Preclinical and Clinical Evidence of Therapeutic Agents for Paclitaxel-Induced Peripheral Neuropathy.
Takehiro KawashiriMizuki InoueKohei MoriDaisuke KobayashiKeisuke MineSoichiro UshioHibiki KudamatsuMayako UchidaNobuaki EgashiraTakao ShimazoePublished in: International journal of molecular sciences (2021)
Paclitaxel is an essential drug in the chemotherapy of ovarian, non-small cell lung, breast, gastric, endometrial, and pancreatic cancers. However, it frequently causes peripheral neuropathy as a dose-limiting factor. Animal models of paclitaxel-induced peripheral neuropathy (PIPN) have been established. The mechanisms of PIPN development have been elucidated, and many drugs and agents have been proven to have neuroprotective effects in basic studies. In addition, some of these drugs have been validated in clinical studies for their inhibitory PIPN effects. This review summarizes the basic and clinical evidence for therapeutic or prophylactic effects for PIPN. In pre-clinical research, many reports exist of neuropathy inhibitors that target oxidative stress, inflammatory response, ion channels, transient receptor potential (TRP) channels, cannabinoid receptors, and the monoamine nervous system. Alternatively, very few drugs have demonstrated PIPN efficacy in clinical trials. Thus, enhancing translational research to translate pre-clinical research into clinical research is important.
Keyphrases
- diabetic rats
- inflammatory response
- oxidative stress
- drug induced
- clinical trial
- high glucose
- cell therapy
- single cell
- squamous cell carcinoma
- adverse drug
- stem cells
- randomized controlled trial
- immune response
- ischemia reperfusion injury
- locally advanced
- endothelial cells
- climate change
- bone marrow
- lps induced
- open label
- double blind
- cerebral ischemia
- binding protein
- endometrial cancer
- electronic health record