Environmental Geochemistry and Health, Journal Year: 2024, Volume and Issue: 47(1)
Published: Dec. 14, 2024
Language: Английский
Environmental Geochemistry and Health, Journal Year: 2024, Volume and Issue: 47(1)
Published: Dec. 14, 2024
Language: Английский
Advances in Clinical Medicine, Journal Year: 2025, Volume and Issue: 15(03), P. 621 - 628
Published: Jan. 1, 2025
Language: Английский
Citations
0MedComm, Journal Year: 2024, Volume and Issue: 5(12)
Published: Nov. 28, 2024
Programmed cell death represents a precisely regulated and active cellular demise, governed by complex network of specific genes proteins. The identification multiple forms programmed has significantly advanced the understanding its intricate mechanisms, as demonstrated in recent studies. A thorough grasp these processes is essential across various biological disciplines study diseases. Nonetheless, despite notable progress, exploration relationship between disease, well clinical application, are still nascent stage. Therefore, further development corresponding therapeutic methods strategies holds substantial potential. Our review provides detailed examination primary mechanisms behind apoptosis, autophagy, necroptosis, pyroptosis, ferroptosis. Following this, discussion delves into functions diseases associated dysregulated death. Finally, we highlight existing potential targets focused on cancers neurodegenerative This aims to summarize latest insights from more reliable approach for transformation.
Language: Английский
Citations
2Scientific Reports, Journal Year: 2024, Volume and Issue: 14(1)
Published: Nov. 7, 2024
The crosstalk between cuproptosis and the tumor immune microenvironment (TIME) is vital during clear cell renal carcinoma (ccRCC) malignant progression. However, underlying molecular mechanisms regulate this cross-talk remain elusive. Through tailored machine learning, we analyze clinical ccRCC data from Cancer Genome Atlas (TCGA) to explore critical factors that interaction among cuproptosis, TIME, We found rhomboid-like 2 (RHBDL2), gene affecting process, might inhibit cuproptosis-related genes (CRGs) promotes progression through Wnt/β-catenin pathway. Next, knocking down RHBDL2 expression increased ferredoxin 1 (FDX1) lipoic acid synthase (LIAS) levels but reduced forkhead box P3 (FOXP3) growth in vivo vitro models. By employing HLY78, pathway activator, rescued of CRGs proliferation metastasis capacity cells with knockdown. Mechanistically, inhibits Abnormal may cause suppressive TIME formation by regulating Treg-cell infiltration, thus triggering escape. In summary, our results indicated an oncogene induces tumorigenesis targeting be novel therapeutic direction for metastatic ccRCC.
Language: Английский
Citations
0Environmental Geochemistry and Health, Journal Year: 2024, Volume and Issue: 47(1)
Published: Dec. 14, 2024
Language: Английский
Citations
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