Santoshi Seneha, Manchukonda Naresh Kumar, Suri Charu, Sharma Manya, Sridhar Balasubramanian, Joseph Silja, Lopus Manu, Kantevari Srinivas, Baitharu Iswar, Naik Pradeep Kumar
Department of Biotechnology and Bioinformatics, Jaypee University of Information Technology, Waknaghat, Distt. Solan, 173 234, Himachal Pradesh, India.
J Comput Aided Mol Des. 2015 Mar;29(3):249-70. doi: 10.1007/s10822-014-9820-5. Epub 2014 Dec 7.
We have strategically designed a series of noscapine derivatives by inserting biaryl pharmacophore (a major structural constituent of many of the microtubule-targeting natural anticancer compounds) onto the scaffold structure of noscapine. Molecular interaction of these derivatives with α,β-tubulin heterodimer was investigated by molecular docking, molecular dynamics simulation, and binding free energy calculation. The predictive binding affinity indicates that the newly designed noscapinoids bind to tubulin with a greater affinity. The predictive binding free energy (ΔG(bind, pred)) of these derivatives (ranging from -5.568 to -5.970 kcal/mol) based on linear interaction energy (LIE) method with a surface generalized Born (SGB) continuum solvation model showed improved binding affinity with tubulin compared to the lead compound, natural α-noscapine (-5.505 kcal/mol). Guided by the computational findings, these new biaryl type α-noscapine congeners were synthesized from 9-bromo-α-noscapine using optimized Suzuki reaction conditions for further experimental evaluation. The derivatives showed improved inhibition of the proliferation of human breast cancer cells (MCF-7), human cervical cancer cells (HeLa) and human lung adenocarcinoma cells (A549), compared to natural noscapine. The cell cycle analysis in MCF-7 further revealed that these compounds alter the cell cycle profile and cause mitotic arrest at G2/M phase more strongly than noscapine. Tubulin binding assay revealed higher binding affinity to tubulin, as suggested by dissociation constant (Kd) of 126 ± 5.0 µM for 5a, 107 ± 5.0 µM for 5c, 70 ± 4.0 µM for 5d, and 68 ± 6.0 µM for 5e compared to noscapine (Kd of 152 ± 1.0 µM). In fact, the experimentally determined value of ΔG(bind, expt) (calculated from the Kd value) are consistent with the predicted value of ΔG(bind, pred) calculated based on LIE-SGB. Based on these results, one of the derivative 5e of this series was used for further toxicological evaluation. Treatment of mice with a daily dose of 300 mg/kg and a single dose of 600 mg/kg indicates that the compound does not induce detectable pathological abnormalities in normal tissues. Also there were no significant differences in hematological parameters between the treated and untreated groups. Hence, the newly designed noscapinoid, 5e is an orally bioavailable, safe and effective anticancer agent with a potential for the treatment of cancer and might be a candidate for clinical evaluation.
我们通过将联芳基药效团(许多靶向微管的天然抗癌化合物的主要结构成分)插入到那可丁的支架结构上,战略性地设计了一系列那可丁衍生物。通过分子对接、分子动力学模拟和结合自由能计算,研究了这些衍生物与α,β-微管蛋白异二聚体的分子相互作用。预测的结合亲和力表明,新设计的那可丁类化合物与微管蛋白的结合亲和力更高。基于线性相互作用能(LIE)方法和表面广义玻恩(SGB)连续介质溶剂化模型,这些衍生物(范围为-5.568至-5.970 kcal/mol)的预测结合自由能(ΔG(bind, pred))显示,与先导化合物天然α-那可丁(-5.505 kcal/mol)相比,与微管蛋白的结合亲和力有所提高。在计算结果的指导下,使用优化的铃木反应条件,由9-溴-α-那可丁合成了这些新的联芳基型α-那可丁同系物,以进行进一步的实验评估。与天然那可丁相比,这些衍生物对人乳腺癌细胞(MCF-7)、人宫颈癌细胞(HeLa)和人肺腺癌细胞(A549)的增殖抑制作用有所增强。MCF-7细胞周期分析进一步表明,这些化合物改变了细胞周期分布,并且比那可丁更强烈地导致有丝分裂停滞在G2/M期。微管蛋白结合试验显示,与那可丁(解离常数Kd为152±1.0 µM)相比,5a的解离常数Kd为126±5.0 µM,5c为107±5.0 µM,5d为70±4.0 µM,5e为68±6.0 µM,表明对微管蛋白具有更高的结合亲和力。事实上,实验测定的ΔG(bind, expt)值(由Kd值计算得出)与基于LIE-SGB计算的ΔG(bind, pred)预测值一致。基于这些结果,该系列中的一种衍生物5e被用于进一步毒理学评估。以每日剂量300 mg/kg和单次剂量600 mg/kg对小鼠进行治疗表明,该化合物在正常组织中未诱导可检测到的病理异常。治疗组和未治疗组的血液学参数也没有显著差异。因此,新设计的那可丁类化合物5e是一种口服生物可利用、安全有效的抗癌剂,具有治疗癌症的潜力,可能是临床评估的候选药物。