TY - JOUR
T1 - Preclinical and clinical evidence of therapeutic agents for paclitaxel-induced peripheral neuropathy
AU - Kawashiri, Takehiro
AU - Inoue, Mizuki
AU - Mori, Kohei
AU - Kobayashi, Daisuke
AU - Mine, Keisuke
AU - Ushio, Soichiro
AU - Kudamatsu, Hibiki
AU - Uchida, Mayako
AU - Egashira, Nobuaki
AU - Shimazoe, Takao
N1 - Funding Information:
This work was partly supported by JSPS KAKENHI (JP20K07198) and Fukuoka Public Health Promotion Organization Cancer Research Fund.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/8/2
Y1 - 2021/8/2
N2 - 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.
AB - 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.
KW - Adverse effects
KW - Clinical evidence
KW - Paclitaxel
KW - Peripheral neuropathy
KW - Preclinical data
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U2 - 10.3390/ijms22168733
DO - 10.3390/ijms22168733
M3 - Review article
C2 - 34445439
AN - SCOPUS:85112396371
SN - 1661-6596
VL - 22
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 16
M1 - 8733
ER -