Aspergillus Carneus metabolite Averufanin induced cell cycle arrest and apoptotic cell death on cancer cell lines via inducing DNA damage

• Published in: Scientific reports 2023-04, Vol.13 (1), p.6460-6460, Article 6460
• Main Authors: Demirel, Deren, Ozkaya, Ferhat Can, Ebrahim, Weaam, Sokullu, Emel, Sahin, Irem Durmaz
• Format: Article
• Language: English
• Subjects: 631/154; 631/337; 631/67; Annexin V; Apoptosis; Aspergillus; Breast cancer; Breast Neoplasms - metabolism; Cancer therapies; Caspase-3; Cell Cycle; Cell Cycle Checkpoints; Cell death; Cell Line; Cell Line, Tumor; Chemotherapy; Cytotoxicity; Deoxyribonucleic acid; DNA; DNA Damage; Female; Glioblastoma; Humanities and Social Sciences; Humans; Immunotherapy; Metabolites; Molecular modelling; Mortality; multidisciplinary; Ovarian cancer; Science; Science (multidisciplinary); Side effects; Tumor cell lines; γ Radiation
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-30775-w

Cancer is one of the leading causes of death worldwide, accounting for nearly 10 million deaths in 2020. Current treatment methods include hormone therapy, γ-radiation, immunotherapy, and chemotherapy. Although chemotherapy is the most effective treatment, there are major obstacles posed by resistance mechanisms of cancer cells and side-effects of the drugs, thus the search for novel anti-cancer compounds, especially from natural sources, is crucial for cancer pharmaceutics research. One natural source worthy of investigation is fungal species. In this study, the cytotoxicity of 5 metabolic compounds isolated from filamentous fungus Aspergillus Carneus. Arugosin C, Averufin, Averufanin, Nidurifin and Versicolorin C were analyzed using NCI-SRB assay on 10 different cell lines of breast cancer, ovarian cancer, glioblastoma and non-tumorigenic cell lines. Averufanin showed highest cytotoxicity with lowest IC 50 concentrations especially on breast cancer cells. Therefore, Averufanin was further investigated to enlighten cell death and molecular mechanisms of action involved. Cell cycle analysis showed increase in SubG1 phase suggesting apoptosis induction which was further confirmed by Annexin V and Caspase 3/7 Assays. H2A.X staining revealed accumulation of DNA damage in cells treated with Averufanin and finally western blot analysis validated DNA damage response and downstream effects of Averufanin treatment in various signaling pathways. Consequently, this study shows that Averufanin compound induces cell cycle arrest and cell death via apoptosis through causing DNA damage and can be contemplated and further explored as a new therapeutic strategy in breast cancer.