Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 523, P. 216251 - 216251
Published: Oct. 12, 2024
Language: Английский
Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 523, P. 216251 - 216251
Published: Oct. 12, 2024
Language: Английский
Advanced Science, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 31, 2025
Colorectal cancer (CRC) is highly resistant to ferroptosis, which hinders the application of anti-ferroptosis therapy. Through drug screening, it found that histone deacetylase inhibitor (HDACi) significantly sensitized CRC ferroptosis. The combination HDACi and ferroptosis inducers synergically suppresses growth both in vivo vitro. Mechanically, reduces suppressor protein (FSP1) by promoting its mRNA degradation. Specifically, confirmed specifically targets HDAC1 promotes H3K27ac modification fat mass- obesity-associated gene (FTO) AlkB Homolog 5, RNA Demethylase (ALKBH5), results significant activation FTO ALKBH5. ALKBH5 N6-methyladenosine (m6A) on FSP1 mRNA, leading Crucially, lactylation HDAC1K412 essential for regulation. Both Vorinostat (SAHA) Trichostatin A (TSA) notably diminish comparison other inhibitors, exhibiting a consistent trend increasing susceptibility In conclusion, research reveals decreases sensitize can be promising therapeutic strategy CRC.
Language: Английский
Citations
4Drug Resistance Updates, Journal Year: 2025, Volume and Issue: 81, P. 101215 - 101215
Published: Feb. 26, 2025
Language: Английский
Citations
1Advanced Science, Journal Year: 2024, Volume and Issue: 11(31)
Published: June 18, 2024
Abstract In the treatment of uveal melanoma (UVM), histone deacetylase inhibitors (HDACi) have emerged as a promising epigenetic therapy. However, their clinical efficacy is hindered by suboptimal pharmacokinetics and strong self‐rescue tumor cells. To overcome these limitations, reactive oxygen species (ROS)‐responsive nanoparticles (NPs) are designed that encapsulate HDACi MS‐275 glutamine metabolism inhibitor V‐9302. Upon reaching microenvironment, NPs can disintegrate, thereby releasing to increase level ROS V‐9302 reduce production glutathione (GSH) related self‐rescue. These synergistic effects lead lethal storm induce cell pyroptosis. When combined with programmed death protein 1 monoclonal antibodies ( α ‐PD‐1), facilitate immune infiltration, improving anti‐tumor immunity, converting “immune‐cold” tumors into “immune‐hot” tumors, enhancing memory in mice. The findings present nano‐delivery strategy for co‐delivery therapeutics metabolic inhibitors, which induces pyroptosis cells improves effectiveness chemotherapy immunotherapy.
Language: Английский
Citations
8Advanced Science, Journal Year: 2024, Volume and Issue: 11(44)
Published: Oct. 9, 2024
Abstract Immunotherapy represents a widely employed modality in clinical oncology, leveraging the activation of human immune system to target and eradicate cancer cells tumor tissues via endogenous mechanisms. However, its efficacy remains constrained by inadequate responses within “cold” microenvironment (TME). In this study, multifunctional nanoscale pyroptosis inducer with cascade enzymatic activity (IMZF), comprising superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), glutathione oxidase (GSHO x ), is dissociated acidic glutathione‐rich TME. The vigorous not only generates oxygen (O 2 ) alleviate hypoxia promote M2 M1 macrophage polarization but also yields reactive species (ROS) depletes (GSH) Functioning as an immunogenic cell death (ICD) activator inducer, IMZF synergistically triggers dendritic maturation inflammatory lymphocyte infiltration ICD‐associated pyroptosis, thereby reversing suppression TMEs. Consequently, it exerts inhibitory effects on both primary distal tumors. This platform‐based offers intelligent strategy for effectively overcoming tumors, providing promising avenue advanced immunotherapeutic interventions.
Language: Английский
Citations
7Materials Today Bio, Journal Year: 2025, Volume and Issue: unknown, P. 101745 - 101745
Published: April 1, 2025
Language: Английский
Citations
0Biomedicines, Journal Year: 2025, Volume and Issue: 13(4), P. 950 - 950
Published: April 12, 2025
Immunogenic cell death (ICD) is a promising cancer therapy where dying tumor cells release damage-associated molecular patterns (DAMPs) to activate immune responses. Recent research highlights the critical role of metabolic reprogramming in cells, including Warburg effect, oxidative stress, and lipid metabolism, modulating ICD shaping microenvironment. These changes enhance activation, making tumors more susceptible surveillance. This review explores mechanisms linking mitochondrial endoplasmic reticulum (ER) ferroptosis. It also discusses innovative therapeutic strategies, such as personalized combination therapies, inhibitors, targeted delivery systems, improve efficacy. The future immunotherapy lies integrating activation overcome evasion, with multi-omics approaches microbiome modulation offering new avenues for enhanced treatment outcomes.
Language: Английский
Citations
0Molecular Cancer, Journal Year: 2025, Volume and Issue: 24(1)
Published: May 3, 2025
Pyroptosis is a distinct form of programmed cell death characterized by the rupture membrane and robust inflammatory responses. Increasing evidence suggests that pyroptosis significantly affects tumor microenvironment antitumor immunity releasing damage-associated molecular patterns (DAMPs) pro-inflammatory mediators, thereby establishing it as pivotal target in cancer immunotherapy. This review thoroughly explores mechanisms underlying pyroptosis, with particular focus on inflammasome activation gasdermin family proteins (GSDMs). It examines role pyroptotic reshaping immune (TIME) involving both cells, discusses recent advancements targeting pathways through therapeutic strategies such small molecule modulators, engineered nanocarriers, combinatory treatments checkpoint inhibitors. We also advances future directions to enhance immunotherapy inhibitors, adoptive therapy, vaccines. study suggested offers promising avenue amplify responses surmount resistance existing immunotherapies, potentially leading more efficacious treatments.
Language: Английский
Citations
0Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 523, P. 216251 - 216251
Published: Oct. 12, 2024
Language: Английский
Citations
2