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The Role of Purinergic Receptors in Cancer-Induced Bone Pain

Cancer-induced bone pain severely compromises the quality of life of many patients suffering from bone metastasis, as current therapies leave some patients with inadequate pain relief. The recent development of specific animal models has increased the understanding of the molecular and cellular mech...

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Detalles Bibliográficos
Autores principales: Falk, Sarah, Uldall, Maria, Heegaard, Anne-Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469246/
https://www.ncbi.nlm.nih.gov/pubmed/23091774
http://dx.doi.org/10.1155/2012/758181
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author Falk, Sarah
Uldall, Maria
Heegaard, Anne-Marie
author_facet Falk, Sarah
Uldall, Maria
Heegaard, Anne-Marie
author_sort Falk, Sarah
collection PubMed
description Cancer-induced bone pain severely compromises the quality of life of many patients suffering from bone metastasis, as current therapies leave some patients with inadequate pain relief. The recent development of specific animal models has increased the understanding of the molecular and cellular mechanisms underlying cancer-induced bone pain including the involvement of ATP and the purinergic receptors in the progression of the pain state. In nociception, ATP acts as an extracellular messenger to transmit sensory information both at the peripheral site of tissue damage and in the spinal cord. Several of the purinergic receptors have been shown to be important for the development and maintenance of neuropathic and inflammatory pain, and studies have demonstrated the importance of both peripheral and central mechanisms. We here provide an overview of the current literature on the role of purinergic receptors in cancer-induced bone pain with emphasis on some of the difficulties related to studying this complex pain state.
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spelling pubmed-34692462012-10-22 The Role of Purinergic Receptors in Cancer-Induced Bone Pain Falk, Sarah Uldall, Maria Heegaard, Anne-Marie J Osteoporos Review Article Cancer-induced bone pain severely compromises the quality of life of many patients suffering from bone metastasis, as current therapies leave some patients with inadequate pain relief. The recent development of specific animal models has increased the understanding of the molecular and cellular mechanisms underlying cancer-induced bone pain including the involvement of ATP and the purinergic receptors in the progression of the pain state. In nociception, ATP acts as an extracellular messenger to transmit sensory information both at the peripheral site of tissue damage and in the spinal cord. Several of the purinergic receptors have been shown to be important for the development and maintenance of neuropathic and inflammatory pain, and studies have demonstrated the importance of both peripheral and central mechanisms. We here provide an overview of the current literature on the role of purinergic receptors in cancer-induced bone pain with emphasis on some of the difficulties related to studying this complex pain state. Hindawi Publishing Corporation 2012 2012-10-03 /pmc/articles/PMC3469246/ /pubmed/23091774 http://dx.doi.org/10.1155/2012/758181 Text en Copyright © 2012 Sarah Falk et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Falk, Sarah
Uldall, Maria
Heegaard, Anne-Marie
The Role of Purinergic Receptors in Cancer-Induced Bone Pain
title The Role of Purinergic Receptors in Cancer-Induced Bone Pain
title_full The Role of Purinergic Receptors in Cancer-Induced Bone Pain
title_fullStr The Role of Purinergic Receptors in Cancer-Induced Bone Pain
title_full_unstemmed The Role of Purinergic Receptors in Cancer-Induced Bone Pain
title_short The Role of Purinergic Receptors in Cancer-Induced Bone Pain
title_sort role of purinergic receptors in cancer-induced bone pain
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469246/
https://www.ncbi.nlm.nih.gov/pubmed/23091774
http://dx.doi.org/10.1155/2012/758181
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