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https://hdl.handle.net/10216/120413Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.creator | Prata-Sena M. | |
| dc.creator | Ramos A.A. | |
| dc.creator | Buttachon S. | |
| dc.creator | Castro-Carvalho B. | |
| dc.creator | Marques P. | |
| dc.creator | Dethoup T. | |
| dc.creator | Kijjoa A. | |
| dc.creator | Rocha E. | |
| dc.date.accessioned | 2019-05-31T16:15:32Z | - |
| dc.date.available | 2019-05-31T16:15:32Z | - |
| dc.date.issued | 2016 | |
| dc.identifier.issn | 0951418X, 10991573 | |
| dc.identifier.uri | https://hdl.handle.net/10216/120413 | - |
| dc.description.abstract | Compounds isolated from the marine sea fan-derived fungus Neosartorya siamensis (KUFA 0017), namely, 2,4-dihydroxy-3-methylacetophenon (1), chevalone C (2), nortryptoquivaline (4), tryptoquivaline H (6), tryptoquivaline F (7), fiscalin A (8), epi-fiscalin A (9), epi-neofiscalin A (11) and epi-fiscalin C (13) were tested for anti-proliferative activity by MTT assay, DNA damage induction by comet assay, and induction of cell death by nuclear condensation assay on colon HCT116, liver HepG2 and melanoma A375 cancer cell lines. Compounds 2, 4, 8, 9, 11 and 13 presented IC50 values ranging from 24 to 153 μM in the selected cell lines. Cell death was induced in HCT116 by compounds 2, 4 and 8. In HepG2, compounds 4, 8, 9 and 11 were able to induce significant cell death. This induction of cell death is possibly not related to genotoxicity because none of the compounds induced significant DNA damage. These results suggest that selected compounds present an interesting anti-proliferative activity and cell death induction, consequently showing potential (specifically epi-fiscalin C) as future leads for chemotherapeutic agents. Further studies on mechanisms of action should ensue. Copyright © 2016 John Wiley & Sons, Copyright © 2016 John Wiley & Sons, | |
| dc.description.sponsorship | This research was partially financed by the Research Line NOVELMAR – novel marine products with biotechnological applications, integrated in the Structured Program of R&D&I INNOVMAR – Innovation and Sustainability in the Management and Exploitation of Marine Resources (reference NORTE‐01‐0145‐FEDER‐000035), funded by the Northern Regional Operational Programme (NORTE2020) through the European Regional Development Fund (ERDF). The CIIMAR is supported by ERDF, via COMPETE – Operational Competitiveness Programme, and by public funds via Foundation for Science and Technology (FCT), contract UID/Multi/04423/2013. We thank ICBAS for partially funding the work of M. Prata Sena and B. Castro Carvalho, namely as students of the Master in Marine Sciences – Marine Resources. | |
| dc.language.iso | eng | |
| dc.publisher | John Wiley and Sons | |
| dc.relation | info:eu-repo/grantAgreement/FCT/5876/147268/PT | |
| dc.relation.ispartof | Phytotherapy Research, vol. 30(11), p. 1862-1871 | |
| dc.rights | restrictedAccess | |
| dc.title | Cytotoxic activity of Secondary Metabolites from Marine-derived Fungus Neosartorya siamensis in Human Cancer Cells | |
| dc.type | Artigo em Revista Científica Internacional | |
| dc.contributor.uporto | CIIMAR - Centro Interdisciplinar de Investigação Marinha e Ambiental | |
| dc.identifier.doi | 10.1002/ptr.5696 | |
| dc.relation.publisherversion | http://dx.doi.org/10.1002/ptr.5696 | |
| Appears in Collections: | CIIMAR - Artigo em Revista Científica Internacional | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Prata-Sena M_2016.pdf Restricted Access | 527.31 kB | Adobe PDF | View/Open |
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