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Osteoprotegerin in Prostate Cancer Bone Metastasis

¹ Department of Urology, University of Washington, Seattle, Washington; ² Translational Genomics Research Institute, Gaithersburg, Maryland; ³ Oncology Research Centre, University of New South Wales, Department of Clinical Medicine, Prince of Wales Hospital, Randwick, Australia; and ⁴ Puget Sound VA Health Care Systems, Seattle, Washington

Requests for reprints: Eva Corey, Department of Urology, Mail Stop 356510, University of Washington, 1959 Northeast Pacific Street, Seattle, WA, 98195. Phone: 206-543-1461; Fax: 206-543-1146; E-mail: ecorey{at}u.washington.edu.

Osteoprotegerin (OPG), a critical regulator of osteoclastogenesis, is expressed by prostate cancer cells, and OPG levels are increased in patients with prostate cancer bone metastases. The objective of this study was to investigate the effects of OPG overexpression on prostate cancer cells and prostate cancer/bone cell interactions in vitro and in vivo. OPG-transfected C4-2 cells expressed 8.0 ng OPG per mL per 10⁶ cells, whereas no OPG was detected in the media of C4-2 cells transfected with a control plasmid. OPG overexpressed by C4-2 cells protected these cells from tumor necrosis factor-related apoptosis-inducing ligand–induced apoptosis and decreased osteoclast formation. Subcutaneous OPG-C4-2 and pcDNA-C4-2 tumors exhibited similar growth and take-rate characteristics. However, when grown in bone, tumor volume was decreased in OPG-C4-2 versus pcDNA-C4-2 (P = 0.0017). OPG expressed by C4-2 cells caused increases in bone mineral density (P = 0.0074) and percentage of trabecular bone volume (P = 0.007), and decreases in numbers of osteoblasts and osteoclasts when compared with intratibial pcDNA-C4-2 tumors (P = 0.003 and P = 0.019, respectively). In summary, our data show that increased expression of OPG in C4-2 cells does not directly affect proliferation of prostate cancer cells but indirectly decreases growth of C4-2 tumors in the bone environment. Our data also show that OPG expressed by C4-2 cells inhibits bone lysis associated with C4-2 bone metastasis, which results in net increases in bone volume. We therefore hypothesize that OPG expressed in prostate cancer patient bone metastases may be at least partially responsible for the osteoblastic character of most prostate cancer bone lesions.

Key Words: prostate cancer • osteoprotegerin • bone metastases • bone remodeling • osteoblast • osteoclastogenesis

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