@article {7932,
	title = {Abnormal bone remodeling process is due to an imbalance in the receptor activator of nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) axis in patients with solid tumors metastatic to the skeleton},
	journal = {Acta Oncologica},
	volume = {46},
	year = {2007},
	note = {Cited By :50Export Date: 21 February 2017},
	month = {2007},
	pages = {221 - 229},
	abstract = {The role of receptor activator of nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) system, and osteopontin (OPN) was studied in patients with solid tumors metastatic to the bone in relation to the type of malignancy and the neoplastic burden to the skeleton. Levels of soluble RANKL (sRANKL), OPG and OPN were assessed in 61 patients with breast, lung and prostate cancer with newly-diagnosed metastasis to the bone, in parallel with bone resorption [C-telopeptide of type-I collagen (CTX), tartrate-resistant acid phosphatase-5b (TRACP-5b)] and bone formation markers [bone-alkaline phosphatase (bALP), osteocalcin (OC), and C-terminal propeptide of collagen type-I (CICP)]. Patients had elevated serum levels of sRANKL, OPG, OPN, TRACP-5b, and bALP, and reduced OC levels compared to controls. OPG correlated with the extent of metastatic bone burden. Patients with breast and lung cancer shared increased levels of sRANKL, OPG, and OPN whereas prostate cancer patients had elevated values of OPG and bALP only. These results suggest that patients with solid tumors metastatic to the bone have severe disruption of the sRANKL/OPG axis. Breast and lung cancer seem to exert their osteolytic action through upregulation of the sRANKL/OPG system and OPN, whereas prostate cancer seems to provoke profound elevation of OPG levels only, thus leading to increased osteoblastic activity. {\textcopyright} 2007 Taylor \& Francis.},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-33847011060\&doi=10.1080\%2f02841860600635870\&partnerID=40\&md5=f8eb210ca64f581dc2552c49dba787f7},
	author = {Mountzios, G. and Dimopoulos, M.-A. and Bamias, A. and Papadopoulos, G. and Kastritis, E. and Syrigos, K. and Pavlakis, G. and Terpos, E.}
}
