8-(2-甲基苯基)- 9h -benzo[f]indeno[2,1-c]quinolin-9-one (C-5635020)作为乳腺癌治疗的新型选择性TGFβ RII激酶抑制剂的鉴定

IF 2.5 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochemical and biophysical research communications Pub Date : 2025-02-01 Epub Date: 2025-01-02 DOI:10.1016/j.bbrc.2024.151225
Mesfer Al Shahrani, Mohammad Abohassan, Mohammad Alshahrani, Reem M Gahtani, Prasanna Rajagopalan
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引用次数: 0

摘要

目的与意义:转化生长因子-β (TGF-β)在乳腺发育过程中通过调节组织组成发挥关键作用。TGFβ II型受体(TGFβ RII)与乳腺癌有关,是一个有价值的治疗靶点。由于许多现有的TGFβ i /TGFβ RII抑制剂的脱靶副作用,有必要采用更有针对性的方法来发现药物。本研究采用计算建模和分子动力学模拟来筛选ChemBridge小分子文库对抗TGFβ RII。方法:采用高通量虚拟筛选、分子动力学模拟、结合自由能计算等方法,鉴定TGF-β RII靶向抑制剂。MDA-MB 231和MCF-7乳腺癌细胞用于抗增殖、反内皮迁移和流式细胞术检测,以进行体外验证。结果:我们鉴定出8-(2-甲基苯基)- 9h -苯并[f]indeno[2,1-c]喹啉-9-one (C-5635020)是一种有效的选择性抑制剂。蛋白质配体模型分析显示,与标准药物staurosporine相比,C-5635020靶向TGFβ RII的激酶结构域,具有更好的结合亲和力。计算结果表明,C-5635020选择性结合并抑制TGFβ RII活性,从而控制乳腺癌细胞增殖。体外实验证实了这些预测,其中C-5635020抑制MDAMB-231和MCF-7细胞中的TGFβ RII和p-Smad 2/3阳性群体。该化合物剂量依赖性地抑制两种乳腺癌细胞系的细胞增殖、跨内皮细胞迁移和增加细胞凋亡。结论:C-5635020具有较强的结合亲和力、稳定性和良好的热力学特性,具有良好的体外疗效,具有作为乳腺癌临床前和临床开发先导化合物的潜力。
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Identification of 8-(2-methyl phenyl)-9H-benzo[f]indeno[2,1-c]quinolin-9-one (C-5635020) as a novel and selective TGFβ RII kinase inhibitor for breast cancer therapy.

Objective and significance: Transforming growth factor-beta (TGF-β) plays a pivotal role in breast development by modulating tissue composition during the developmental phase. The TGFβ type II receptor (TGFβ RII) is implicated in breast cancer and represents a valuable therapeutic target. Due to the off-target side effects of many existing TGFβI/TGFβ RII inhibitors, a more targeted approach to drug discovery is necessary. This study used computational modeling and molecular dynamics simulations to screen the ChemBridge small molecule library against TGFβ RII.

Methods: This study employed high-throughput virtual screening, molecular dynamics simulations, and binding free energy calculations to identify potential inhibitors targeting TGF-β RII. MDA-MB 231 and MCF-7 breast cancer cells were used in anti-proliferative, tans-endothelial migration, and flow cytometric assays for in vitro validations.

Results: We identified 8-(2-methylphenyl)-9H-benzo[f]indeno[2,1-c]quinolin-9-one (C-5635020) as a potent and selective inhibitor. Protein-ligand modeling analysis revealed that C-5635020 targets the kinase domain of TGFβ RII with superior binding affinities compared to the standard drug, staurosporine. Computational results suggest that C-5635020 selectively binds and inhibits TGFβ RII activity, thereby controlling cell proliferation in breast cancer. In vitro, experiments corroborated these predictions, where C-5635020 inhibited TGFβ RII and p-Smad 2/3 positive population in MDAMB-231 and MCF-7 cells. The compound dose-dependently inhibited cell proliferation, trans-endothelial migration, and increased apoptosis in both breast cancer cell lines.

Conclusion: The strong binding affinity, stability, and favorable thermodynamics of C-5635020 with established in vitro efficacy highlight its potential as a lead compound for further preclinical and clinical developments for breast cancer treatment.

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来源期刊
Biochemical and biophysical research communications
Biochemical and biophysical research communications 生物-生化与分子生物学
CiteScore
6.10
自引率
0.00%
发文量
1400
审稿时长
14 days
期刊介绍: Biochemical and Biophysical Research Communications is the premier international journal devoted to the very rapid dissemination of timely and significant experimental results in diverse fields of biological research. The development of the "Breakthroughs and Views" section brings the minireview format to the journal, and issues often contain collections of special interest manuscripts. BBRC is published weekly (52 issues/year).Research Areas now include: Biochemistry; biophysics; cell biology; developmental biology; immunology ; molecular biology; neurobiology; plant biology and proteomics
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