Clinical Genitourinary Cancer, Journal Year: 2024, Volume and Issue: 23(1), P. 102262 - 102262
Published: Nov. 1, 2024
Language: Английский
Clinical Genitourinary Cancer, Journal Year: 2024, Volume and Issue: 23(1), P. 102262 - 102262
Published: Nov. 1, 2024
Language: Английский
Expert Review of Anticancer Therapy, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 16
Published: Jan. 10, 2025
Introduction Histone modifications are crucial epigenetic mechanisms for regulating gene expression. acetyltransferases and deacetylases (HDACs) catalyze histone acetylation, a process that mediates transcription. Over recent decades, studies have demonstrated targeting acetylation can be effective in cancer treatment, leading to the development approval of several HDAC inhibitors.
Language: Английский
Citations
1Frontiers in Immunology, Journal Year: 2024, Volume and Issue: 15
Published: June 12, 2024
This study seeks to enhance the accuracy and efficiency of clinical diagnosis therapeutic decision-making in hepatocellular carcinoma (HCC), as well optimize assessment immunotherapy response.
Language: Английский
Citations
5Materials Today Communications, Journal Year: 2025, Volume and Issue: unknown, P. 111751 - 111751
Published: Jan. 1, 2025
Language: Английский
Citations
0Medical Oncology, Journal Year: 2025, Volume and Issue: 42(5)
Published: April 4, 2025
Language: Английский
Citations
0Journal of Cellular and Molecular Medicine, Journal Year: 2025, Volume and Issue: 29(9)
Published: May 1, 2025
ABSTRACT Pancreatic cancer is one of the deadliest malignant tumours worldwide. Despite developments in treatments pancreatic cancer, survival rates remain at a low level, and mechanisms underlying aggressive course are not fully understood. VISTA an immune checkpoint has recently become significant target treatment; however, roles development have largely remained unknown. Histone deacetylase inhibitors (HDACi) been reported to reverse epithelial‐mesenchymal transition (EMT) may enhance efficacy anti‐PD‐1 therapy. The PD‐L1/PD‐1 targeted by this therapy shares structural similarity with VISTA. Moreover, combination vorinostat shown significantly reduce tumour growth suppressing transcription factor c‐Myc. Therefore, study, we aim investigate genes that associated EMT explore potential mechanism involving Twist1, proto‐oncogene, cancer. We also sought determine synergistic effects HDACi, vorinostat, Twist1‐siRNA on expression cells’ viability proliferation. Our results revealed Twist1 blockade cells suppresses EMT‐associated compared administered alone. As result, identifying understanding role process crucial step contribute identification new targets for treatment improvement existing strategies.
Language: Английский
Citations
0Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 178, P. 117158 - 117158
Published: July 22, 2024
Language: Английский
Citations
3Pharmacological Research, Journal Year: 2024, Volume and Issue: 208, P. 107377 - 107377
Published: Aug. 28, 2024
The bromodomain and extraterminal domain (BET) family proteins serve as primary readers of acetylated lysine residues play crucial roles in cell proliferation differentiation. Dysregulation BET has been implicated tumorigenesis, making them important therapeutic targets. BET-bromodomain (BD) inhibitors BET-targeting degraders have developed to inhibit proteins. In this study, we found that the inhibitor MS645 exhibited superior antiproliferative activity than including ARV771, AT1, MZ1 dBET1 triple-negative breast cancer (TNBC) cells. Treatment with led dissociation BETs, MED1 RNA polymerase II from E2F1-3 promoter, resulting suppression transcription subsequent inhibition growth TNBC. contrast, while ARV771 displaced chromatin, it did not significantly alter expression. Mechanistically, induced BRD4 depletion at protein level, which markedly increased EGR1 This elevation subsequently recruited septin 2 9 promoters, enhancing promoting rate vitro vivo. Our findings provide valuable insights into differential mechanisms highlight potential developing molecules strategies for
Language: Английский
Citations
2Processes, Journal Year: 2024, Volume and Issue: 12(12), P. 2702 - 2702
Published: Nov. 30, 2024
In recent years, the development of multifunctional hydrogels has gained significant attention due to their potential in various biomedical applications, including antimicrobial, antioxidant, and anticancer therapies. By integrating biocompatible polymers nanoparticles, these can achieve enhanced activity targeted therapeutic effects. this study, carrageenan/2-dimethyl aminoethyl methacrylate/gelatin (CAR/DEMA/Gelt) composite hydrogel was synthesized using microwave radiation specifically for its efficiency enhancing cross-linking promoting uniform nanoparticle dispersion within matrix. Zinc oxide (ZnO) nanoparticles were incorporated into form (CAR/DEMA/Gelt/ZnO) nanocomposite. The characterized FT-IR, FE-SEM, XRD, TGA, EDX, confirming successful structural integrity. nanocomposite exhibited more antimicrobial than against Gram-positive Staphylococcus aureus (S. aureus) Bacillus subtilis (B. subtilis), with inhibition zones 15 mm 16 mm, respectively, while case Gram-negative bacteria, Klebsiella pneumoniae (K. pneumoniae) Escherichia coli (E. coli), 29 19 respectively. addition unicellular fungi, Candida albicans (C. albicans), zone mm. Moreover, showed anti-inflammatory comparable those Indomethacin antioxidant activity, an impressive IC50 value 33.3 ± 0.05 µg/mL. vitro cytotoxicity assays revealed activity. Against MCF-7 breast cancer cell line, CAR/DEMA/Gelt/ZnO 72.5 0.02% viability, which decreased 30.8 0.01% after loading doxorubicin (DOX). Similarly, HepG2 liver free displayed 59.9 0.006% depleted 29.9 0.005% when DOX uploaded. This demonstrates strong as a platform particularly therapy.
Language: Английский
Citations
1Clinical Genitourinary Cancer, Journal Year: 2024, Volume and Issue: 23(1), P. 102262 - 102262
Published: Nov. 1, 2024
Language: Английский
Citations
0