Abstract
Maintenance of a healthy skeleton requires a stable relationship between osteoblast and osteoclast activity. When cancer cells spread to bone, they interact with the bone cells to express bone-like proteins and participate with bone cells in inducing osteoclasts and osteoblasts, thereby bringing about a metabolic imbalance between osteoblasts and osteoclasts. This imbalance may favor osteosclerotic/osteoblastic processes, as in prostate cancer (PCa) or osteosarcoma, or activate osteolytic processes, as in breast cancer and myeloma. The ability of cancer cells to undergo phenotypic changes that allow them to form bone is termed “osteomimicry” and permits cancer cells to home, adhere, and migrate to bone, to invade bone space, and then to utilize the rich bone microenvironment to proliferate and survive because of the abundance of growth factors (GFs) and extracellular matrix molecules (ECMs) found in the bone niche (see Chapter 1).
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Abbreviations
- PCa:
-
prostate cancer
- PSA:
-
prostate-specific antigen
- OC:
-
osteocalcin
- BSP:
-
bone sialoprotein
- RANKL:
-
receptor activator of NFκB ligand
- HS:
-
heparan sulfate
- HSPG:
-
heparan sulfate proteoglycan
- HPSE:
-
heparanase
- ROS:
-
reactive oxygen species
- β2-M:
-
β2-microglobulin
- PKA:
-
protein kinase A
- EMT:
-
epithelial-to-mesenchymal transition
- NED:
-
neuroendocrine differentiation
- GFs:
-
growth factors
- ECMs:
-
extracellular matrices
- CREB:
-
cyclic AMP-responsive element binding protein
- FGF:
-
fibroblast growth factor
- VEGF:
-
vascular endothelial growth factor
- TGF-β:
-
transforming growth factor β
- BMPs:
-
bone morphogenetic proteins
- PIN:
-
prostate intraepithelial neoplasia
- FAK:
-
focal adhesion kinase
- MMPs:
-
matrix metalloproteinases
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Chung, L.W., Zhau, H.E., Petros, J.A., Farach-Carson, M.C. (2010). Prostate Cancer Bone Colonization: Osteomimicry in the Bone Niche. In: Bone and Cancer. Topics in Bone Biology, vol 5. Springer, London. https://doi.org/10.1007/978-1-84882-019-7_10
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