Abstract
Bone homeostasis is achieved through a continuous remodelling process on the bone surface of the balanced resorption of old bone by osteoclasts and the formation of new bone by osteoblasts. Local and systemic growth factors regulate the differentiation and activity of the osteoclasts and osteoblasts (and osteocytes). Maintenance and repair of normal bone result in the release of enzymes, peptides and mineral components that have been characterised as serum and urinary biochemical markers of bone remodelling [1]. High bone turnover in cancer patients is crucial for all the steps of bone metastatic disease, from the homing of circulating cancer cells into the bone (premetastatic niche) to the complication of bone metastasis (BMT) (skeletally related events [SREs]). Therefore, elevated bone turnover marker could predict bone metastasis, risk of bone progression and risk of SREs, potentially becoming a potent prognostic predictor (Fig. 2.1). For this reason, biochemical markers of bone remodelling are potentially an ideal tool for evaluating changes in bone turnover, such as those associated with malignant bone lesions and response to treatment. Osteoclast and osteoblast activity (and probably that of cancer cells) is associated with the release of distinct biochemical markers that are amenable to non-invasive measurements of the blood or urine.
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Bertoldo, F. (2017). Markers of Bone Turnover in Bone Metastasis from Prostate Cancer. In: Bertoldo, F., Boccardo, F., Bombardieri, E., Evangelista, L., Valdagni, R. (eds) Bone Metastases from Prostate Cancer . Springer, Cham. https://doi.org/10.1007/978-3-319-42327-2_2
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