Affiliation:
1. Research and Development Center of Biomedical Photonics Orel State University Russia
2. Optoelectronics and Measurement Techniques Unit University of Oulu Finland
3. College of Engineering and Physical Sciences Aston University Birmingham UK
4. Orel Regional Clinical Hospital Russia
5. Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology London UK
Abstract
Profound changes in the metabolism of cancer cells have been known for almost 100 years, and many aspects of these changes have continued to be actively studied and discussed. Differences in the results of various studies can be explained by the diversity of tumours, which have differing processes of energy metabolism, and by limitations in the methods used. Here, using fluorescence lifetime needle optical biopsy in a hepatocellular carcinoma (HCC) mouse model and patients with HCC, we measured reduced nicotinamide adenine dinucleotide (NADH) and reduced nicotinamide adenine dinucleotide phosphate (NADPH) in control liver, and in HCC tumours and their adjacent regions. We found that NADH level (mostly responsible for energy metabolism) is increased in tumours but also in adjacent regions of the same liver. NADPH level is significantly decreased in the tumours of patients but increased in the HCC mouse model. However, in the ex vivo tumour slices of mouse HCC, reactive oxygen species production and glutathione level (both dependent on NADPH) were significantly suppressed. Thus, glucose‐dependent NADH and NADPH production in tumours changed but with a more pronounced shift to energy production (NADH), rather than NADPH synthesis for redox balance.
Funder
Ministry of Science and Higher Education of the Russian Federation
Russian Science Foundation