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Anticancer activity of flavonoids isolated from Achyrocline satureioides in gliomas cell lines

Authors :
Caroline Peres Klein
Priscila Oliveira de Souza
Fabrício Figueiró
Luana Heimfarth
Rosângela Mayer Gonçalves
Valquiria Linck Bassani
Juliana Bender Hoppe
Karla Suzana Moresco
José Cláudio Fonseca Moreira
Christianne Gazzana Salbego
Sara Elis Bianchi
Alfeu Zanotto Filho
Daniel Pens Gelain
Source :
Toxicology in Vitro. 51:23-33
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Achyrocline satureioides, popularly known as "marcela", is a medicinal plant found in South America. This plant is rich in flavonoids, which have been reported to exert numerous biological activities. The aim of this study was to purify, identify and evaluate the mechanisms underlining anticancer activity of A. satureioides flavonoids in glioma cell lines (U87, U251 and C6) as well as their comparative toxicity in normal brain cells (primary astrocytes, neurons and organotypic hippocampal cultures). The main flavonoids present in A. satureioides are luteolin, quercetin, 3-O-methyl-quercetin and achyrobichalcone, the later a very unique metabolite present in this plant. Isolated flavonoids as well as A. satureioides extracts reduced proliferation and clonogenic survival, and induced apoptosis of glioma cell lines. In addition, A. satureioides flavonoids potentiated the cytotoxic effect and apoptosis induction by the glioma chemotherapeutic temozolomide (TMZ). Importantly, A. satureioides flavonoids were less cytotoxic to astrocytes, neuron:astrocytes co-cultures and hippocampal cultures if compared to gliomas. Investigation of 10 cancer-related pathways showed a reduced activation of MYC and the Map kinases ERK and JNK by A. satureioides flavonoid-enriched extract, an effect not observed when individual flavonoids were evaluated. Altogether, the herein presented results show that A. satureioides extract possesses a combination of flavonoids, some unique for this plant, which have synergistic anticancer activity and potential for further studies in vivo.

Details

ISSN :
08872333
Volume :
51
Database :
OpenAIRE
Journal :
Toxicology in Vitro
Accession number :
edsair.doi.dedup.....943fc1eac19969312187854524a29293
Full Text :
https://doi.org/10.1016/j.tiv.2018.04.013