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Melatonin changes energy metabolism and reduces oncogenic signaling in ovarian cancer cells
Ovarian cancer (OC) adjusts energy metabolism in favor of its progression and dissemination. Because melatonin (Mel) has antitumor actions, we investigated its impact on energy metabolism and kinase signaling in OC cells (SKOV-3 and CAISMOV-24). Cells were divided into control and Mel-treated groups...
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Published in: | Molecular and cellular endocrinology 2024-10, Vol.592, p.112296, Article 112296 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Ovarian cancer (OC) adjusts energy metabolism in favor of its progression and dissemination. Because melatonin (Mel) has antitumor actions, we investigated its impact on energy metabolism and kinase signaling in OC cells (SKOV-3 and CAISMOV-24). Cells were divided into control and Mel-treated groups, in the presence or absence of the antagonist luzindole. There was a decrease in the levels of HIF-1α, G6PDH, GAPDH, PDH, and CS after Mel treatment even in the presence of luzindole in both OC cells. Mel treatment also reduced the activity of OC-related enzymes including PFK-1, G6PDH, LDH, CS, and GS whereas PDH activity was increased. Lactate and glutamine levels dropped after Mel treatment. Mel further promoted a reduction in the concentrations of CREB, JNK, NF-kB, p-38, ERK1/2, AKT, P70S6K, and STAT in both cell lines. Mel reverses Warburg-type metabolism and possibly reduces glutaminolysis, thereby attenuating various oncogenic molecules associated with OC progression and invasion.
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•Melatonin reduces glycolysis and increases pyruvate dehydrogenase activity in OC cells.•Ovarian cancer metabolism-related enzyme activities were altered by melatonin.•Melatonin has a broad impact on reducing key molecules associated with OC progression.•Melatonin reverses Warburg-type metabolism of OC cells in the presence of luzindole. |
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ISSN: | 0303-7207 1872-8057 1872-8057 |
DOI: | 10.1016/j.mce.2024.112296 |