A Mechanistic Understanding of Axon Degeneration in Chemotherapy-Induced Peripheral Neuropathy

被引:155
作者
Fukuda, Yusuke [1 ,2 ]
Li, Yihang [1 ,2 ]
Segal, Rosalind A. [1 ,2 ]
机构
[1] Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
关键词
axon; chemotherapy; CIPN; degeneration; DRG; neuropathy; sensory neuron; Wallerian; DORSAL-ROOT GANGLION; POTENTIAL VANILLOID 1; WALLERIAN DEGENERATION; SENSORY NEUROPATHY; SELF-DESTRUCTION; DROSOPHILA-MELANOGASTER; CAENORHABDITIS-ELEGANS; INDUCED NEUROTOXICITY; MOLECULAR-MECHANISMS; NEUROTROPHIC FACTOR;
D O I
10.3389/fnins.2017.00481
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chemotherapeutic agents cause many short and long term toxic side effects to peripheral nervous system (PNS) that drastically alter quality of life. Chemotherapy-induced peripheral neuropathy (CIPN) is a common and enduring disorder caused by several anti-neoplastic agents. CIPN typically presents with neuropathic pain, numbness of distal extremities, and/or oversensitivity to thermal or mechanical stimuli. This adverse side effect often requires a reduction in chemotherapy dosage or even discontinuation of treatment. Currently there are no effective treatment options for CIPN. While the underlying mechanisms for CIPN are not understood, current data identify a "dying back" axon degeneration of distal nerve endings as the major pathology in this disorder. Therefore, mechanistic understanding of axon degeneration will provide insights into the pathway and molecular players responsible for CIPN. Here, we review recent findings that expand our understanding of the pathogenesis of CIPN and discuss pathways that may be shared with the axonal degeneration that occurs during developmental axon pruning and during injury-induced Wallerian degeneration. These mechanistic insights provide new avenues for development of therapies to prevent or treat CIPN.
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页数:12
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