Pharmacology Institute, University of Heidelberg, Im Neuenheimer Feld 366, 69120, Heidelberg, Germany.
J Mol Med (Berl). 2011 Apr;89(4):321-9. doi: 10.1007/s00109-010-0697-z. Epub 2010 Nov 16.
A variety of cancers are accompanied by debilitating pain, which constitutes the primary reason for poor quality of life in cancer patients. There is an urgent demand for the development of specific mechanism-based therapies against cancer pain. Recently, important advances have been made in mechanisms contributing to cancer pain. A notable finding was that the tumor-derived hematopoietic growth factors, granulocyte- and granulocyte-macrophage-colony-stimulating factors (G-CSF/GM-CSF), subserve important functions in the generation of pain hypersensitivity in tumor-affected regions. In this context, their receptors were unexpectedly found on pain-sensing nerves and were observed to be functionally linked to nociceptive sensitization and tumor-induced pain. Here, we review evidence supporting a role for G-/GM-CSF in sensitization of pain-sensing nerves, the underlying signaling pathways and the cross-talk with other pronociceptive cytokines, peptides and modulators derived from immune cells, osteoclasts and tumor cells. These findings hold implications in the therapy of pain in disease states, such as cancer and rheumatoid arthritis.
多种癌症伴随着使人虚弱的疼痛,这是癌症患者生活质量差的主要原因。人们迫切需要开发针对癌症疼痛的特定机制的治疗方法。最近,癌症疼痛相关机制方面取得了重要进展。一个显著的发现是,肿瘤衍生的造血生长因子粒细胞集落刺激因子(G-CSF)/粒细胞-巨噬细胞集落刺激因子(GM-CSF)在肿瘤影响区域产生痛觉过敏方面发挥着重要作用。在这种情况下,它们的受体出人意料地出现在痛觉感受神经上,并被观察到与伤害感受性致敏和肿瘤引起的疼痛功能相关。在这里,我们综述了支持 G-/GM-CSF 在痛觉感受神经敏化中的作用的证据,以及潜在的信号通路,以及与免疫细胞、破骨细胞和肿瘤细胞衍生的其他促伤害性细胞因子、肽和调节剂的交叉对话。这些发现对疾病状态(如癌症和类风湿关节炎)的疼痛治疗具有重要意义。