AI Article Synopsis

  • Oral squamous cell carcinoma (OSCC) is a serious cancer globally, prompting research into new treatments, specifically using sonodynamic therapy (SDT) with Kojic acid to inhibit the MMP-9 protein, linked to cancer progression.* ! -
  • The study involved predicting MMP-9's structure and performing molecular docking to assess how Kojic acid binds to it, confirming drug-like qualities and evaluating its effects on OSCC cells.* ! -
  • Results indicated that Kojic acid strongly binds to MMP-9, is non-toxic, and effectively reduces mmp-9 gene expression in OSCC cells through a dose-dependent mechanism, suggesting this approach could serve as a valuable treatment option.* !

Article 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 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. , 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 approaches to evaluate therapeutic methods for cancer treatment.

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http://dx.doi.org/10.2174/0115701638266082231124055825DOI Listing

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