Waki Y, Miyamoto K, Kasugai S, Ohya K
Research Laboratory for Development of Medicine, Faculty of Pharmaceutical Sciences, Hokuriku University, Kanazawa.
Jpn J Cancer Res. 1995 May;86(5):470-6. doi: 10.1111/j.1349-7006.1995.tb03080.x.
Walker carcinoma 256 (W256) was reported to induce hypercalcemia dependent on bone metastasis and/or parathyroid hormone-related protein (PTHrP) in the rat, providing a model of the humoral hypercalcemia of malignancy. In this study, after the subcutaneous inoculation of cells of the W256/S line, which is maintained in this laboratory, into young female Wistar Imamichi rats (6 weeks old), serum calcium and phosphorus levels changed only within the control range, whereas serum alkaline phosphatase activity and urinary calcium level significantly increased and urinary phosphorus decreased during the tumor growth, resulting in hypercalciuria and hypophosphaturia. W256/S did not express PTHrP-mRNA, whereas LLC-W256 cells did express it. Serum PTHrP level was not changed in W256/S-bearing rats. Osteoporosis-like changes, bone weight loss, low contents of bone calcium and phosphorus, and a decrease in the bone mineral density (BMD), were observed in the femur 14 days after the tumor inoculation. There was a pronounced decrease in the serum 17 beta-estradiol level during the tumor growth. The reduction of BMD of femurs in W256/S-bearing rats was significantly inhibited by treatment with salmon calcitonin or 17 beta-estradiol. On the basis of these results, W256/S carcinoma-bearing rats seem to be a useful model for osteoporosis of hypoovarianism.
据报道,Walker癌256(W256)可在大鼠体内诱发依赖骨转移和/或甲状旁腺激素相关蛋白(PTHrP)的高钙血症,为恶性肿瘤体液性高钙血症提供了一个模型。在本研究中,将本实验室保存的W256/S系细胞皮下接种到年轻雌性Wistar Imamichi大鼠(6周龄)体内后,血清钙和磷水平仅在对照范围内变化,而在肿瘤生长过程中血清碱性磷酸酶活性和尿钙水平显著升高,尿磷降低,导致高钙尿症和低磷尿症。W256/S不表达PTHrP-mRNA,而LLC-W256细胞表达。荷W256/S大鼠的血清PTHrP水平未发生变化。在接种肿瘤14天后,在股骨中观察到骨质疏松样改变、骨重量减轻、骨钙和磷含量降低以及骨矿物质密度(BMD)下降。在肿瘤生长过程中,血清17β-雌二醇水平显著降低。用鲑鱼降钙素或17β-雌二醇治疗可显著抑制荷W256/S大鼠股骨BMD的降低。基于这些结果,荷W256/S癌大鼠似乎是卵巢功能减退性骨质疏松症的一个有用模型。