Department of Radiation Sciences and Oncology, Umeå University, SE-90187, Umeå, Sweden.
Anticancer Res. 2012 Jul;32(7):2407-13.
The malignant brain tumour glioblastoma is a devastating disease that remains a therapeutic challenge.
Effects of combinations of the US Food and Drug Administation (FDA) approved proteasome inhibitor bortezomib and the histone deacetylase (HDAC) inhibitors vorinostat, valproic acid and sodium phenylbutyrate were studied on primary glioblastoma stem cell lines and conventional glioblastoma cell lines. Cell survival, proliferation and death were analyzed by fluorometric microculture cytotoxicity assay (FMCA), propidium iodide labeling and flow cytometry, and cell cloning through limiting dilution and live-cell bright-field microscopy.
Bortezomib and the HDAC inhibitors showed synergistic cell killing at clinically relevant drug concentrations, while the conventional cell lines cultured in serum-containing medium were relatively resistant to the same treatments.
These findings of synergistic glioblastoma stem cell killing by bortezomib and three different FDA-approved HDAC inhibitors confirm and expand previous observations on co-operative effects between these classes of drugs.
恶性脑肿瘤胶质母细胞瘤是一种毁灭性疾病,仍然是治疗的挑战。
研究了美国食品和药物管理局 (FDA) 批准的蛋白酶体抑制剂硼替佐米和组蛋白去乙酰化酶 (HDAC) 抑制剂伏立诺他、丙戊酸和苯丁酸钠联合使用对原发性脑胶质瘤干细胞系和常规脑胶质瘤细胞系的影响。通过荧光微培养细胞毒性测定 (FMCA)、碘化丙啶标记和流式细胞术以及通过有限稀释和活细胞明场显微镜进行细胞克隆来分析细胞存活、增殖和死亡。
硼替佐米和 HDAC 抑制剂在临床相关药物浓度下表现出协同细胞杀伤作用,而在含血清培养基中培养的常规细胞系对相同处理相对耐药。
这些硼替佐米和三种不同的 FDA 批准的 HDAC 抑制剂协同杀伤脑胶质瘤干细胞的发现证实并扩展了这两类药物之间协同作用的先前观察结果。