
International Journal of Nanomedicine, Год журнала: 2024, Номер Volume 19, С. 14171 - 14191
Опубликована: Дек. 1, 2024
Язык: Английский
International Journal of Nanomedicine, Год журнала: 2024, Номер Volume 19, С. 14171 - 14191
Опубликована: Дек. 1, 2024
Язык: Английский
International Immunopharmacology, Год журнала: 2025, Номер 149, С. 114229 - 114229
Опубликована: Фев. 10, 2025
Язык: Английский
Процитировано
0Frontiers in Immunology, Год журнала: 2025, Номер 16
Опубликована: Фев. 11, 2025
Ferroptosis, an iron-dependent form of regulated cell death, is characterized by the lethal accumulation lipid peroxides on cellular membranes. It not only inhibits tumor growth but also enhances immunotherapy responses and overcomes drug resistance in cancer therapy. The inhibition cystine-glutamate antiporter, system Xc-, induces ferroptosis. Imidazole ketone erastin (IKE), inhibitor Xc- functional subunit solute carrier family 7 member 11 (SLC7A11), effective metabolically stable inducer ferroptosis with potential vivo applications. However, cells exhibited differential sensitivity to IKE-induced intrinsic factors determining remain be explored improve its efficacy. Bulk RNA-sequencing data from hepatocellular carcinoma (HCC) normal liver tissues were collected Cancer Genome Atlas (TCGA) Genotype-Tissue Expression (GTEx) databases. Differentially expressed genes identified intersected ferroptosis-related (FRGs) listed FerrDb database, yielding identification 13 distinct FRGs. A signature index model (Risk Score) was developed predict HCC prognosis. And SLC7A11 NAD(P)H quinone dehydrogenase 1 (NQO1) as candidate FRGs indicating poor prognosis HCC. Dicoumarol (DIC), NQO1, subsequently employed assess sensitizing effects IKE treatment. In lines subcutaneous xenograft model, combined suppression NQO1 significantly enhanced inhibitory effect inducing conclusion, our findings demonstrate that DIC sensitized Moreover, drugs enhance susceptibility could provide novel therapeutic strategies for treatment
Язык: Английский
Процитировано
0Frontiers in Cellular Neuroscience, Год журнала: 2025, Номер 19
Опубликована: Апрель 7, 2025
Stroke is characterized with high morbidity, mortality and disability all over the world, one of its core pathologies blood-brain barrier (BBB) dysfunction. BBB plays a crucial physiological role in protecting brain tissues maintaining homeostasis central nervous system (CNS). dysfunction serves as key factor development cerebral edema, inflammation, further neurological damage stroke patients. Currently, stem cells their derived exosomes have shown remarkable potential repairing damaged improving function after stroke. Stem repair integrity through anti-inflammatory, antioxidant, angiogenesis regulation intercellular signaling mechanisms, while cell-derived exosomes, natural nanocarriers, enhance therapeutic effect by carrying active substances such proteins, RNAs miRNAs. This review will present latest research advances treatment, well challenges cell source, transplantation timing, dosage, route administration clinical application, aiming to discuss mechanisms for proposes future directions. are expected provide new strategies early diagnosis precise treatment stroke, promote breakthroughs field
Язык: Английский
Процитировано
0Cellular Signalling, Год журнала: 2025, Номер 132, С. 111824 - 111824
Опубликована: Апрель 23, 2025
Язык: Английский
Процитировано
0Journal of Inflammation Research, Год журнала: 2024, Номер Volume 17, С. 9953 - 9973
Опубликована: Ноя. 1, 2024
Sepsis is a life-threatening organ dysfunction caused by dysregulated host response to infection. Endothelial cells (ECs) are an important cell type typically affected in sepsis, resulting compromised barrier function and various forms of regulated death (RCD). However, the precise mechanisms underlying sepsis-induced EC damage remain unclear. This review summarizes recent research progress on factors that may affect permeability RCD ECs under septic conditions, including glycocalyx, damage-associated molecular patterns, ECs, such as apoptosis, pyroptosis, ferroptosis, autophagy. offers insights into endothelial aiming contribute developing small-molecule targeted clinical therapies.
Язык: Английский
Процитировано
0International Journal of Nanomedicine, Год журнала: 2024, Номер Volume 19, С. 14171 - 14191
Опубликована: Дек. 1, 2024
Язык: Английский
Процитировано
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