Cytotoxicity induced by extracts of pisolithus tinctorius spores on human cancer and normal cell lines - evaluation of the anticancer potential

Ricardo Alves, Marco Preto, Vitor Vasconcelos, Rui S. Oliveira, Rosário Martins*

*Corresponding author for this work

Research output: Contribution to journalConference articlepeer-review

5 Citations (Scopus)

Abstract

Fungi have been considered a potential source of natural anticancer drugs. However, studies on these organisms have mainly focused on compounds present in the sporocarp and mycelium. The aim of this study was to assess the anticancer potential of fungal spores using a bioassay-guided fractionation with cancer and normal cell lines. Crude extracts from spores of the basidiomycetous fungus Pisolithus tinctorius were prepared using five solvents/solvent mixtures in order to select the most effective crude extraction procedure. A dichloromethane/methanol (DCM/MeOH) mixture was found to produce the highest extraction yield, and this extract was fractionated into 11 fractions. Crude extracts and fractions were assayed for cytotoxicity in the human osteocarcinoma cell line MG63, the human breast carcinoma cell line T47D, the human colon adenocarcinoma cell line RKO, and the normal human brain capillary endothelial cell line hCMEC/D3. Cytotoxicity was assessed by the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) reduction assay. The results showed a reduction in cancer cell viability of approximately 95% with 4 of 11 fractions without a significant reduction in viability of hCMEC/D3 cells. Data demonstrated that spores of P. tinctorius might serve as an interesting source of compounds with potential anticancer properties.
Original languageEnglish
Pages (from-to)840-847
Number of pages8
JournalJournal of Toxicology and Environmental Health - Part A: Current Issues
Volume78
Issue number13-14
DOIs
Publication statusPublished - 18 Jul 2015
Event3rd International Congress on Environmental Health - Instituto Politécnico do Porto, Porto, Portugal
Duration: 1 Sept 20141 Sept 2014

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