Pan Shuangyue, Cai Yu, Liu Ronghui, Jiang Shuting, Zhao Hongyang, Jiang Jiahong, Lin Zhen, Liu Qian, Lu Hongrui, Liang Shuhui, Fan Weijiao, Chen Xiaochen, Wu Yejing, Wang Fangqian, Chen Zheling, Hu Ronggui, Yang Liu
Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, 310000, China.
Cancer Center, Department of Medical Oncology, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, 310014, China.
Neurosci Bull. 2025 May 14. doi: 10.1007/s12264-025-01398-0.
Chemotherapy-induced peripheral neurotoxicity (CIPN) is a severe dose-limiting adverse event of chemotherapy. Presently, the mechanism underlying the induction of CIPN remains unclear, and no effective treatment is available. In this study, through metabolomics analyses, we found that nab-paclitaxel therapy markedly increased serum serotonin [5-hydroxtryptamine (5-HT)] levels in both cancer patients and mice compared to the respective controls. Furthermore, nab-paclitaxel-treated enterochromaffin (EC) cells showed increased 5-HT synthesis, and serotonin-treated Schwann cells showed damage, as indicated by the activation of CREB3L3/MMP3/FAS signaling. Venlafaxine, an inhibitor of serotonin and norepinephrine reuptake, was found to protect against nerve injury by suppressing the activation of CREB3L3/MMP3/FAS signaling in Schwann cells. Remarkably, venlafaxine was found to significantly alleviate nab-paclitaxel-induced CIPN in patients without affecting the clinical efficacy of chemotherapy. In summary, our study reveals that EC cell-derived 5-HT plays a critical role in nab-paclitaxel-related neurotoxic lesions, and venlafaxine co-administration represents a novel approach to treating chronic cumulative neurotoxicity commonly reported in nab-paclitaxel-based chemotherapy.
化疗引起的周围神经毒性(CIPN)是化疗严重的剂量限制性不良事件。目前,CIPN的诱发机制尚不清楚,且没有有效的治疗方法。在本研究中,通过代谢组学分析,我们发现与各自的对照组相比,纳米白蛋白结合型紫杉醇治疗显著提高了癌症患者和小鼠血清血清素[5-羟色胺(5-HT)]水平。此外,纳米白蛋白结合型紫杉醇处理的肠嗜铬(EC)细胞显示5-HT合成增加,而血清素处理的施万细胞显示出损伤,这通过CREB3L3/MMP3/FAS信号的激活得以体现。文拉法辛是一种血清素和去甲肾上腺素再摄取抑制剂,被发现可通过抑制施万细胞中CREB3L3/MMP3/FAS信号的激活来预防神经损伤。值得注意的是,发现文拉法辛可显著减轻患者中纳米白蛋白结合型紫杉醇诱导的CIPN,而不影响化疗的临床疗效。总之,我们的研究表明,EC细胞衍生的5-HT在纳米白蛋白结合型紫杉醇相关神经毒性损伤中起关键作用,联合使用文拉法辛是一种治疗纳米白蛋白结合型紫杉醇化疗中常见的慢性累积性神经毒性的新方法。