Theaflavin and epigallocatechin‐3‐gallate synergistically induce apoptosis through inhibition of PI3K/Akt signaling upon depolymerizing microtubules in HeLa cells

التفاصيل البيبلوغرافية
العنوان: Theaflavin and epigallocatechin‐3‐gallate synergistically induce apoptosis through inhibition of PI3K/Akt signaling upon depolymerizing microtubules in HeLa cells
المؤلفون: Debabrata Ghosh Dastidar, Debasish Nag, Arnab Ganguli, Subhendu Chakrabarty, Amlan Das, Gopal Chakrabarti
المصدر: Journal of Cellular Biochemistry. 120:5987-6003
بيانات النشر: Wiley, 2018.
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Apoptosis, Microtubules, Biochemistry, Antioxidants, Catechin, Polymerization, HeLa, Phosphatidylinositol 3-Kinases, 03 medical and health sciences, 0302 clinical medicine, Tubulin, Microtubule, Animals, Biflavonoids, Humans, Molecular Biology, Protein kinase B, PI3K/AKT/mTOR pathway, Cell Proliferation, Membrane Potential, Mitochondrial, Binding Sites, biology, Chemistry, Goats, food and beverages, Drug Synergism, Cell Biology, biology.organism_classification, Cell biology, G2 Phase Cell Cycle Checkpoints, 030104 developmental biology, Cell culture, 030220 oncology & carcinogenesis, biology.protein, M Phase Cell Cycle Checkpoints, Signal transduction, Proto-Oncogene Proteins c-akt, HeLa Cells, Signal Transduction
الوصف: Theaflavin (TF) and epigallocatechin-3-gallate (EGCG) both have been reported previously as microtubule depolymerizing agents that also have anticancer effects on various cancer cell lines and in animal models. Here, we have applied TF and EGCG in combination on HeLa cells to investigate if they can potentiate each other to improve their anticancer effect in lower doses and the underlying mechanism. We found that TF and EGCG acted synergistically, in lower doses, to inhibit the growth of HeLa cells. We found the combination of 50 µg/mL TF and 20 µg/mL EGCG to be the most effective combination with a combination index of 0.28. The same combination caused larger accumulation of cells in the G 2 /M phase of the cell cycle, potent mitochondrial membrane potential loss, and synergistic augmentation of apoptosis. We have shown that synergistic activity might be due to stronger microtubule depolymerization by simultaneous binding of TF and EGCG at different sites on tubulin: TF binds at vinblastine binding site on tubulin, and EGCG binds near colchicines binding site on tubulin. A detailed mechanistic analysis revealed that stronger microtubule depolymerization caused effective downregulation of PI3K/Akt signaling and potently induced mitochondrial apoptotic signals, which ultimately resulted in the apoptotic death of HeLa cells in a synergistic manner.
تدمد: 1097-4644
0730-2312
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0374be3378a8599dd73e91bb3a31582f
https://doi.org/10.1002/jcb.27886
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....0374be3378a8599dd73e91bb3a31582f
قاعدة البيانات: OpenAIRE