Williams L E, Banerji N, Klausner J S, Kapur V, Kanjilal S
Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul 55108, USA.
Am J Vet Res. 2001 Sep;62(9):1354-7. doi: 10.2460/ajvr.2001.62.1354.
To establish 2 vaccine-associated feline sarcoma (VAFS) cell lines and to determine their in vitro sensitivity to the chemotherapeutic agents doxorubicin and mitoxantrone.
Tumor specimens collected from 2 cats undergoing surgery for removal of vaccine-associated sarcomas.
Tumor specimens were minced and treated with trypsin under aseptic conditions to obtain single-cell suspensions, which were then cultured in vitro in medium supplemented with 5% heat-inactivated fetal bovine serum. Growth rates and sensitivity after 24 hours of exposure to various concentrations (0.1 to 100 microg/ml) of doxorubicin and mitoxantrone were assessed for each cell line. Survival of cells was estimated 3 days after exposure to the 2 agents, and the concentration of each drug that resulted in a 50% reduction in the number of viable cells (IC50) was calculated.
Two tumor-derived cell lines (FSA and FSB) were successfully established and determined to be sensitive to doxorubicin and mitoxantrone. Under the conditions tested, the IC50 of doxorubicin were 0.6 and 1.5 microg/ml for cell lines FSB and FSA, respectively. The IC50 of mitoxantrone was 0.4 microg/ml for both cell lines.
The establishment of VAFS cell lines provides a tool for the in vitro screening of antitumor drugs. Doxorubicin and mitoxantrone were effective in decreasing the number of viable cells in the 2 cell lines tested. Both of these anthracycline antibiotics have been used to treat various neoplasias in cats, and their efficacy for adjuvant treatment of vaccine-associated sarcomas should be further evaluated.
建立2种疫苗相关猫肉瘤(VAFS)细胞系,并确定它们在体外对化疗药物阿霉素和米托蒽醌的敏感性。
从2只接受手术切除疫苗相关肉瘤的猫身上采集的肿瘤标本。
将肿瘤标本切碎,在无菌条件下用胰蛋白酶处理以获得单细胞悬液,然后将其在补充有5%热灭活胎牛血清的培养基中进行体外培养。评估每种细胞系在暴露于不同浓度(0.1至100微克/毫升)的阿霉素和米托蒽醌24小时后的生长速率和敏感性。在暴露于这2种药物3天后估计细胞存活率,并计算导致活细胞数量减少50%的每种药物的浓度(IC50)。
成功建立了2种肿瘤衍生细胞系(FSA和FSB),并确定它们对阿霉素和米托蒽醌敏感。在测试条件下,细胞系FSB和FSA的阿霉素IC50分别为0.6和1.5微克/毫升。两种细胞系的米托蒽醌IC50均为0.4微克/毫升。
VAFS细胞系的建立为体外筛选抗肿瘤药物提供了一种工具。阿霉素和米托蒽醌可有效减少所测试的2种细胞系中的活细胞数量。这两种蒽环类抗生素均已用于治疗猫的各种肿瘤,它们对疫苗相关肉瘤辅助治疗的疗效应进一步评估