Mechanisms of cancer pain

被引:40
作者
Haroun, Rayan [1 ]
Wood, John N. [1 ]
Sikandar, Shafaq [2 ]
机构
[1] UCL, Wolfson Inst Biomed Res, Div Med, London, England
[2] Queen Mary Univ London, William Harvey Res Inst, Barts & London Sch Med & Dent, London, England
来源
FRONTIERS IN PAIN RESEARCH | 2023年 / 3卷
基金
英国惠康基金;
关键词
pain; dorsal root ganglia; cancer-induced bone pain; chemotherapy associated pain; neuropathy; cancer; sensitisation; NERVE GROWTH-FACTOR; NECROSIS-FACTOR-ALPHA; MU-OPIOID RECEPTOR; KINASE-C-EPSILON; DORSAL-HORN NEURONS; INDUCED BONE PAIN; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ENDOTHELIN-A RECEPTOR; RAT SENSORY NEURONS; MURINE MODEL;
D O I
10.3389/fpain.2022.1030899
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Personalised and targeted interventions have revolutionised cancer treatment and dramatically improved survival rates in recent decades. Nonetheless, effective pain management remains a problem for patients diagnosed with cancer, who continue to suffer from the painful side effects of cancer itself, as well as treatments for the disease. This problem of cancer pain will continue to grow with an ageing population and the rapid advent of more effective therapeutics to treat the disease. Current pain management guidelines from the World Health Organisation are generalised for different pain severities, but fail to address the heterogeneity of mechanisms in patients with varying cancer types, stages of disease and treatment plans. Pain is the most common complaint leading to emergency unit visits by patients with cancer and over one-third of patients that have been diagnosed with cancer will experience under-treated pain. This review summarises preclinical models of cancer pain states, with a particular focus on cancer-induced bone pain and chemotherapy-associated pain. We provide an overview of how preclinical models can recapitulate aspects of pain and sensory dysfunction that is observed in patients with persistent cancer-induced bone pain or neuropathic pain following chemotherapy. Peripheral and central nervous system mechanisms of cancer pain are discussed, along with key cellular and molecular mediators that have been highlighted in animal models of cancer pain. These include interactions between neuronal cells, cancer cells and non-neuronal cells in the tumour microenvironment. Therapeutic targets beyond opioid-based management are reviewed for the treatment of cancer pain.
引用
收藏
页数:20
相关论文
共 243 条
[1]   Bone Metastasis Pain, from the Bench to the Bedside [J].
Aielli, Federica ;
Ponzetti, Marco ;
Rucci, Nadia .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (02)
[2]   Runx2 association with progression of prostate cancer in patients: mechanisms mediating bone osteolysis and osteoblastic metastatic lesions [J].
Akech, J. ;
Wixted, J. J. ;
Bedard, K. ;
van der Deen, M. ;
Hussain, S. ;
Guise, T. A. ;
van Wijnen, A. J. ;
Stein, J. L. ;
Languino, L. R. ;
Altieri, D. C. ;
Pratap, J. ;
Keller, E. ;
Stein, G. S. ;
Lian, J. B. .
ONCOGENE, 2010, 29 (06) :811-821
[3]   Vincristine hyperalgesia in the rat: A model of painful vincristine neuropathy in humans [J].
Aley, KO ;
Reichling, DB ;
Levine, JD .
NEUROSCIENCE, 1996, 73 (01) :259-265
[4]   Protease-activated receptor 2 sensitizes TRPV1 by protein kinase Cε- and A-dependent mechanisms in rats and mice [J].
Amadesi, Silvia ;
Cottrell, Graeme S. ;
Divino, Lorna ;
Chapman, Kevin ;
Grady, Eileen F. ;
Bautista, Francisco ;
Karanjia, Rustum ;
Barajas-Lopez, Carlos ;
Vanner, Stephen ;
Vergnolle, Nathalie ;
Bunnett, Nigel W. .
JOURNAL OF PHYSIOLOGY-LONDON, 2006, 575 (02) :555-571
[5]   Neurolytic Sympathectomy in the Management of Cancer Pain-Time Effect: A Prospective, Randomized Multicenter Study [J].
Amr, Yasser M. ;
Makharita, Mohamed Y. .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2014, 48 (05) :944-U416
[6]   Osteoclast nuclei of myeloma patients show chromosome translocations specific for the myeloma cell clone:: a new type of cancer-host partnership? [J].
Andersen, T. L. ;
Boissy, P. ;
Sondergaard, T. E. ;
Kupisiewicz, K. ;
Plesner, T. ;
Rasmussen, T. ;
Haaber, J. ;
Kolvraa, S. ;
Delaisse, J-M .
JOURNAL OF PATHOLOGY, 2007, 211 (01) :10-17
[7]  
[Anonymous], 1996, CANC PAIN REL GUID O
[8]   NERVE GROWTH-FACTOR PREVENTS TOXIC NEUROPATHY IN MICE [J].
APFEL, SC ;
LIPTON, RB ;
AREZZO, JC ;
KESSLER, JA .
ANNALS OF NEUROLOGY, 1991, 29 (01) :87-90
[9]   CLONING AND EXPRESSION OF A CDNA-ENCODING AN ENDOTHELIN RECEPTOR [J].
ARAI, H ;
HORI, S ;
ARAMORI, I ;
OHKUBO, H ;
NAKANISHI, S .
NATURE, 1990, 348 (6303) :730-732
[10]  
ARGUELLO F, 1988, CANCER RES, V48, P6876