Reprint

Redox-Active Molecules as Therapeutic Agents

Edited by
June 2022
266 pages
  • ISBN978-3-0365-4381-9 (Hardback)
  • ISBN978-3-0365-4382-6 (PDF)

This book is a reprint of the Special Issue Redox-Active Molecules as Therapeutic Agents that was published in

Biology & Life Sciences
Summary

Oxidative stress and altered redox signaling have been described in a plethora of pathological conditions. Redox-active molecules can thus potentially be used to modulate the etiology/progression of such diseases. Recent advances in molecular biology and pharmacology have strengthened this area of research by providing novel mechanistic insights. This book compiles a collection of 13 articles, covering a range of topics from in vitro studies to clinical research, focused on the potential therapeutic effects of either natural or synthetic compounds, applicable to different redox-related diseases.

Format
  • Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
non-small cell lung cancer; cisplatin; apurinic/apyrimidinic endonuclease 1; E3330; cytotoxicity; apoptosis; migration; invasion; oxidative stress; sildenafil; DNA damage; systemic sclerosis; bioactivity-based assays; cyanidin; metabolomics; Rubus genus; (poly)phenols; yeast-based discovery platform; withanolide; breast cancer; apoptosis; oxidative stress; DNA damage; mitochondrial reactive oxygen species; peroxiredoxin 3; pro-oxidant therapy; thiostrepton; GSH; Cysteamine; N-acetyl cysteine; KEAP1; NRF2; ATF4; adipose-derived mesenchymal stem cell; amniotic membrane-derived mesenchymal stem cell; antioxidants; assisted reproductive technology; conditioned medium; embryo; in vitro culture; in vitro fertilization; oxidative stress; BAPN; breast cancer; cell invasion; EMT; lysyl-oxidase; lysyl-oxidase like 2; metastases; inhibitors; doxorubicin; chemoresistance; oxidative stress; redox signaling; nuclear factor erythroid 2-related factor 2 (Nrf2); cancer therapy; hydrogen sulfide; reactive oxygen species; H2S donors; cardiorenal syndrome; thiosulfate; selenium-enriched Enterococcus faecium; selenium-enriched Streptococcus thermophilus; antioxidant capacity; glutathione reductase; glutathione peroxidase; CD IGS rats; oxidative stress; lactic acid bacteria; verbascoside; hypercholesterolemia; antioxidants; prostate cancer; curcumin; carnosic acid; cell cycle; OxPhos; SGK1; n/a