4.7 Article

Rewired Cellular Metabolic Profiles in Response to Metformin under Different Oxygen and Nutrient Conditions

Journal

Publisher

MDPI
DOI: 10.3390/ijms23020989

Keywords

metformin; hypoxia; nutrient availability; rewired metabolic activity; oral cancer; dentistry

Funding

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan [17H04420, 18K19629, JP21zf0127001]
  2. Grants-in-Aid for Scientific Research [17H04420, 18K19629] Funding Source: KAKEN

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This study examined the effects of metformin on cell growth, metabolic activities, and nutrient consumption under different oxygen and nutrient conditions. The results showed that the efficacy of metformin was influenced by cell types, oxygen conditions, and nutrient availability. Additionally, metformin was found to induce metabolic switch and may have potential as a combinational therapy.
Metformin is a metabolic disruptor, and its efficacy and effects on metabolic profiles under different oxygen and nutrient conditions remain unclear. Therefore, the present study examined the effects of metformin on cell growth, the metabolic activities and consumption of glucose, glutamine, and pyruvate, and the intracellular ratio of nicotinamide adenine dinucleotide (NAD(+)) and reduced nicotinamide adenine dinucleotide (NADH) under normoxic (21% O-2) and hypoxic (1% O-2) conditions. The efficacy of metformin with nutrient removal from culture media was also investigated. The results obtained show that the efficacy of metformin was closely associated with cell types and environmental factors. Acute exposure to metformin had no effect on lactate production from glucose, glutamine, or pyruvate, whereas long-term exposure to metformin increased the consumption of glucose and pyruvate and the production of lactate in the culture media of HeLa and HaCaT cells as well as the metabolic activity of glucose. The NAD(+)/NADH ratio decreased during growth with metformin regardless of its efficacy. Furthermore, the inhibitory effects of metformin were enhanced in all cell lines following the removal of glucose or pyruvate from culture media. Collectively, the present results reveal that metformin efficacy may be regulated by oxygen conditions and nutrient availability, and indicate the potential of the metabolic switch induced by metformin as combinational therapy.

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