Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: unknown, P. 157697 - 157697
Published: Nov. 1, 2024
Language: Английский
Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: unknown, P. 157697 - 157697
Published: Nov. 1, 2024
Language: Английский
Chemical Society Reviews, Journal Year: 2024, Volume and Issue: unknown
Published: Jan. 1, 2024
This review provides a comprehensive summary of the dysregulation redox metabolism in cancer cells and advantages latest advances nanomaterial-assisted metabolic regulation therapy.
Language: Английский
Citations
9Biomaterials, Journal Year: 2024, Volume and Issue: 315, P. 122962 - 122962
Published: Nov. 12, 2024
Language: Английский
Citations
5Advanced Materials, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 2, 2025
Higher and richer nutrient requirements are typical features that distinguish tumor cells from AU: cells, ensuring adequate substrates energy sources for cell proliferation migration. Therefore, deprivation strategies based on targeted technologies can induce impaired viability in which more sensitive than normal cells. In this review, nutrients required by related metabolic pathways introduced, anti-tumor developed to target described. addition the nutritional characteristics of other microenvironment (including macrophages, neutrophils, natural killer T cancer-associated fibroblasts) new also summarized. conclusion, recent advances targeting blockade reviewed, challenges prospects these discussed, theoretical significance optimizing clinical application nutrition strategies.
Language: Английский
Citations
0Seminars in Cancer Biology, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Language: Английский
Citations
0Chinese Chemical Letters, Journal Year: 2025, Volume and Issue: unknown, P. 110942 - 110942
Published: Feb. 1, 2025
Language: Английский
Citations
0ACS Nano, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 20, 2025
Pancreatic ductal adenocarcinoma (PDAC) poses significant therapeutic challenges due to excessive hyaluronic acid (HA) accumulation, which impedes drug delivery. Here, we present a targeted approach reduce HA production by specifically silencing glutamine-fructose-6-phosphate aminotransferase 1 (GFAT1), key enzyme of the hexosamine biosynthesis pathway (HBP) in pancreatic cancer cells. An engineered liposomal system for siGFAT1 delivery, PMLip@siGFAT1, characterized macrophage membrane camouflage, LFC131 peptide-mediated targeting, and calcium phosphate (CaP) as core, was designed ensure prolonged circulation, enhanced inflamed vascular endothelial penetration, subsequent effective tumor cell uptake endosomal escape. Consequently, PMLip@siGFAT1 markedly downregulated level PDAC microenvironment, decompressing vasculature weakening stromal barrier, turn improved permeability chemotherapeutics. In combination with Doxil, demonstrated potent antitumor efficacy minimal systemic toxicity. Importantly, unlike PEGPH20 (hyaluronidase), reduced invasiveness, while preserving skeletal muscle integrity. These findings highlight that holds great potential revitalize downregulation strategies delivery efficacy.
Language: Английский
Citations
0Molecular Biomedicine, Journal Year: 2025, Volume and Issue: 6(1)
Published: Feb. 25, 2025
Abstract Pyroptosis is a regulated form of inflammatory cell death in which Gasdermin D (GSDMD) plays central role as the key effector molecule. GSDMD-mediated pyroptosis characterized by complex biological features and considerable heterogeneity its expression, mechanisms, functional outcomes across various tissues, types, pathological microenvironments. This particularly pronounced inflammation-related diseases tumors. In context diseases, GSDMD expression typically upregulated, activation macrophages, neutrophils, T cells, epithelial mitochondria triggers both pyroptotic non-pyroptotic pathways, leading to release pro-inflammatory cytokines exacerbation tissue damage. However, under certain conditions, may also serve protective immune function. The tumors more manner, where it can either promote evasion or, some instances, induce tumor death. As our understanding GSDMD's continues progress, there have been advancements development inhibitors targeting pyroptosis; however, these therapeutic interventions remain preclinical phase. review systematically examines cellular molecular complexities pyroptosis, with particular emphasis on roles cancer. Furthermore, underscores substantial potential target for precision medicine, highlighting promising clinical applications.
Language: Английский
Citations
0Biomacromolecules, Journal Year: 2025, Volume and Issue: unknown
Published: April 8, 2025
Photodynamic therapy (PDT) has emerged as a promising modality for cancer treatment, but its clinical application is constrained by unexpected phototoxicity arising from nonspecific photosensitizer activation and their "always-on" nature. Herein, we developed switchable nanophotosensitizer, poly(cation-π) nanoparticles (NP), which achieves supramolecular assembly through cation-π interactions. By coupling choline cationic moieties with aromatic photosensitizers (ZnPc), the polymer facilitates self-assembly driven interactions NP engineering. Surprisingly, photoactivity of ZnPc was completely quenched upon complexation via interactions, thereby significantly avoiding skin phototoxicity. Upon targeting tumor cells, undergoes GSH-responsive degradation process that weakens leading to spontaneous restoration amplifying immunogenic pyroptosis. In vivo studies demonstrated achieved high inhibition rate 84% while effectively This work provides novel perspective enhancing safety efficacy PDT-based treatment.
Language: Английский
Citations
0Materials Today Bio, Journal Year: 2025, Volume and Issue: unknown, P. 101799 - 101799
Published: April 1, 2025
Language: Английский
Citations
0Frontiers in Bioengineering and Biotechnology, Journal Year: 2025, Volume and Issue: 13
Published: May 1, 2025
Despite the success in exploring various aspects of origination and therapeutic strategies, cancer has remained one most dreadful metabolic disorders due to failure eradicate tumors comprehensively frequent recurrence because acquired resistance drugs. Recently, several advancements have been evidenced fabrication smart nanocarriers encapsulated with multiple components. Several reasons for nanoencapsulation include enhancement bioavailability drugs, precise targetability reduce adverse effects on normal cells, ability enable controlled drug release rates at tumor sites. In addition, these protect cargo from deactivation, responsively delivering it based physiological or pathological characteristics tumors. this review, we present approaches therapy, including organic materials, inorganic components, their composites, as well biomembrane-based strategies. These along practical applications potential treatment, are discussed depth, highlighting advantages disadvantages, aiming reveal ultimate prospects enhancing delivery efficiency targeted therapy.
Language: Английский
Citations
0