Axonal degeneration in chemotherapy-induced peripheral neurotoxicity: clinical and experimental evidence

被引:26
|
作者
Park, Susanna B. [1 ]
Cetinkaya-Fisgin, Aysel [2 ]
Argyriou, Andreas A. [3 ]
Hoeke, Ahmet [2 ]
Cavaletti, Guido [4 ,5 ]
Alberti, Paola [4 ,5 ]
机构
[1] Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Med Sci, Camperdown, NSW, Australia
[2] Johns Hopkins Sch Med, Dept Neurol, Neuromuscular Div, Baltimore, MD USA
[3] Agios Andreas State Gen Hosp Patras, Dept Neurol, Patras, Greece
[4] Univ Milano Bicocca, Expt Neurol Unit, Monza, Italy
[5] Univ Milano Bicocca, Milan Ctr Neurosci, Monza, Italy
来源
关键词
neuropathy; neurophysiology; oncology; INDUCED NEUROPATHY; WALLERIAN DEGENERATION; SENSORY NEUROTOXICITY; NERVE BIOPSY; SARM1; OXALIPLATIN; PACLITAXEL; BORTEZOMIB; VINCRISTINE; THALIDOMIDE;
D O I
10.1136/jnnp-2021-328323
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple pathological mechanisms are involved in the development of chemotherapy-induced peripheral neurotoxicity (CIPN). Recent work has provided insights into the molecular mechanisms underlying chemotherapy-induced axonal degeneration. This review integrates evidence from preclinical and clinical work on the onset, progression and outcome of axonal degeneration in CIPN. We review likely triggers of axonal degeneration in CIPN and highlight evidence of molecular pathways involved in axonal degeneration and their relevance to CIPN, including SARM1-mediated axon degeneration pathway. We identify potential clinical markers of axonal dysfunction to provide early identification of toxicity as well as present potential treatment strategies to intervene in axonal degeneration pathways. A greater understanding of axonal degeneration processes in CIPN will provide important information regarding the development and progression of axonal dysfunction more broadly and will hopefully assist in the development of successful interventions for CIPN and other neurodegenerative disorders.
引用
收藏
页码:962 / 972
页数:11
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