Bioorganic Chemistry, Год журнала: 2025, Номер 160, С. 108441 - 108441
Опубликована: Апрель 5, 2025
Язык: Английский
Bioorganic Chemistry, Год журнала: 2025, Номер 160, С. 108441 - 108441
Опубликована: Апрель 5, 2025
Язык: Английский
Cell Biochemistry and Biophysics, Год журнала: 2025, Номер unknown
Опубликована: Фев. 11, 2025
Язык: Английский
Процитировано
0Frontiers in Immunology, Год журнала: 2025, Номер 16
Опубликована: Фев. 17, 2025
Introduction Macrophages, which tend to aggregate in the hypoxic regions of tissues, have a significant impact on disease progression and outcome because their plastic responsiveness hypoxia, particularly early stages. Understanding macrophages’participation hypoxia-related disorders requires demonstrating acute hypoxia survival, phenotype, function. Methods Here we conducted systematic evaluation macrophage responses over 24 48 h including cell growth activity, inflamatory response, polarization transcriptional metabolic changes. Results We found that suppresses proliferation phagocytosis function with parallel change transcriptome re-programming re-modeling. Although macrophages accumulate heterogeneity based oxygen concentration culture period, genes involved chemotaxis, glycolytic process were commonly altered during hypoxia. Furthermore, pro-inflammatory response was activated concomitantly an enhanced anti-inflammatory regulatory mechanism characterized by increased M2 population metabolite itaconic acid. Aside from glycolysis, key intermediates pentose phosphate pathway significantly increased, such as fructose 1,6-bisphosphate (fold change: 7.8), 6-phosphogluconate 6.1), ribose 5-phosphate 3.9), indicated important compensatory regulation rules for Discussion These findings highlight viability phagocytosis, while modifies metabolome specific inflammatory pathways facilitate adaptation conditions.
Язык: Английский
Процитировано
0International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(4), С. 1752 - 1752
Опубликована: Фев. 19, 2025
Hypoxia-inducible factors (HIFs) are master regulators of cellular responses to low oxygen levels and modulate autophagy, a conserved process essential for maintaining homeostasis. Under hypoxic conditions, HIFs regulate the expression autophagy-related genes influence autophagic flux stress responses. Dysregulated hypoxia-induced autophagy promotes cancer cell survival, metabolism, metastasis, thereby contributing treatment resistance. Targeting HIF-mediated pathways or modulating processes offers potential improve traditional therapies overcome drug Pharmacological inhibitors either alone in combination with other treatments, may disrupt pro-survival mechanisms within tumor microenvironment. Further research is needed elucidate intricate interplay between HIF signaling machinery cells. Understanding these could pave way novel therapeutic strategies enhance outcomes combat This review highlights complex relationship development therapy, offering insights into how targeting patient outcomes.
Язык: Английский
Процитировано
0Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0Bioorganic Chemistry, Год журнала: 2025, Номер 160, С. 108441 - 108441
Опубликована: Апрель 5, 2025
Язык: Английский
Процитировано
0