Falakh, Muhammad F. and Zuhri, Ummu Mastna and Untari, Febriana and Murniasih, Tutik and Rachman, Fauzy and Setiawan, R. and Wibowo, Joko Tri and Hertiani, Triana (2025) Metabolomics-Guided Discovery of Anticancer Metabolites from Marine SpongeAssociated Bacillus safensis: In Vitro and In Silico Evaluation. Tropical Journal of Natural Product Research, 9 (8). 3992 - 4003. ISSN 26160684
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Abstract
Marine-derived bacteria are valuable sources of novel anticancer agents, particularly those associated with sponges in tropical ecosystems. This study aimed to investigate the cytotoxic and metabolomic profile of Bacillus safensis P.039.5, isolated from marine sponge Petrosia nigricans collected near Pari Island, Indonesia. Cytotoxic screening against MCF-7 breast cancer cells revealed significant inhibition, with an IC50 value of 186.63 μg/mL and a high selectivity index compared to doxorubicin. Metabolite profiling using Liquid Chromatography-High Resolution Mass Spectrometry (LC-HRMS/MS) identified 28 putative compounds, dominated by peptides and alkaloids. Among these, militarinone A, maculosin, and verpacamide A showed the strongest predicted binding affinities in molecular docking studies against five breast cancer-related targets: ER-α, HER2, EGFR, CDK2, and topoisomerase IIα. Militarinone A exhibited the highest binding affinity (-11.11 kcal/mol), exceeding native ligands and reference drugs. To our knowledge, this is the first report of militarinone A detection in B. safensis P.039.5, demonstrating the utility of a metabolomics-guided approach to prioritize bioactive compounds from underexplored marine bacteria. These findings highlight the pharmacological potential of B. safensis as a sustainable source of multi-target anticancer leads. © 2025 Falakh et al.
| Item Type: | Article |
|---|---|
| Additional Information: | Cited by: 0; All Open Access; Gold Open Access; Green Accepted Open Access; Green Open Access |
| Uncontrolled Keywords: | 1 (2 morpholinophenyl)dihydro 1h pyrrole 2,5 dione; 1 aminocyclopropanecarboxylic acid; 1 deoxynojirimycin; 1,3 dimethylbutylamine; 2 amino 1,3,4 octadecanetriol; 4 hydroxyprolyl 4 hydroxyproline; 4 methyleneglutamine; 6 hydroxypseudooxynicotine; adipic acid; alkaloid; amino acid; antineoplastic agent; Bacillus safensis extract; bacterial extract; betaine; bis(2 ethylhexyl) benzene 1,2 dicarboxylate; cis cyclooctene; cyclin dependent kinase 2; cyclo(leucylprolyl); Dasychalina fragilis extract; dihydrothymine; doxorubicin; drug metabolite; epidermal growth factor receptor; epidermal growth factor receptor 2; erucamide; estrogen receptor; estrogen receptor alpha; fadraciclib; glycylprolylhydroxyproline; hexylamine; indospicine; lapatinib; maculosin; methylproline; militarinone A; n methylproline; natural product; np 013736; peptide; Petrosia nigricans extract; phenylalanine; prolylglutamic acid; pyridoxamine; RNA 16S; topoisomerase II alpha; unclassified drug; verpacamide; verpacamide A; Article; Bacillus amyloliquefaciens; Bacillus pumilus; Bacillus safensis; bacterium isolation; binding affinity; binding site; biotransformation; bootstrapping; cell proliferation; cell viability; chemical phenomena; chromatography by mobile phase; controlled study; crystal structure; cytotoxicity; DNA extraction; electrospray mass spectrometry; evolutionary adaptation; fermentation; fragmentation pattern; fragmentation reaction; gene sequence; Hep-G2 cell line; horizontal gene transfer; human; human cancer cell; human cell; hydrogen bond; hydrolysis; hydrophilic interaction; IC50; in vitro study; incubation time; Levenes test; ligand binding; ligand protein interaction; liquid chromatography-mass spectrometry; marine sponge associated Bacillus safensis; mass spectrometry; MCF-7 cell line; metabolomics; microbial community; minimum peak intensity threshold; molecular docking; MTT assay; neighbor joining method; nonhuman; nucleotide recognition; nucleotide sequence; Petrosia nigricans; phylogenetic tree; protein purification; replication study; selectivity index; sequence analysis; Shapiro Wilk test; SK-LU-1 cell line; ultra performance liquid chromatography; validation study; Vero cell line |
| Subjects: | R Medicine > RM Therapeutics. Pharmacology R Medicine > RS Pharmacy and materia medica |
| Divisions: | Faculty of Pharmacy |
| Depositing User: | Muh Aly Mubarok |
| Date Deposited: | 18 May 2026 07:44 |
| Last Modified: | 18 May 2026 07:44 |
| URI: | https://ir.lib.ugm.ac.id/id/eprint/24271 |
