Department of Anesthesiology, The Second Hospital of Jilin University, Changchun, China.
Department of Anesthesia, Critical Care and Pain Management, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Mol Pain. 2023 Jan-Dec;19:17448069231182235. doi: 10.1177/17448069231182235.
Given that the incidence of cancer is dramatically increasing nowadays, cancer-related neuropathic pain including tumor-related and therapy-related pain gradually attracts more attention from researchers, which basically behaves as a metabolic-neuro-immune disorder with worse clinical outcomes and prognosis. Among various mechanisms of neuropathic pain, the common underlying one is the activation of inflammatory responses around the injured or affected nerve(s). Innate and adaptive immune reactions following nerve injury together contribute to the regulation of pain. On the other hand, the tumor immune microenvironment involving immune cells, as exemplified by lymphocytes, macrophages, neutrophils and dendritic cells, inflammatory mediators as well as tumor metastasis have added additional characteristics for studying the initiation and maintenance of cancer-related neuropathic pain. Of interest, these immune cells in tumor microenvironment exert potent functions in promoting neuropathic pain through different signaling pathways. To this end, this review mainly focuses on the contribution of different types of immune cells to cancer-related neuropathic pain, aims to provide a comprehensive summary of how these immune cells derived from the certain tumor microenvironment participate in the pathogenesis of neuropathic pain. Furthermore, the clarification of roles of various immune cells in different tumor immune microenvironments associated with certain cancers under neuropathic pain states constitutes innovative biology that takes the pain field in a different direction, and thereby provides more opportunities for novel approaches for the prevention and treatment of cancer-related neuropathic pain.
鉴于如今癌症的发病率显著增加,包括肿瘤相关和治疗相关疼痛在内的癌症相关神经性疼痛逐渐引起研究人员的更多关注,其基本表现为一种代谢性-神经-免疫紊乱,临床结局和预后更差。在神经性疼痛的各种机制中,共同的潜在机制是损伤或受影响神经周围炎症反应的激活。神经损伤后的固有和适应性免疫反应共同参与疼痛的调节。另一方面,肿瘤免疫微环境涉及免疫细胞,如淋巴细胞、巨噬细胞、中性粒细胞和树突状细胞、炎症介质以及肿瘤转移,为研究癌症相关神经性疼痛的发生和维持增添了额外的特征。有趣的是,这些肿瘤微环境中的免疫细胞通过不同的信号通路发挥促进神经性疼痛的强大功能。为此,本综述主要关注不同类型的免疫细胞对癌症相关神经性疼痛的贡献,旨在全面总结这些源自特定肿瘤微环境的免疫细胞如何参与神经性疼痛的发病机制。此外,阐明在神经性疼痛状态下与特定癌症相关的不同肿瘤免疫微环境中各种免疫细胞的作用,构成了创新性生物学,使疼痛领域朝着不同的方向发展,从而为癌症相关神经性疼痛的预防和治疗提供了更多的新方法的机会。