Ashton Jenna A, Farese James P, Milner Rowan J, Lee-Ambrose Linda M, van Gilder James M
Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610-0126, USA.
Am J Vet Res. 2005 May;66(5):885-91. doi: 10.2460/ajvr.2005.66.885.
To determine the effect of pamidronate disodium on the in vitro viability of osteosarcoma cells and non-neoplastic cells from dogs.
3 osteosarcoma and 1 fibroblast cell lines derived from dogs.
Cell counts and cell viability assays were performed in cultures of osteosarcoma cells (POS, HMPOS, and COS31 cell lines) and fibroblasts after 24, 48, and 72 hours of incubation with pamidronate at concentrations of 0.001 to 1000 microM or with no drug (control treatment). Percentage viability was determined in cell samples for each concentration of pamidronate and each incubation time. A DNA fragmentation analysis was performed to assess bisphosphonate-induced apoptosis.
Osteosarcoma cell viability decreased significantly in a concentration- and time-dependent manner at pamidronate concentrations ranging from 100 to 1000 microM, most consistently after 48 and 72 hours' exposure. In treated osteosarcoma cells, the lowest percentage cell viability was 34% (detected after 72 hours' exposure to 1000 microM pamidronate). Conversely, 72 hours' exposure to 1000 microM pamidronate did not significantly reduce fibroblast viability (the lowest percentage viability was 76%). After 72 hours of exposure, pamidronate did not cause DNA fragmentation in POS or HMPOS cells.
Results indicate that pamidronate may have the potential to inhibit osteosarcoma growth in dogs, possibly through a nonapoptotic mechanism. The clinical relevance of these in vitro findings remains to be determined, but administration of pamidronate may potentially be indicated as an adjuvant treatment in chemotherapeutic protocols used in dogs.
确定帕米膦酸二钠对犬骨肉瘤细胞和非肿瘤细胞体外活力的影响。
源自犬的3种骨肉瘤细胞系和1种成纤维细胞系。
在骨肉瘤细胞(POS、HMPOS和COS31细胞系)和成纤维细胞培养物中,用浓度为0.001至1000微摩尔的帕米膦酸或无药物(对照处理)孵育24、48和72小时后,进行细胞计数和细胞活力测定。测定每种帕米膦酸浓度和每种孵育时间下细胞样本的活力百分比。进行DNA片段化分析以评估双膦酸盐诱导的细胞凋亡。
在帕米膦酸浓度为100至1000微摩尔时,骨肉瘤细胞活力以浓度和时间依赖性方式显著降低,在暴露48和72小时后最为一致。在经处理的骨肉瘤细胞中,最低的细胞活力百分比为34%(在暴露于1000微摩尔帕米膦酸72小时后检测到)。相反,暴露于1000微摩尔帕米膦酸72小时并未显著降低成纤维细胞活力(最低活力百分比为76%)。暴露72小时后,帕米膦酸未在POS或HMPOS细胞中引起DNA片段化。
结果表明,帕米膦酸可能有潜力抑制犬骨肉瘤生长,可能通过非凋亡机制。这些体外研究结果的临床意义仍有待确定,但帕米膦酸给药可能有潜力作为犬化疗方案中的辅助治疗。