Campo Chiara, Da Silva Filho Miguel Inacio, Weinhold Niels, Goldschmidt Hartmut, Hemminki Kari, Merz Maximilian, Försti Asta
Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
Neurochem Res. 2017 Mar;42(3):925-931. doi: 10.1007/s11064-016-2007-9. Epub 2016 Jul 16.
The introduction of proteasome inhibitors in the treatment of multiple myeloma (MM) patients has been a therapeutic success. Peripheral neuropathy (PNP) remains one of the most frequent side-effects experienced by patients who receive these novel agents. Recent investigations on the mechanisms of PNP in patients treated with bortezomib have suggested genetic susceptibility to neurotoxicity. We used data from a genome-wide association study conducted on 646 bortezomib-treated German MM patients to replicate the previously reported associations between single-nucleotide polymorphisms (SNPs) in candidate genes and PNP in MM patients, including 298 SNPs with a nominal significance (p value <0.05). Twelve associations were confirmed at a significance level p value <0.05. The corresponding SNPs are located in genes involved in drug metabolism (ABCC1, ABCC6), development and function of the nervous system (POGZ, NFAT pathway, EDN1), modulation of immune responses (IL17RD, IL10RA) and the NF-κB signaling pathway (PSMB4, BTCR, F2). We systematically investigated functional consequences of those variants using several bioinformatics tools, such as HaploRegV4.1, RegulomeDB and UCSC Genome Browser. Expression quantitative trait loci (eQTL) data suggested that some of the identified SNPs might influence gene expression through a differential recruitment of transcription factors. In conclusion, we confirmed some of the recently reported associations between germline variation and PNP. Elucidating the mechanisms underlying these associations will contribute to the development of new strategies for the prevention or reduction of PNP.
蛋白酶体抑制剂用于治疗多发性骨髓瘤(MM)患者已取得治疗成功。周围神经病变(PNP)仍然是接受这些新型药物治疗的患者最常经历的副作用之一。最近对接受硼替佐米治疗患者的PNP机制进行的研究表明存在对神经毒性的遗传易感性。我们使用了对646例接受硼替佐米治疗的德国MM患者进行的全基因组关联研究数据,以重复先前报道的候选基因单核苷酸多态性(SNP)与MM患者PNP之间的关联,包括298个具有名义显著性(p值<0.05)的SNP。在显著性水平p值<0.05时确认了12种关联。相应的SNP位于参与药物代谢(ABCC1、ABCC6)、神经系统发育和功能(POGZ、NFAT途径、EDN1)、免疫反应调节(IL17RD、IL10RA)以及NF-κB信号通路(PSMB4、BTCR、F2)的基因中。我们使用几种生物信息学工具,如HaploRegV4.1、RegulomeDB和UCSC基因组浏览器,系统地研究了这些变异的功能后果。表达数量性状位点(eQTL)数据表明,一些已鉴定的SNP可能通过转录因子的差异募集影响基因表达。总之,我们证实了一些最近报道的种系变异与PNP之间的关联。阐明这些关联背后的机制将有助于开发预防或减少PNP的新策略。