Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 96, P. 105663 - 105663
Published: April 16, 2024
Language: Английский
Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 96, P. 105663 - 105663
Published: April 16, 2024
Language: Английский
Drug Discovery Today, Journal Year: 2023, Volume and Issue: 29(1), P. 103819 - 103819
Published: Nov. 7, 2023
Language: Английский
Citations
27Materials Today Communications, Journal Year: 2023, Volume and Issue: 36, P. 106424 - 106424
Published: June 12, 2023
Language: Английский
Citations
26Journal of Drug Delivery Science and Technology, Journal Year: 2023, Volume and Issue: 86, P. 104745 - 104745
Published: July 7, 2023
Language: Английский
Citations
24Nano-Micro Letters, Journal Year: 2024, Volume and Issue: 16(1)
Published: May 2, 2024
As a new form of regulated cell death, ferroptosis has unraveled the unsolicited theory intrinsic apoptosis resistance by cancer cells. The molecular mechanism depends on induction oxidative stress through excessive reactive oxygen species accumulation and glutathione depletion to damage structural integrity Due their high loading tunability, nanocarriers can escort delivery ferro-therapeutics desired site enhanced permeation or retention effect active targeting. This review shed light necessity iron in growth fascinating features regulating cycle metastasis. Additionally, we discussed ferroptosis-mediated therapy using nanoplatforms chemical basis overcoming barriers therapy.
Language: Английский
Citations
11Journal of Drug Delivery Science and Technology, Journal Year: 2025, Volume and Issue: unknown, P. 106614 - 106614
Published: Jan. 1, 2025
Language: Английский
Citations
1International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(2), P. 664 - 664
Published: Jan. 14, 2025
While 5-fluorouracil (5FU) plays a central role in chemotherapy for colorectal cancer (CRC), resistance to 5FU remains major challenge CRC treatment, and its underlying mechanisms remain unclear. In this study, we investigated the relationship between acquisition, stemness, energy metabolism. Among two cell lines, HT29 cells exhibited glycolytic quiescent properties, while CT26 relied on oxidative phosphorylation (OXPHOS) energy. contrast, 5FU-resistant sublines (HT29R CT26R), developed through continuous exposure low concentrations of 5FU, demonstrated enhanced stemness. This was associated with dominance, proliferation, reduced reactive oxygen species (ROS) production. However, treatment medium-chain fatty acid lauric shifted OXPHOS, reducing increasing ROS levels, inducing death, therefore reversing resistance. These findings suggest that an enhancement stemness reprogramming metabolism play key roles acquiring CRC. reversed resistance, further clinical studies are required.
Language: Английский
Citations
1International Journal of Pharmaceutics, Journal Year: 2024, Volume and Issue: 652, P. 123808 - 123808
Published: Jan. 14, 2024
Language: Английский
Citations
7Drug Resistance Updates, Journal Year: 2024, Volume and Issue: 77, P. 101125 - 101125
Published: Aug. 6, 2024
Language: Английский
Citations
7Asian Journal of Pharmaceutical Sciences, Journal Year: 2023, Volume and Issue: 18(5), P. 100852 - 100852
Published: Sept. 1, 2023
How to effectively transform the pro-oncogenic tumor microenvironments (TME) surrounding a into an anti-tumoral never fails attract people study. Small interfering RNA (siRNA) is considered one of most noteworthy research directions that can regulate gene expression following process known as interference (RNAi). The about siRNA delivery targeting cells and TME has been on rise in recent years. Using drugs silence critical proteins was efficient solutions. However, manufacture system faces three major obstacles, i.e., appropriate cargo protection, accurately targeted delivery, site-specific release. In review, we summarized pharmacological actions remolding TME. addition, strategies combination therapy with remodel are thoroughly discussed. meanwhile, advancements development all clinically investigated commercialized technologies also presented. Ultimately, propose nanoparticle drug may be future focus oncogene therapy. This summary offers thorough analysis roadmap for general readers working field.
Language: Английский
Citations
15Medical Oncology, Journal Year: 2023, Volume and Issue: 40(6)
Published: May 10, 2023
Language: Английский
Citations
14