Nicolini Gabriella, Monfrini Marianna, Scuteri Arianna
Experimental Neurology Unit and Milan Center for Neuroscience, Department of Surgery and Translational Medicine, University of Milano-Bicocca, via Cadore 48, 20900 Monza, Italy.
PhD Neuroscience Program, University of Milano-Bicocca, via Cadore 48, 20900 Monza, Italy.
Toxics. 2015 Aug 7;3(3):322-341. doi: 10.3390/toxics3030322.
Chemotherapy-Induced Peripheral Neuropathy (CIPN) is a dose-limiting side effect of several antineoplastic drugs which significantly reduces patients' quality of life. Although different molecular mechanisms have been investigated, CIPN pathobiology has not been clarified yet. It has largely been recognized that Dorsal Root Ganglia are the main targets of chemotherapy and that the longest nerves are the most damaged, together with fast axonal transport. Indeed, this bidirectional cargo-specific transport has a pivotal role in neuronal function and its impairment is involved in several neurodegenerative and neurodevelopmental diseases. Literature data demonstrate that, despite different mechanisms of action, all antineoplastic agents impair the axonal trafficking to some extent and the severity of the neuropathy correlates with the degree of damage on this bidirectional transport. In this paper, we will examine the effect of the main old and new chemotherapeutic drug categories on axonal transport, with the aim of clarifying their potential mechanisms of action, and, if possible, of identifying neuroprotective strategies, based on the knowledge of the alterations induced by each drugs.
化疗诱导的周围神经病变(CIPN)是几种抗肿瘤药物的剂量限制性副作用,会显著降低患者的生活质量。尽管已经研究了不同的分子机制,但CIPN的病理生物学尚未阐明。人们普遍认识到,背根神经节是化疗的主要靶点,最长的神经以及快速轴突运输受到的损伤最为严重。事实上,这种双向货物特异性运输在神经元功能中起关键作用,其受损与多种神经退行性疾病和神经发育疾病有关。文献数据表明,尽管作用机制不同,但所有抗肿瘤药物都会在一定程度上损害轴突运输,神经病变的严重程度与这种双向运输的损伤程度相关。在本文中,我们将研究主要的新旧化疗药物类别对轴突运输的影响,旨在阐明其潜在的作用机制,并在可能的情况下,根据每种药物引起的改变的知识确定神经保护策略。