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土壤来源的枯草芽孢杆菌代谢产物对乳腺癌的特性研究:体外和计算机模拟研究

Characterization of soil-derived Bacillus subtilis metabolites against breast cancer: In vitro and in silico studies.

作者信息

Hashmi Ayesha Irfan, Iqtedar Mehwish, Saeed Hamid, Ahmed Nadeem, Abdullah Roheena, Kaleem Afshan, Abbasi Muhammad Athar

机构信息

Department of Biotechnology, Lahore College for Women University, Lahore, Pakistan.

University College of Pharmacy, University of the Punjab, Allama Iqbal Campus, Lahore, 54000, Pakistan.

出版信息

Saudi Pharm J. 2025 Apr 17;33(1-2):3. doi: 10.1007/s44446-025-00006-6.

Abstract

Breast cancer remains one of the most challenging and widespread cancers among women globally that warrants further investigations for novel agents to minimize side effects and disease recurrence. In this study, a soil bacterium was isolated and 16S rRNA nucleotide sequence homology and resultant phylogenetic tree analysis confirmed Bacillus subtills (CP020102.1). The crude extract of bacterial strain showed cytotoxicity (cell viability 63.1%) against human breast cancer cell line MCF-7 through MTT assay followed by further analysis through preparative HPLC showing 29 active fractions. Among all fractions, fraction 16 demonstrated cytotoxic potential as low as 54.03%. The spectral data of LC-MS, NMR and FTIR identified the bioactive compound as isatin based bacterial metabolite (Z)-N'-(1-hexyl-2-oxoindolin-3-ylidene)-4-methylbenzenesulfonohydrazide. This bioactive compound upon in silico docking analysis with HER2 showed a binding energy of -8.8 kcal/mol. ADMET calculations determined the pharmacokinetic behavior of the compound revealing acceptable distribution and absorption profiles. The drug-likeness of the compound was confirmed based on the Lipinski rule with zero violations. Molecular dynamic simulation (MDS) was also performed for 100 ns and a stable RMSF plot was observed. The results strongly propose that the identified compound has immense potential to be considered a drug candidate to develop further against human breast cancer.

摘要

乳腺癌仍然是全球女性中最具挑战性和最为普遍的癌症之一,因此有必要进一步研究新型药物,以尽量减少副作用和疾病复发。在本研究中,分离出一种土壤细菌,通过16S rRNA核苷酸序列同源性分析和由此产生的系统发育树分析,确定该细菌为枯草芽孢杆菌(CP020102.1)。通过MTT法检测,该细菌菌株的粗提物对人乳腺癌细胞系MCF-7显示出细胞毒性(细胞活力为63.1%),随后通过制备型高效液相色谱进一步分析,得到29个活性组分。在所有组分中,组分16表现出低至54.03%的细胞毒性潜力。液相色谱-质谱联用(LC-MS)、核磁共振(NMR)和傅里叶变换红外光谱(FTIR)的光谱数据确定该生物活性化合物为基于异吲哚酮的细菌代谢产物(Z)-N'-(1-己基-2-氧代吲哚啉-3-基亚基)-4-甲基苯磺酰肼。该生物活性化合物与HER2进行计算机对接分析时,显示出-8.8 kcal/mol的结合能。ADMET计算确定了该化合物的药代动力学行为,显示出可接受的分布和吸收情况。根据Lipinski规则,该化合物的类药性得到确认,没有违反任何规则。还进行了100纳秒的分子动力学模拟(MDS),观察到一个稳定的均方根波动(RMSF)图。结果有力地表明,所鉴定的化合物具有巨大的潜力,有望被进一步开发成为抗人类乳腺癌的候选药物。

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