feb. 13, 2024
Language: Английский
Citations
2