Tetrahedron Letters, Journal Year: 2024, Volume and Issue: 154, P. 155395 - 155395
Published: Dec. 1, 2024
Language: Английский
Tetrahedron Letters, Journal Year: 2024, Volume and Issue: 154, P. 155395 - 155395
Published: Dec. 1, 2024
Language: Английский
European Journal of Pharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 177300 - 177300
Published: Jan. 1, 2025
Language: Английский
Citations
3Cancer Letters, Journal Year: 2024, Volume and Issue: 587, P. 216680 - 216680
Published: Feb. 10, 2024
Language: Английский
Citations
15Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217458 - 217458
Published: Jan. 1, 2025
Language: Английский
Citations
1Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217522 - 217522
Published: Feb. 1, 2025
Language: Английский
Citations
1Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217448 - 217448
Published: Jan. 1, 2025
Language: Английский
Citations
0Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217454 - 217454
Published: Jan. 1, 2025
Language: Английский
Citations
0Pharmacological Research, Journal Year: 2025, Volume and Issue: unknown, P. 107604 - 107604
Published: Jan. 1, 2025
Language: Английский
Citations
0Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217527 - 217527
Published: Feb. 1, 2025
Language: Английский
Citations
0Molecular Cancer, Journal Year: 2025, Volume and Issue: 24(1)
Published: March 26, 2025
Metabolic reprogramming plays a pivotal role in the development and progression of tumors. Tumor cells rely on glycolysis as their primary energy production pathway effectively utilize biomolecules generated by pentose phosphate (PPP) for efficient biosynthesis. However, 6-phosphogluconate dehydrogenase (6PGD), crucial enzyme PPP, remains unexplored esophageal squamous cell carcinoma (ESCC). In this study, we observed significant upregulation 6PGD expression ESCC tissues, which correlated with an unfavorable prognosis among patients. The experiments demonstrated that knockdown induces oxidative stress suppresses proliferation. Mechanistically, is achieved through AMPK activation subsequent inhibition downstream mTOR phosphorylation. Moreover, physcion has been found to inhibit activity exert its anti-ESCC effect via AMPK/mTOR pathway. Subsequently, conducted both vitro vivo validate anticancer efficacy combining metformin, activator, physcion. results significantly enhanced growth. This study elucidates impact proliferation along underlying molecular mechanisms, highlighting potential therapeutic target ESCC. Furthermore, investigated novel approach improved anti-tumor therapy involving metformin. These findings will contribute new insights clinical treatment strategies while providing theoretical foundation developing targeted therapies.
Language: Английский
Citations
0Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Journal Year: 2025, Volume and Issue: unknown, P. 167859 - 167859
Published: April 1, 2025
Language: Английский
Citations
0