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趋化因子及其受体参与癌痛的研究进展 被引量:5

Research progress of chemokines and their receptors in cancer pain
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摘要 癌痛是指由于肿瘤压迫神经或者肿瘤直接侵犯组织导致的疼痛,这严重降低了癌症患者的生活质量。大多数癌痛是慢性的,病程3个月以上,疼痛程度通常与肿瘤生长或诊疗情况密切联系。癌痛可以分成伤害感受性疼痛及神经病理性疼痛,前者又区分为躯体痛及内脏痛;后者表现为持续出现痛觉过敏症状,这与外周或中枢神经发生病变有关。目前,关于癌痛的诊治尚缺乏有成效的具体方案。 Chemokines bind to its G-protein-coupled receptors on target cells inducing adjacent responding cells to produce directional chemotaxis. Interaction of chemokines and their receptors in dorsal root ganglion neurons,spinal dorsal horn and brain participates in the generation and maintenance of cancer pain in response to noxious stimuli.Chemokines have been suggested as candidates of cancer pain treatment. This article reviews the research progress of chemokines and their receptors involved in cancer pain.
作者 鲁莹 李勃 王蓉 万琪 曾俊伟 LU Ying;LI Bo;WANG Rong;WAN Qi;ZENG Jun-wei(Department of Physiology,Zunyi Medical University,Zunyi 563000,China)
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2022年第2期364-369,共6页 Chinese Journal of Pathophysiology
基金 国家自然科学基金资助项目(No.31860291) 2018年贵州省教育厅创新群体重大研究项目(黔教合KY字[2018]025)。
关键词 趋化因子 趋化因子受体 癌痛 Chemokines Chemokine receptors Cancer pain
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  • 1Rankin SM. Chemokines and adult bone marrow stem cells [ J]. Immunol Lett,2012,145 (1-2) :47-54. 被引量:1
  • 2Zernecke A, Bot I, Djalali-Talab Y, et al. Protective role of CXC receptor 4/CXC ligand 12 unveils the importance of neutrophils in atherosclerosis [ J ]. Circ Res, 2008,102 (2) :209-217. 被引量:1
  • 3Akhtar S, Gremse F, Kiessling F, et al. CXCL12 promotes the stabilization of atherosclerotic lesions mediated by smooth muscle progenitor cells in Apoe-deficient mice[ J ]. Arterioscler Thromb Vasc Biol,2013,33(4) :679-686. 被引量:1
  • 4Jawien J. The role of an experimental model of atheroscle- rosis : apoE-knockout mice in developing new drugs against atherogenesis[ J]. Curr Pharm Biotechno1,2012,13 ( 13 ) : 2435-2439. 被引量:1
  • 5Balabanian K, Lagane B, Infantino S, et al. The chemo- kine SDF-1/CXCL12 binds to and signals through the or- phan receptor RDC1 in T lymphocytes [ J ]. J Biol Chem, 2005,280 ( 42 ) : 35760 -35766. 被引量:1
  • 6Graham GJ, Locati M, Mantovani A,et al. The biochem- istry and biology of the atypical chemokine receptors [ J ]. Immunol Lett,2012,145 (1-2) :30-38. 被引量:1
  • 7Li X, Zhu M, Penfold ME, et al. Activation of CXCR7 limits atherosclerosis and improves hyperlipidemia by in- creasing cholesterol uptake in adipose tissue [ J ]. Circula- tion, 2014,129 ( 11 ) : 1244-1253. 被引量:1
  • 8Zhang XY, Su C, Cao Z, et al. CXCR7 upregulation is re- quired for early endothelial progenitor cell-mediated endo- thelial repair in patients with hypertension [ J ]. Hyperten- sion, 2014,63(2) :383-389. 被引量:1
  • 9Hu LH, Zhang T, Shao Q, et al. Atorvastatin suppresses oxidized LDL-induced dendritic cell-like differentiation of RAW264.7 cells regulated by the p38 MAPK pathway [ J]. Mol Cell Biochem,2012,371 (1-2) : 105-113. 被引量:1
  • 10Qiu R, Cai A, Dong Y, et al. SDF-1α upregulation by atorvastatin in rats with acute myocardial infarction via ni- tric oxide production confers anti-inflammatory and anti- apoptotic effects [ J ]. J Biomed Sci,2012,19:99. 被引量:1

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