Molecular Hydrogen Enhances Proliferation of Cancer Cells That Exhibit Potent Mitochondrial Unfolded Protein Response.
Tomoya HasegawaMikako ItoSatoru HasegawaMasaki TeranishiKoki TakedaShuto NegishiHiroshi NishiwakiJun-Ichi TakedaTyler W LeBaronKinji OhnoPublished in: International journal of molecular sciences (2022)
Molecular hydrogen ameliorates pathological states in a variety of human diseases, animal models, and cell models, but the effects of hydrogen on cancer have been rarely reported. In addition, the molecular mechanisms underlying the effects of hydrogen remain mostly unelucidated. We found that hydrogen enhances proliferation of four out of seven human cancer cell lines (the responders). The proliferation-promoting effects were not correlated with basal levels of cellular reactive oxygen species. Expression profiling of the seven cells showed that the responders have higher gene expression of mitochondrial electron transport chain (ETC) molecules than the non-responders. In addition, the responders have higher mitochondrial mass, higher mitochondrial superoxide, higher mitochondrial membrane potential, and higher mitochondrial spare respiratory capacity than the non-responders. In the responders, hydrogen provoked mitochondrial unfolded protein response (mtUPR). Suppression of cell proliferation by rotenone, an inhibitor of mitochondrial ETC complex I, was rescued by hydrogen in the responders. Hydrogen triggers mtUPR and induces cell proliferation in cancer cells that have high basal and spare mitochondrial ETC activities.
Keyphrases
- oxidative stress
- cell proliferation
- gene expression
- endothelial cells
- signaling pathway
- induced apoptosis
- reactive oxygen species
- endoplasmic reticulum stress
- cell cycle
- papillary thyroid
- small molecule
- bone marrow
- young adults
- mesenchymal stem cells
- single cell
- genome wide
- squamous cell
- cell death
- hydrogen peroxide
- human health
- anti inflammatory