Effects of Kojic Acid-mediated Sonodynamic Therapy as a Matrix Metalloprotease-9 Inhibitor against Oral Squamous Cell Carcinoma: A Bioinformatics Screening and In Vitro Analysis.

Maryam Pourhajibagher, Mojgan Alaeddini, Shahroo Etemad-Moghadam, Steven Parker, Abbas Bahador
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Abstract

Background: Oral squamous cell carcinoma (OSCC) is a type of cancer that is responsible for a significant amount of morbidity and mortality worldwide. Researchers are searching for promising therapeutic methods to manage this cancer. In this study, an in silico approach was used to evaluate the activity of sonodynamic therapy (SDT) based on the use of Kojic acid as a sonosensitizer to inhibit matrix metalloprotease-9 (MMP-9) in OSCC.

Materials and methods: The three-dimensional structure of MMP-9 was predicted and validated by computational approaches. The possible functional role of MMP-9 was determined in terms of Gene Ontology (GO) enrichment analysis. In silico, molecular docking was then performed to evaluate the binding energies of Kojic acid with MMP-9, and ADME parameters and toxicity risks were predicted. The pharmacokinetics and drug-likeness properties of Kojic acid were assessed. Moreover, after the determination of the cytotoxicity effect of Kojic acid-mediated SDT, the change of mmp-9 gene expression was assessed on OSCC cells.

Results: The results of the study showed that Kojic acid could efficiently interact with MMP-9 protein with a strong binding affinity. Kojic acid obeyed Lipinski's rule of five without violation and exhibited drug-likeness. The cytotoxic effects of Kojic acid and ultrasound waves on the OSCC cells were dose-dependent, and the lowest expression level of the mmp-9 gene was observed in SDT.

Conclusions: Overall, Kojic acid-mediated SDT as an MMP-9 inhibitor can be a promising adjuvant treatment for OSCC. The study highlights the potential of In silico approaches to evaluate therapeutic methods for cancer treatment.

曲酸介导的声动力学疗法作为基质金属蛋白酶-9抑制剂对口腔鳞状细胞癌的作用:生物信息学筛选和体外分析
背景:口腔鳞状细胞癌(OSCC)是一种在全球范围内导致大量发病和死亡的癌症。研究人员正在寻找治疗这种癌症的有效方法。在本研究中,研究人员采用了硅学方法来评估声动力疗法(SDT)在抑制基质金属蛋白酶-9(MMP-9)方面的活性:通过计算方法预测并验证了MMP-9的三维结构。通过基因本体(Gene Ontology,GO)富集分析确定了 MMP-9 的可能功能作用。然后进行了分子对接,评估了曲酸与 MMP-9 的结合能,并预测了 ADME 参数和毒性风险。评估了曲酸的药代动力学和药物相似性。此外,在确定曲酸介导的 SDT 的细胞毒性效应后,还评估了 OSCC 细胞中 mmp-9 基因表达的变化:研究结果表明,曲酸能有效地与 MMP-9 蛋白相互作用,并具有很强的结合亲和力。曲酸符合利宾斯基五则运算法则,且不违反该法则,具有药物亲和性。曲酸和超声波对OSCC细胞的细胞毒性作用呈剂量依赖性,SDT中mmp-9基因的表达水平最低:总之,曲酸介导的SDT作为一种MMP-9抑制剂,是一种很有前景的OSCC辅助治疗方法。这项研究凸显了硅学方法在评估癌症治疗方法方面的潜力。
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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