Comparative analysis of Doxycycline and Ayurvedic herbs to target metastatic breast cancer: An in-silico approach.

IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL
BioMedicine-Taiwan Pub Date : 2024-06-01 eCollection Date: 2024-01-01 DOI:10.37796/2211-8039.1448
Acharya Balkrishna, Rashmi Mittal, Rohan Malik, Hariom Verma, Kuldeep Singh Mehra, Hariom Chaturvedi, Okeshwar, Swami Ishdev, Ajay Kumar, Vedpriya Arya
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Abstract

Background: Metastasis of breast cancer cells to distant sites including lungs, liver, lymph node, brain and many more have substantially affected the overall survival outcome and distant metastasis free survival rate amongst the diseased individuals. Several pre-clinical and clinical studies were carried out to determine the potency of vigorous inhibitors but they extensively deteriorated the patient's quality of life. Hence, there exists an urgent need to explore potent natural remedy to fight against metastatic breast cancer.

Methods: Ayurvedic medicinal plants documented in literature for their ability to fight against breast cancer was screened and their respective active moieties were evaluated to exert inhibitory effect against MMP9. Drug like efficacy of phytochemicals were determined using Molecular docking, MD Simulation, ADMET and MM-PBSA and were further compared with synthetic analogs i.e. Doxycycline.

Results: Out of 1000 phytochemicals, 12 exerted highest binding affinity (BA) even more than -9.0 kcal/mol that was significantly higher in comparison to Doxycycline which exhibited BA of -7.3 kcal/mol. In comparison to 37 × 30 × 37 Å, 53 × 45 × 66 Å offered best binding site and the highest BA was exhibited by Viscosalactone at LYS104, ASP185, MET338, LEU39, ASN38. During MD Simulation, Viscosalactone-MMP9 complex remained stable for 20 ns and the kinetic, electrostatic and potential energies were observed to be better than Doxycycline. Furthermore, Viscosalactone obtained from Withania somnifera justified the Lipinski's Rule of 5.

Conclusion: Viscosalactone obtained from W. somnifera may act as promising drug candidate to fight against metastatic breast cancer.

针对转移性乳腺癌的强力霉素和阿育吠陀草药的比较分析:模拟方法
背景:乳腺癌细胞向肺部、肝脏、淋巴结、脑部等远处转移严重影响了患者的总体生存率和无远处转移生存率。为了确定强效抑制剂的效力,已开展了多项临床前和临床研究,但这些研究广泛地恶化了患者的生活质量。因此,迫切需要探索有效的天然疗法来对抗转移性乳腺癌:方法:筛选了文献中记载的具有抗乳腺癌能力的阿育吠陀药用植物,并评估了它们各自的活性分子对 MMP9 的抑制作用。利用分子对接、MD 模拟、ADMET 和 MM-PBSA 确定了植物化学物质的药物功效,并进一步与合成类似物(如强力霉素)进行了比较:结果:在 1000 种植物化学物质中,12 种植物化学物质的结合亲和力(BA)最高,甚至超过了-9.0 kcal/mol,明显高于多西环素,后者的结合亲和力为-7.3 kcal/mol。与 37 × 30 × 37 Å 相比,53 × 45 × 66 Å 提供了最佳的结合位点,而且粘多糖内酯在 LYS104、ASP185、MET338、LEU39 和 ASN38 处表现出最高的 BA。在 MD 模拟过程中,Viscosalactone-MMP9 复合物在 20 ns 内保持稳定,其动能、静电能和势能均优于强力霉素。此外,从睡茄(Withania somnifera)中提取的粘多糖内酯证明了利宾斯基规则(Lipinski's Rule of 5.Conclusion)的正确性:结论:从薇甘菊中提取的粘胶内酯可作为抗转移性乳腺癌的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BioMedicine-Taiwan
BioMedicine-Taiwan MEDICINE, GENERAL & INTERNAL-
CiteScore
2.80
自引率
5.90%
发文量
21
审稿时长
24 weeks
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