Pawlak Aleksandra, Rapak Andrzej, Zbyryt Iwona, Obmińska-Mrukowicz Bożena
Department of Biochemistry, Pharmacology and Toxicology, Faculty of Veterinary Medicine, Wrocław University of Environmental and Life Sciences, Wroclaw, Poland
Laboratory of Tumor Molecular Immunobiology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Wroclaw, Poland.
In Vivo. 2014 Sep-Oct;28(5):843-50.
BACKGROUND/AIM: Lymphoma, the most common hematopoietic cancer in dogs is sensitive to chemotherapy which is the dominant treatment method. The aim of the present study was to evaluate the concentration-dependent cytotoxicity and ability to induce apoptosis of the anti-neoplastic agents cyclophosphamide (CYC), chlorambucil (CBL), cytosine arabinoside (ARA), dexamethasone (DEX), doxorubicin (DOX), etoposide (ETO), lomustine (LOM), prednisone (PRED) and vincristine (VINK) against GL-1, CL-1, CLBL-1 and Jurkat cell lines.
To determine cell viability and level of apoptosis, three different tests were performed: Thiazolyl Blue Tetrazolium Bromide (MTT), annexin V/propidium iodide (An/PI) staining and flow cytometric DNA fragmentation.
All tested substances exhibited concentration-dependent inhibitory effects on the proliferation of the examined cell lines with a different level of apoptosis induction. VINK and DOX strongly decreased the viability of canine cell lines, whereas CYC induced the highest level of apoptosis.
Canine lymphoma (CL-1, CLBL-1) and leukemia (GL-1) cell lines are a useful tool for developing new and more effective treatment regimes for canine neoplasia.
背景/目的:淋巴瘤是犬类最常见的造血系统癌症,对作为主要治疗方法的化疗敏感。本研究的目的是评估抗肿瘤药物环磷酰胺(CYC)、苯丁酸氮芥(CBL)、阿糖胞苷(ARA)、地塞米松(DEX)、多柔比星(DOX)、依托泊苷(ETO)、洛莫司汀(LOM)、泼尼松(PRED)和长春新碱(VINK)对GL-1、CL-1、CLBL-1和Jurkat细胞系的浓度依赖性细胞毒性和诱导凋亡的能力。
为了确定细胞活力和凋亡水平,进行了三种不同的试验:噻唑蓝四氮唑溴盐(MTT)、膜联蛋白V/碘化丙啶(An/PI)染色和流式细胞术DNA片段分析。
所有受试物质均对受试细胞系的增殖表现出浓度依赖性抑制作用,并诱导不同水平的凋亡。VINK和DOX强烈降低犬类细胞系的活力,而CYC诱导的凋亡水平最高。
犬淋巴瘤(CL-1、CLBL-1)和白血病(GL-1)细胞系是开发犬肿瘤新的更有效治疗方案的有用工具。