KMID : 0620920210530091413
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Experimental & Molecular Medicine 2021 Volume.53 No. 9 p.1413 ~ p.1422
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Melatonin and doxorubicin synergistically enhance apoptosis via autophagy-dependent reduction of AMPK¥á1 transcription in human breast cancer cells
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Tran Quynh Hoa
Hoang Dang Hieu Song Min-Hyeok Choe Won-Chae Kang In-Sug Kim Sung-Soo Ha Joo-Hun
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Abstract
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Doxorubicin is one of the most effective agents used to treat various cancers, including breast cancer, but its usage is limited by the risk of adverse effects, including cardiotoxicity. Melatonin, a natural hormone that functions as a major regulator of circadian rhythms, has been considered a supplemental component for doxorubicin due to its potential to improve its effectiveness. However, the mechanisms and biological targets of the combination of melatonin and doxorubicin with respect to cancer cell death are not well understood. In the present study, we found that melatonin synergized with doxorubicin to induce apoptosis of breast cancer cells by decreasing the expression of AMP-activated protein kinase ¥á1 (AMPK ¥á1), which acts as a critical survival factor for cancer cells. This cotreatment-induced reduction in AMPK¥á1 expression occurred at the transcriptional level via an autophagy-dependent mechanism. The synergistic effects of the combined treatment were evident in many other cancer cell lines, and melatonin was also highly effective in inducing cancer death when combined with other cancer drugs, including cisplatin, 5-fluorouracil, irinotecan, and sorafenib. AMPK¥á1 expression was decreased in all of these cases, suggesting that reducing AMPK¥á1 can be considered an effective method to increase the sensitivity of cancer cells to doxorubicin treatment.
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KEYWORD
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Biochemistry, Diseases
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