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双膦酸盐阿仑膦酸钠对犬骨肉瘤细胞体外活力的影响。

The effect of the bisphosphonate alendronate on viability of canine osteosarcoma cells in vitro.

作者信息

Farese James P, Ashton Jenna, Milner Rowan, Ambrose Linda-Lee, Van Gilder James

机构信息

Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA.

出版信息

In Vitro Cell Dev Biol Anim. 2004 Mar-Apr;40(3-4):113-7. doi: 10.1290/1543-706x(2004)040<0113:teotba>2.0.co;2.

Abstract

The objective of this study was to determine the effect of alendronate on the viability of canine osteosarcoma cells and nonneoplastic canine cells. The sample population was composed of canine osteosarcoma tumor cells. Osteosarcoma cells and canine fibroblasts were maintained in culture under standard conditions. The MTT assay for cell viability was performed after 24, 48, and 72 h of incubation with alendronate (0.001 to 1000 microM) or no drug (control). Plates were set up so that each concentration and the control had a sample number of 8. The optical density (OD) of each well was measured at 540 nm using an enzyme-linked immunosorbent assay microplate reader. The percent viability was determined for each concentration and for each incubation time. After 24 h of incubation of POS (parent osteosarcoma) and HMPOS cells with alendronate, there was no significant difference in mean OD at any drug concentration when compared with control samples. A significant concentration- and time-dependent reduction in mean OD of osteosarcoma cells was observed after 48 and 72 h of incubation, with alendronate concentrations ranging from 10 to 1000 microM. The lowest percent cell viability observed in treated cells was 35%. Conversely, alendronate did not significantly affect mean OD in fibroblasts, and the lowest percent cell viability observed was 76%. Our data indicate that alendronate may have the potential to inhibit canine osteosarcoma tumor growth. It will be important to determine the clinical relevance of these in vitro findings. If similar findings are observed in vivo, use of alendronate may also be indicated as an adjuvant to existing chemotherapeutic protocols.

摘要

本研究的目的是确定阿仑膦酸盐对犬骨肉瘤细胞和非肿瘤性犬细胞活力的影响。样本群体由犬骨肉瘤肿瘤细胞组成。骨肉瘤细胞和犬成纤维细胞在标准条件下进行培养。在用阿仑膦酸盐(0.001至1000微摩尔)或无药物(对照)孵育24、48和72小时后,进行细胞活力的MTT测定。设置平板,使每个浓度和对照的样本数量均为8个。使用酶联免疫吸附测定微孔板读数器在540纳米处测量每个孔的光密度(OD)。确定每个浓度和每个孵育时间的活力百分比。在用阿仑膦酸盐孵育POS(亲本骨肉瘤)和HMPOS细胞24小时后,与对照样品相比,任何药物浓度下的平均OD均无显著差异。在孵育48和72小时后,观察到阿仑膦酸盐浓度范围为10至1000微摩尔时,骨肉瘤细胞的平均OD有显著的浓度和时间依赖性降低。在处理过的细胞中观察到的最低细胞活力百分比为35%。相反,阿仑膦酸盐对成纤维细胞的平均OD没有显著影响,观察到的最低细胞活力百分比为76%。我们的数据表明,阿仑膦酸盐可能具有抑制犬骨肉瘤肿瘤生长的潜力。确定这些体外研究结果的临床相关性将很重要。如果在体内观察到类似的结果,阿仑膦酸盐的使用也可能被用作现有化疗方案的辅助药物。

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