Hydroxyurea-The Good, the Bad and the Ugly.
Marcelina W MusiałekDorota RybaczekPublished in: Genes (2021)
Hydroxyurea (HU) is mostly referred to as an inhibitor of ribonucleotide reductase (RNR) and as the agent that is commonly used to arrest cells in the S-phase of the cycle by inducing replication stress. It is a well-known and widely used drug, one which has proved to be effective in treating chronic myeloproliferative disorders and which is considered a staple agent in sickle anemia therapy and-recently-a promising factor in preventing cognitive decline in Alzheimer's disease. The reversibility of HU-induced replication inhibition also makes it a common laboratory ingredient used to synchronize cell cycles. On the other hand, prolonged treatment or higher dosage of hydroxyurea causes cell death due to accumulation of DNA damage and oxidative stress. Hydroxyurea treatments are also still far from perfect and it has been suggested that it facilitates skin cancer progression. Also, recent studies have shown that hydroxyurea may affect a larger number of enzymes due to its less specific interaction mechanism, which may contribute to further as-yet unspecified factors affecting cell response. In this review, we examine the actual state of knowledge about hydroxyurea and the mechanisms behind its cytotoxic effects. The practical applications of the recent findings may prove to enhance the already existing use of the drug in new and promising ways.
Keyphrases
- sickle cell disease
- cognitive decline
- dna damage
- oxidative stress
- cell death
- induced apoptosis
- mild cognitive impairment
- skin cancer
- single cell
- cell therapy
- cell cycle arrest
- drug induced
- diabetic rats
- dna repair
- signaling pathway
- emergency department
- mesenchymal stem cells
- cell proliferation
- endoplasmic reticulum stress
- endothelial cells
- replacement therapy
- pi k akt
- heat stress
- stress induced
- heat shock protein