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松萝酸对宫颈癌靶蛋白抗癌潜力的分子见解:来自地衣的新型抗癌化合物的验证

Molecular insights of anticancer potential of usnic acid towards cervical cancer target proteins: An validation for novel anti-cancer compound from lichens.

作者信息

Murugesan Balasubramanian, Subramanian Anandhi, Bakthavachalam Subha, Rajendran Kavitha, Raju Sowndarya, Gabriel Subha

机构信息

Department of Biotechnology, Vivekanandha Arts and Science College for Women, Salem, Tamilnadu, India.

Department of Microbiology, Vivekanandha Arts and Science College for Women, Salem, Tamilnadu, India.

出版信息

J Biomol Struct Dyn. 2024 Nov;42(18):9475-9493. doi: 10.1080/07391102.2023.2252076. Epub 2023 Sep 11.

Abstract

Usnic acid is a marker compound produced from numerous lichens (symbiotic association of mycobiont and phycobiont) possessing higher bioavailability, potent and selective against cancer cells. Usnic acid is an underutilized and well-documented anti-cancer compound from lichens and its activity is not yet documented against cervical cancer. The main aim of the present research is to screen the anti-cancer potential of usnic acid against cervical cancer target proteins. The drug-likeness validation of usnic acid shows nil violations against all drug-likeness rules when compared with all three screened anti-cancer standard drugs and shows some violation in drug likeness prediction. Further, ADMET screening reveals usnic acids shows effective pharmacokinetic profiles with good bioactivity scores, essential for drug delivery and metabolism. DFT analysis of usnic acid reveals less energy gap (-0.1184), hardness (0.0592 eV), and high softness (16.8918 eV) scores against three anti-cancer drug DFT scores. Molecular docking study shows usnic acid possesses excellent binding affinity with all the nine screened cervical cancer target proteins with docking scores ranging from -6.9 to -9.1 kcal/mol. Three anti-cancer drugs showed docking scores with a range of -5.2 to -8.4 kcal/mol. Further, four top-scored complexes were taken for molecular dynamic simulation study reveal that usnic acid complexes (1KTZ-usnic acid and 2BIM-usnic acid) possess good simulation trajectories with cervical cancer target proteins than the selected anti-cancer drugs.Communicated by Ramaswamy H. Sarma.

摘要

松萝酸是一种由多种地衣(真菌共生体和藻类共生体的共生联合体)产生的标记化合物,具有较高的生物利用度,对癌细胞具有强效和选择性。松萝酸是一种未得到充分利用且有充分文献记载的地衣抗癌化合物,但其对宫颈癌的活性尚未见报道。本研究的主要目的是筛选松萝酸对宫颈癌靶蛋白的抗癌潜力。与三种筛选出的抗癌标准药物相比,松萝酸的类药性验证显示其没有违反任何类药性规则,但在类药性预测方面存在一些违规情况。此外,ADMET筛选显示松萝酸具有有效的药代动力学特征和良好的生物活性分数,这对药物递送和代谢至关重要。松萝酸的密度泛函理论(DFT)分析显示,与三种抗癌药物的DFT分数相比,其能隙(-0.1184)、硬度(0.0592 eV)较低,柔软度(16.8918 eV)较高。分子对接研究表明,松萝酸与所有九种筛选出的宫颈癌靶蛋白具有优异的结合亲和力,对接分数范围为-6.9至-9.1 kcal/mol。三种抗癌药物的对接分数范围为-5.2至-8.4 kcal/mol。此外,对四个得分最高的复合物进行分子动力学模拟研究发现,松萝酸复合物(1KTZ-松萝酸和2BIM-松萝酸)与宫颈癌靶蛋白的模拟轨迹比所选抗癌药物更好。由拉马斯瓦米·H·萨尔马传达。

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