Toxicogenomic analysis of pharmacological active coumarins isolated from Calophyllum brasiliense

• Published in: Genomics data 2015-12, Vol.6 (C), p.258-259
• Main Authors: Gomez-Verjan, J.C., Estrella-Parra, E.A., Gonzalez-Sanchez, I., Rivero-Segura, N.A., Vazquez-Martinez, R., Magos-Guerrero, G., Mendoza-Villanueva, D., Cerbón-Cervantes, M.A., Reyes-Chilpa, R.
• Format: Article
• Language: English
• Subjects: Data in Brief
• ISSN: 2213-5960; 2213-5960
• DOI: 10.1016/j.gdata.2015.10.006

Calophyllum brasiliense (Calophyllaceae) is a tropical rain forest tree, mainly distributed in South and Central America. It is an important source of bioactive natural products like, for instance soulatrolide, and mammea type coumarins. Soulatrolide is a tetracyclic dipyranocoumarins and a potent inhibitor of HIV-1 reverse transcriptase and Mycobacterium tuberculosis. Mammea A/BA and A/BB coumarins, pure or as a mixture, are highly active against several leukemia cell lines, Trypanosoma cruzi and Leishmania amazonensis. In the present work, a toxicogenomic analysis of Soulatrolide and Mammea A/BA+A/BB (3:1) mixture was performed in order to validate the toxicological potential of this type of compounds. Soulatrolide or mixture of mammea A/BA + A/BB (3:1) was administered orally to male mice (CD-1) at dose of 100mg/kg/daily, for 1week. After this time, mice were sacrificed, and RNA extracted from the liver of treated animals. Transcriptomic analysis was performed using Affymetrix Mouse Gene 1.0 ST Array. Robust microarray analysis (RMA) and two way ANOVA test revealed for mammea mixture treatment 46 genes upregulated and 72 downregulated genes; meanwhile, for soulatrolide 665 were upregulated and 1077 downregulated genes. Enrichment analysis for such genes revealed that in both type of treatments genetic expression were mainly involved in drug metabolism. Overall results indicate a safety profile. The microarray data complies with MIAME guidelines and are deposited in GEO under accession number GSE72755.