Capparelli C, Kostenuik P J, Morony S, Starnes C, Weimann B, Van G, Scully S, Qi M, Lacey D L, Dunstan C R
Department of Pathology, Amgen Inc., Thousand Oaks, California 91320-1789, USA.
Cancer Res. 2000 Feb 15;60(4):783-7.
Osteoprotegerin (OPG), a novel, secreted tumor necrosis factor receptor family member that inhibits osteoclast formation and activity was examined for its activity in a syngeneic tumor model of humoral hypercalcemia of malignancy. Normal mice bearing Colon-26 tumors develop increases in both parathyroid hormone-related protein (PTHrP) expression and plasma PTHrP, marked hypercalcemia, and increased bone resorption. OPG, given either at the onset of hypercalcemia or after it had occurred, blocked tumor-induced increases in bone resorption and hypercalcemia and rapidly normalized blood ionized calcium. In tumor-bearing mice, OPG treatments reduced osteoclast activity from approximately 2-fold above normal into the subphysiological range but had no effects on tumor size, tumor-induced cachexia, or PTHrP levels. The potent effects of OPG in this humoral hypercalcemia of malignancy model suggest a potential therapeutic role for OPG in the prevention and treatment of this disorder.
骨保护素(OPG)是一种新发现的、分泌型肿瘤坏死因子受体家族成员,可抑制破骨细胞的形成和活性。我们在恶性肿瘤体液性高钙血症的同基因肿瘤模型中检测了其活性。携带结肠26肿瘤的正常小鼠甲状旁腺激素相关蛋白(PTHrP)表达和血浆PTHrP均升高,出现明显的高钙血症,骨吸收增加。在高钙血症发作时或发作后给予OPG,可阻断肿瘤诱导的骨吸收增加和高钙血症,并迅速使血液离子钙恢复正常。在荷瘤小鼠中,OPG治疗可将破骨细胞活性从高于正常水平约2倍降低至亚生理范围,但对肿瘤大小、肿瘤诱导的恶病质或PTHrP水平无影响。OPG在该恶性肿瘤体液性高钙血症模型中的强效作用表明,OPG在预防和治疗该疾病方面具有潜在的治疗作用。