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Use of Animal Models in Understanding Cancer-induced Bone Pain

Many common cancers have a propensity to metastasize to bone. Although malignancies often go undetected in their native tissues, bone metastases produce excruciating pain that severely compromises patient quality of life. Cancer-induced bone pain (CIBP) is poorly managed with existing medications, a...

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Detalles Bibliográficos
Autores principales: Slosky, Lauren M, Largent-Milnes, Tally M, Vanderah, Todd W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552039/
https://www.ncbi.nlm.nih.gov/pubmed/26339191
http://dx.doi.org/10.4137/CGM.S21215
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author Slosky, Lauren M
Largent-Milnes, Tally M
Vanderah, Todd W
author_facet Slosky, Lauren M
Largent-Milnes, Tally M
Vanderah, Todd W
author_sort Slosky, Lauren M
collection PubMed
description Many common cancers have a propensity to metastasize to bone. Although malignancies often go undetected in their native tissues, bone metastases produce excruciating pain that severely compromises patient quality of life. Cancer-induced bone pain (CIBP) is poorly managed with existing medications, and its multifaceted etiology remains to be fully elucidated. Novel analgesic targets arise as more is learned about this complex and distinct pain state. Over the past two decades, multiple animal models have been developed to study CIBP’s unique pathology and identify therapeutic targets. Here, we review animal models of CIBP and the mechanistic insights gained as these models evolve. Findings from immunocompromised and immunocompetent host systems are discussed separately to highlight the effect of model choice on outcome. Gaining an understanding of the unique neuromolecular profile of cancer pain through the use of appropriate animal models will aid in the development of more effective therapeutics for CIBP.
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spelling pubmed-45520392015-09-03 Use of Animal Models in Understanding Cancer-induced Bone Pain Slosky, Lauren M Largent-Milnes, Tally M Vanderah, Todd W Cancer Growth Metastasis Review Many common cancers have a propensity to metastasize to bone. Although malignancies often go undetected in their native tissues, bone metastases produce excruciating pain that severely compromises patient quality of life. Cancer-induced bone pain (CIBP) is poorly managed with existing medications, and its multifaceted etiology remains to be fully elucidated. Novel analgesic targets arise as more is learned about this complex and distinct pain state. Over the past two decades, multiple animal models have been developed to study CIBP’s unique pathology and identify therapeutic targets. Here, we review animal models of CIBP and the mechanistic insights gained as these models evolve. Findings from immunocompromised and immunocompetent host systems are discussed separately to highlight the effect of model choice on outcome. Gaining an understanding of the unique neuromolecular profile of cancer pain through the use of appropriate animal models will aid in the development of more effective therapeutics for CIBP. Libertas Academica 2015-08-23 /pmc/articles/PMC4552039/ /pubmed/26339191 http://dx.doi.org/10.4137/CGM.S21215 Text en © 2015 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Review
Slosky, Lauren M
Largent-Milnes, Tally M
Vanderah, Todd W
Use of Animal Models in Understanding Cancer-induced Bone Pain
title Use of Animal Models in Understanding Cancer-induced Bone Pain
title_full Use of Animal Models in Understanding Cancer-induced Bone Pain
title_fullStr Use of Animal Models in Understanding Cancer-induced Bone Pain
title_full_unstemmed Use of Animal Models in Understanding Cancer-induced Bone Pain
title_short Use of Animal Models in Understanding Cancer-induced Bone Pain
title_sort use of animal models in understanding cancer-induced bone pain
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552039/
https://www.ncbi.nlm.nih.gov/pubmed/26339191
http://dx.doi.org/10.4137/CGM.S21215
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