Moallem S A, Dehghani N, Mehri S, Shahsavand Sh, Alibolandi M, Hadizadeh F
Pharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, I.R. Iran ; Medical Toxicology Research Center, Mashhad University of Medical Sciences, Mashhad, I.R. Iran ; Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, I.R. Iran.
Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, I.R. Iran.
Res Pharm Sci. 2015 May-Jun;10(3):214-21.
Multi drug resistance (MDR) is a serious obstacle in the management of breast cancer. Therefore, overcoming MDR using novel anticancer agents is a top priority for medicinal chemists. It was found that dihydropyridines lacking calcium antagonistic activity (e.g acridinediones) possess MDR modifier potency. In this study, the capability of four novel acridine-1,8-diones derivatives 3a-d were evaluated as MDR reversing agents. In addition, the relationship between structural properties and biological effects of synthesized compounds was discussed. In vitro cytotoxicity of acridine-1,8-diones 3a-d derivatives in combination with doxorubicin (DOX) on T47D and tomoxifen-resistant T47D (TAMR-6) breast cancer cell lines were investigated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) test. Drug resistant index (DRI), which is equal to the ratio of IC50 in drug-resistant cells over IC50 in drug-sensitive cells, was calculated for each substance. Flowcytometry experiments were also implemented to distinguish cells undergoing apoptosis from those undergoing necrosis. The results from MTT and flowcytometry experiments indicated that 1 nM 3c derivative along with DOX significantly (P<0.05) increased the DOX cytotoxicity in T47D and TAMR-6 breast cancer cell lines. Synthesized compounds 3a and 3b also at concentrations of 1 nM with DOX significantly increased the cytotoxicity of DOX on T47D and TAMR-6 breast cancer cell lines. Meanwhile, 3d derivative with DOX did not exhibit good synergistic effect on cytotoxic activity of DOX, and slightly increased DOX cytotoxicity in both cell lines. Our results proposed that 3c may be an attractive lead compound for further development as a chemotherapeutic agent for MDR breast cancer therapy in combination with routine chemotherapeutic agents such as DOX.
多药耐药性(MDR)是乳腺癌治疗中的一个严重障碍。因此,利用新型抗癌药物克服MDR是药物化学家的首要任务。已发现缺乏钙拮抗活性的二氢吡啶类化合物(如吖啶二酮)具有MDR修饰剂效力。在本研究中,评估了四种新型吖啶-1,8-二酮衍生物3a-d作为MDR逆转剂的能力。此外,还讨论了合成化合物的结构性质与生物学效应之间的关系。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)试验研究了吖啶-1,8-二酮3a-d衍生物与多柔比星(DOX)联合作用对T47D和他莫昔芬耐药的T47D(TAMR-6)乳腺癌细胞系的体外细胞毒性。计算每种物质的耐药指数(DRI),其等于耐药细胞中IC50与敏感细胞中IC50的比值。还进行了流式细胞术实验,以区分经历凋亡的细胞和经历坏死的细胞。MTT和流式细胞术实验结果表明,1 nM的3c衍生物与DOX联合使用可显著(P<0.05)提高DOX对T47D和TAMR-6乳腺癌细胞系的细胞毒性。合成化合物3a和3b在1 nM浓度下与DOX联合使用也显著提高了DOX对T47D和TAMR-6乳腺癌细胞系的细胞毒性。同时,3d衍生物与DOX联合使用对DOX的细胞毒性活性未表现出良好的协同作用,且在两种细胞系中略微增加了DOX的细胞毒性。我们的结果表明,3c可能是一种有吸引力的先导化合物,可进一步开发作为联合常规化疗药物(如DOX)治疗MDR乳腺癌的化疗药物。