Young D M, Fioravanti J L, Prieur D J, Ward J M
Lab Invest. 1976 Jul;35(1):30-46.
Rabbits receiving intramuscular injections of VX-2 carcinoma cells in biceps femoris muscles developed rapidly progressive neoplastic growths at 14 to 21 days associated with a significant hypercalcemia. The biologic behavior of the VX-2 carcinoma was characterized by local infiltration and metastases to regional lymph nodes and lungs. No metastases to skeletal tissues were evident. Femora from intramuscularly injected rabbits had varying degrees of osteophytosis and lysis evident roentgenographically. Histopathologic evaluation of femoral sections revealed periosteal new bone growth, cortical osteolysis, endosteal new bone growth, and in a few long term rabbits, pathologic fractures. Bone lesions were evident histologically in the vicinity of neoplastic growth (i.e., femora, tibiae) but not at distant sites (i.e., humeri and vertebrae). Mineral analyses of VX-2 carcinoma tissues and kidneys from VX-2-bearing rabbits revealed concentrations of calcium 83 and 3 times greater, respectively, than those of skeletal muscle and kidneys from controls. These findings correlated well with histochemical evidence of excessive amounts of calcium in sections of kidneys and VX-2 carcinoma tissues. Rabbits receiving intraperitoneal injections of VX-2 carcinoma cells did not develop hypercalcemia despite an extensive, progressive neoplastic burden with metastases to abdominal and thoracic viscera. Roentgenographic, histopathologic, and physiochemical analyses of selected bones from these rabbits revealed no significant alterations. These findings indicate that VX-2 carcinoma cells need to be in close proximity to skeletal tissues in order to induce hypercalcemia. The development of a significant hypercalcemia in intramuscularly injected rabbits precedes the invasion of osseous tissues by VX-2 carcinoma cells. Therefore, it appears that VX-2 carcinoma cells have the ability to alter skeletal morphology and physiochemistry through a dual humoral/cellular mechanism. The clinicopathologic characteristics of the VX-2 carcinoma in the rabbit suggest that the neoplasm is a good experimental model to study osseous-mediated hypercalcemia of malignancy.
在股二头肌接受VX - 2癌细胞肌肉注射的兔子,在14至21天出现快速进展的肿瘤生长,并伴有明显的高钙血症。VX - 2癌的生物学行为表现为局部浸润以及向区域淋巴结和肺部转移。未发现向骨骼组织转移。肌肉注射兔子的股骨在X线片上有不同程度的骨赘形成和骨质溶解。股骨切片的组织病理学评估显示有骨膜新生骨形成、皮质骨溶解、骨内膜新生骨形成,并且在一些长期存活的兔子中出现病理性骨折。在肿瘤生长附近的骨骼(即股骨、胫骨)组织学上可见骨病变,但在远处部位(即肱骨和椎骨)未见。对VX - 2癌组织和荷VX - 2兔的肾脏进行矿物质分析发现,钙浓度分别比对照组骨骼肌和肾脏高83倍和3倍。这些发现与肾脏和VX - 2癌组织切片中过量钙的组织化学证据密切相关。接受VX - 2癌细胞腹腔注射的兔子尽管有广泛进展的肿瘤负荷并转移至腹部和胸部脏器,但未发生高钙血症。对这些兔子的选定骨骼进行X线、组织病理学和物理化学分析未发现明显改变。这些发现表明,VX - 2癌细胞需要与骨骼组织紧密相邻才能诱导高钙血症。肌肉注射兔子中明显高钙血症的发生先于VX - 2癌细胞对骨组织的侵袭。因此,似乎VX - 2癌细胞有能力通过体液/细胞双重机制改变骨骼形态和物理化学性质。兔子VX - 2癌的临床病理特征表明,该肿瘤是研究骨介导的恶性肿瘤高钙血症的良好实验模型。