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A mathematical model of bone remodeling dynamics for normal bone cell populations and myeloma bone disease

机译:正常骨细胞群体和骨髓瘤骨疾病的骨重塑动力学数学模型

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摘要

Background Multiple myeloma is a hematologic malignancy associated with the development of a destructive osteolytic bone disease. Results Mathematical models are developed for normal bone remodeling and for the dysregulated bone remodeling that occurs in myeloma bone disease. The models examine the critical signaling between osteoclasts (bone resorption) and osteoblasts (bone formation). The interactions of osteoclasts and osteoblasts are modeled as a system of differential equations for these cell populations, which exhibit stable oscillations in the normal case and unstable oscillations in the myeloma case. In the case of untreated myeloma, osteoclasts increase and osteoblasts decrease, with net bone loss as the tumor grows. The therapeutic effects of targeting both myeloma cells and cells of the bone marrow microenvironment on these dynamics are examined. Conclusions The current model accurately reflects myeloma bone disease and illustrates how treatment approaches may be investigated using such computational approaches. Reviewers This article was reviewed by Ariosto Silva and Mark P. Little.
机译:背景多发性骨髓瘤是与破坏性溶骨性骨病发展相关的血液系统恶性肿瘤。结果建立了数学模型,用于正常的骨骼重塑和发生在骨髓瘤骨病中的失调的骨骼重塑。模型检查破骨细胞(骨吸收)和成骨细胞(骨形成)之间的关键信号。破骨细胞和成骨细胞的相互作用被建模为这些细胞群的微分方程系统,在正常情况下表现出稳定的振荡,而在骨髓瘤情况下表现出不稳定的振荡。对于未经治疗的骨髓瘤,破骨细胞增加而成骨细胞减少,随着肿瘤的生长,骨净流失。检查了靶向骨髓瘤细胞和骨髓微环境细胞对这些动力学的治疗作用。结论当前的模型可以准确反映骨髓瘤的骨病,并说明如何使用这种计算方法来研究治疗方法。审阅者本文由Ariosto Silva和Mark P. Little审阅。

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