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化疗诱导的周围神经病变(CIPN)管理的新兴方法:C5a/C5aR轴的治疗潜力

Emerging Approaches for the Management of Chemotherapy-Induced Peripheral Neuropathy (CIPN): Therapeutic Potential of the C5a/C5aR Axis.

作者信息

Spera Maria C, Cesta Maria C, Zippoli Mara, Varrassi Giustino, Allegretti Marcello

机构信息

Dompé Farmaceutici SpA, Via Campo di Pile, snc, L'Aquila, Italy.

Dompé Farmaceutici SpA, Via Tommaso De Amicis, 95, Naples, Italy.

出版信息

Pain Ther. 2022 Dec;11(4):1113-1136. doi: 10.1007/s40122-022-00431-8. Epub 2022 Sep 13.

Abstract

Chemotherapy-induced peripheral neuropathy (CIPN) is the most common neurologic complication of chemotherapy, resulting in symptoms like pain, sensory loss, and numbness in the hands and feet that cause lots of uneasiness in patients with cancer. They often suffer from pain so severe that it interrupts the treatment, thus invalidating the entire chemotherapy-based healing process, and significantly reducing their quality of life. In this paper, we underline the role of the complement system in CIPN, highlighting the relevance of the C5a fragment and its receptor C5aR1, whose activation is thought to be involved in triggering a cascade of events that can lead to CIPN onset. Recent experimental data showed the ability of docetaxel and paclitaxel to specifically bind and activate C5aR1, thus shining light on one of the molecular mechanisms by which taxanes may activate a cascade of events leading to neuropathy. According to these new evidence, it was possible to suggest new mechanisms underlying the pathophysiology of CIPN. Hence, the C5a/C5aR1 axis may represent a new target for CIPN treatment, and the use of C5aR1 inhibitors can be proposed as a potential new therapeutic option to manage this high unmet medical need.

摘要

化疗诱导的周围神经病变(CIPN)是化疗最常见的神经并发症,会导致诸如疼痛、感觉丧失以及手脚麻木等症状,给癌症患者带来诸多不适。他们常遭受剧痛,以至于中断治疗,进而使整个基于化疗的治愈过程无效,并显著降低其生活质量。在本文中,我们强调补体系统在CIPN中的作用,突出C5a片段及其受体C5aR1的相关性,其激活被认为参与引发一系列可导致CIPN发病的事件。最近的实验数据表明多西他赛和紫杉醇能够特异性结合并激活C5aR1,从而揭示了紫杉烷类药物可能激活一系列导致神经病变事件的分子机制之一。根据这些新证据,有可能提出CIPN病理生理学的新机制。因此,C5a/C5aR1轴可能代表CIPN治疗的新靶点,并且可以提出使用C5aR1抑制剂作为应对这一高度未满足医疗需求的潜在新治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5209/9633900/745ec0fa597f/40122_2022_431_Fig1_HTML.jpg

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