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吲哚并[2,3-]吡咯并[3,4-]咔唑LCS1269的N-糖苷通过G2期细胞周期阻滞和CDK1活性调节发挥抗胶质母细胞瘤作用:分子对接研究、生物学研究及ADMET预测

N-Glycoside of Indolo[2,3-]pyrrolo[3,4-]carbazole LCS1269 Exerts Anti-Glioblastoma Effects by G2 Cell Cycle Arrest and CDK1 Activity Modulation: Molecular Docking Studies, Biological Investigations, and ADMET Prediction.

作者信息

Kalitin Nikolay, Koroleva Natalia, Lushnikova Anna, Babaeva Maria, Samoylenkova Nadezhda, Savchenko Ekaterina, Smirnova Galina, Borisova Yulia, Kostarev Alexander, Karamysheva Aida, Pavlova Galina

机构信息

Laboratory of Tumor Cell Genetics, N.N. Blokhin National Medical Research Center of Oncology, Kashirskoe Shosse 24, 115478 Moscow, Russia.

Laboratory of Oncogenomics, N.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.

出版信息

Pharmaceuticals (Basel). 2024 Dec 6;17(12):1642. doi: 10.3390/ph17121642.

Abstract

Indolo[2,3-]pyrrolo[3,4-]carbazole scaffold is successfully used as an efficient structural motif for the design and development of different antitumor agents. In this study, we investigated the anti-glioblastoma therapeutic potential of glycosylated indolocarbazole analog LCS1269 utilizing in vitro, in vivo, and in silico approaches. Cell viability was estimated by an MTT assay. The distribution of cell cycle phases was monitored using flow cytometry. Mitotic figures were visualized by fluorescence microscopy. Quantitative RT-PCR was used to evaluate the gene expression. The protein expression was assessed by Western blotting. Molecular docking and computational ADMET were approved for the probable protein target simulations and predicted pharmacological assessments, respectively. Our findings clearly suggest that LCS1269 displayed a significant cytotoxic effect against diverse glioblastoma cell lines and patient-derived glioblastoma cultures as well as strongly suppressed xenograft growth in nude mice. LCS1269 exhibited more potent anti-proliferative activity toward glioblastoma cell lines and patient-derived glioblastoma cultures compared to conventional drug temozolomide. We further demonstrated that LCS1269 treatment caused the severe G2 phase arrest of cell cycle in a dose-dependent manner. Mechanistically, we proposed that LCS1269 could affect the CDK1 activity both by targeting active site of this enzyme and indirectly, in particular through the modulation of the Wee1/Myt1 and FOXM1/Plk1 signaling pathways, and via p21 up-regulation. LCS1269 also showed favorable pharmacological characteristics in in silico ADME prediction in comparison with staurosporine, rebeccamycin, and becatecarin as reference drugs. Further investigations of LCS1269 as an anti-glioblastoma medicinal agent could be very promising.

摘要

吲哚并[2,3 - ]吡咯并[3,4 - ]咔唑支架已成功用作设计和开发不同抗肿瘤药物的有效结构基序。在本研究中,我们利用体外、体内和计算机模拟方法研究了糖基化吲哚咔唑类似物LCS1269对胶质母细胞瘤的治疗潜力。通过MTT法评估细胞活力。使用流式细胞术监测细胞周期阶段的分布。通过荧光显微镜观察有丝分裂图像。定量RT - PCR用于评估基因表达。通过蛋白质印迹法评估蛋白质表达。分子对接和计算ADMET分别用于可能的蛋白质靶点模拟和预测的药理学评估。我们的研究结果清楚地表明,LCS1269对多种胶质母细胞瘤细胞系和患者来源的胶质母细胞瘤培养物显示出显著的细胞毒性作用,并强烈抑制裸鼠体内异种移植瘤的生长。与传统药物替莫唑胺相比,LCS1269对胶质母细胞瘤细胞系和患者来源的胶质母细胞瘤培养物表现出更强的抗增殖活性。我们进一步证明,LCS1269处理以剂量依赖性方式导致细胞周期严重阻滞在G2期。从机制上讲,我们提出LCS1269可以通过靶向该酶的活性位点并间接影响CDK1活性,特别是通过调节Wee1/Myt1和FOXM1/Plk1信号通路以及上调p21来实现。与作为参考药物的星形孢菌素、瑞贝克霉素和贝卡替丁相比,LCS1269在计算机模拟ADME预测中也显示出良好的药理学特性。进一步研究LCS1269作为抗胶质母细胞瘤药物可能非常有前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec56/11676706/58734597672d/pharmaceuticals-17-01642-g001.jpg

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