VU University Medical Center, Department of Neurology, Amsterdam, The Netherlands.
Pharmacogenomics. 2011 Mar;12(3):379-95. doi: 10.2217/pgs.10.197.
Central neurotoxicity of chemotherapy is likely to be multifactorial. There are two hypotheses regarding endogenous mechanisms that may be involved, namely the target and the blood-brain barrier transporter hypotheses. Here, we will review candidate genetic determinants for the risk of chemotherapy-induced neurotoxicity, such as polymorphisms involved in the target mechanism. These include polymorphisms in folate metabolizing enzymes and apolipoprotein E, as well as those in blood-brain barrier transporter genes. Currently, the exact role of pharmacogenetics in mechanisms that lead to central neurotoxicity of chemotherapy has not been fully unraveled. Larger, prospective, longitudinal and more uniform studies are needed, with prechemotherapy and follow-up measurements of neuropsychological performance, MRI, PET, genetic profiles and biomarkers relevant for the proposed target and transporter mechanisms.
化疗引起的中枢神经毒性可能是多因素的。关于可能涉及的内源性机制有两种假说,即靶点和血脑屏障转运体假说。在这里,我们将回顾候选遗传决定因素与化疗引起的神经毒性的风险,如涉及靶点机制的多态性。这些包括叶酸代谢酶和载脂蛋白 E 中的多态性,以及血脑屏障转运体基因中的多态性。目前,药物遗传学在导致化疗引起的中枢神经毒性的机制中的确切作用尚未完全阐明。需要进行更大规模、前瞻性、纵向和更统一的研究,对神经心理学表现、MRI、PET、遗传特征和与拟议的靶点和转运体机制相关的生物标志物进行化疗前和随访测量。