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The Walker 256 Breast Cancer Cell- Induced Bone Pain Model in Rats

机译:Walker 256乳腺癌细胞诱导的大鼠骨痛模型

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摘要

The majority of patients with terminal breast cancer show signs of bone metastasis, the most common cause of pain in cancer. Clinically available drug treatment options for the relief of cancer-associated bone pain are limited due to either inadequate pain relief and/or dose-limiting side-effects. One of the major hurdles in understanding the mechanism by which breast cancer causes pain after metastasis to the bones is the lack of suitable preclinical models. Until the late twentieth century, all animal models of cancer induced bone pain involved systemic injection of cancer cells into animals, which caused severe deterioration of animal health due to widespread metastasis. In this mini-review we have discussed details of a recently developed and highly efficient preclinical model of breast cancer induced bone pain: Walker 256 cancer cell- induced bone pain in rats. The model involves direct localized injection of cancer cells into a single tibia in rats, which avoids widespread metastasis of cancer cells and hence animals maintain good health throughout the experimental period. This model closely mimics the human pathophysiology of breast cancer induced bone pain and has great potential to aid in the process of drug discovery for treating this intractable pain condition.
机译:大多数晚期乳腺癌患者显示出骨转移的迹象,这是癌症引起疼痛的最常见原因。由于疼痛缓解不足和/或剂量限制的副作用,限制了用于缓解癌症相关的骨痛的临床可用药物治疗选择受到限制。理解乳腺癌转移到骨骼后引起疼痛的机理的主要障碍之一是缺乏合适的临床前模型。直到二十世纪末,所有由癌症引起的骨痛的动物模型都涉及向动物全身注射癌细胞,由于广泛的转移,这导致动物健康严重恶化。在这份小型回顾中,我们讨论了乳腺癌诱发的骨痛的最新开发且高效的临床前模型的详细信息:大鼠Walker 256癌细胞诱发的骨痛。该模型涉及将癌细胞直接局部注射到大鼠的单个胫骨中,避免了癌细胞的广泛转移,因此动物在整个实验期间都保持良好的健康状态。该模型紧密模拟了人类由乳腺癌引起的骨痛的病理生理,并且在治疗这种难治性疼痛的药物开发过程中具有巨大的潜力。

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