Use of Animal Models in Understanding Cancer-induced Bone Pain.

Cancer growth and metastasis Pub Date : 2015-08-23 eCollection Date: 2015-01-01 DOI:10.4137/CGM.S21215
Lauren M Slosky, Tally M Largent-Milnes, Todd W Vanderah
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引用次数: 44

Abstract

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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利用动物模型了解癌症引起的骨痛。
许多常见的癌症都有向骨转移的倾向。虽然恶性肿瘤通常在其原生组织中未被发现,但骨转移会产生剧烈的疼痛,严重影响患者的生活质量。癌症引起的骨痛(CIBP)在现有的药物治疗中管理不善,其多方面的病因仍有待充分阐明。随着对这种复杂而独特的疼痛状态的了解越来越多,新的镇痛靶点出现了。在过去的二十年中,已经建立了多种动物模型来研究CIBP的独特病理和确定治疗靶点。在这里,我们回顾了CIBP的动物模型以及随着这些模型的发展而获得的机制见解。免疫功能低下和免疫功能正常的宿主系统的研究结果分别进行了讨论,以突出模型选择对结果的影响。通过使用适当的动物模型来了解癌症疼痛的独特神经分子特征将有助于开发更有效的CIBP治疗方法。
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