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Updated: Apr 26, 2026

An Automated Differential Nuclear Staining Assay for Accurate Determination of Mitocan Cytotoxicity
Published on: May 12, 2020
Effect of mitochondrial metabolism-interfering agents on cancer cell mitochondrial function and
Achilleas G Mitrakas1, Dimitra Kalamida, Michael I Koukourakis
1Department of Radiotherapy/Oncology, Radiobiology and Radiopathology Unit, Democritus University of Thrace, Alexandroupolis, Greece.
Abstract:
Abnormal mitochondrial function is common in cancer cells and activates metabolic pathways suppressed in normal tissues. Experimental and clinical studies suggest that mitochondria might serve as targets for novel anticancer therapies. We investigated whether mitochondrial metabolism-interfering agents (MMIAs) available currently in clinical practice affect cancer cell mitochondrial metabolism and synergize with chemotherapy and radiotherapy. Two cancer cell lines A549 (lung cancer) and DU145 (prostate cancer) were treated with a variety of MMIAs (metformin, nimodipine, memantine, oxytetracycline, amiodarone, and sodium azide) and their response was assessed using a resazurin reduction method and confocal microscopy. Focusing on amiodarone and metformin, we investigated their potential sensitizing effect on cancer cells when treated with ionizing radiation, cisplatin, and docetaxel. Resazurin reduction was increased by metformin and decreased by amiodarone at nontoxic concentrations. Amiodarone induced mitochondrial swelling, whereas metformin exerted no apparent effect on their morphology. Amiodarone and metformin exerted a weak radiosensitization effect on A549, whereas a synergetic activity with cisplatin and docetaxel was evident in both cell lines. It can be concluded that amiodarone and metformin, being well-established drugs in clinical practice, constitute two potential drugs for further experimental and clinical evaluation as cancer cell sensitizers to chemotherapy and radiotherapy.
Insights
Metformin and amiodarone, existing drugs, show potential as cancer cell sensitizers. They enhance chemotherapy and radiotherapy effectiveness in lung and prostate cancer cell lines.
Area of Science:
- Oncology
- Mitochondrial Biology
- Pharmacology
Background:
- Mitochondrial dysfunction is a hallmark of cancer, presenting mitochondria as potential therapeutic targets.
- Metabolic pathways in cancer cells differ from normal cells, offering unique intervention opportunities.
Purpose of the Study:
- To evaluate if clinically available mitochondrial metabolism-interfering agents (MMIAs) impact cancer cell mitochondrial metabolism.
- To assess the synergistic effects of MMIAs with chemotherapy and radiotherapy in cancer treatment.
Main Methods:
- Two cancer cell lines (A549, DU145) were treated with various MMIAs (metformin, amiodarone, etc.).
- Resazurin reduction assay and confocal microscopy were used to assess cellular response and mitochondrial morphology.
- Sensitizing effects of amiodarone and metformin with radiation, cisplatin, and docetaxel were investigated.
Main Results:
- Metformin increased, while amiodarone decreased, resazurin reduction at non-toxic concentrations.
- Amiodarone induced mitochondrial swelling; metformin had no significant morphological effect.
- Both agents showed weak radiosensitization but synergistic effects with cisplatin and docetaxel in A549 and DU145 cells.
Conclusions:
- Metformin and amiodarone, established drugs, can sensitize cancer cells to chemotherapy and radiotherapy.
- These agents warrant further investigation as adjuncts in cancer therapy to improve treatment outcomes.
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