| Literature DB >> 29730415 |
Priscila Oliveira de Souza1, Sara Elis Bianchi2, Fabrício Figueiró3, Luana Heimfarth3, Karla Suzana Moresco3, Rosângela Mayer Gonçalves4, Juliana Bender Hoppe3, Caroline Peres Klein3, Christianne Gazzana Salbego3, Daniel Pens Gelain3, Valquíria Linck Bassani2, Alfeu Zanotto Filho4, José Claudio Fonseca Moreira3.
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.Entities:
Keywords: Achyrocline satureioides; Antiproliferative effect; Flavonoids; Glioblastoma multiforme
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Year: 2018 PMID: 29730415 DOI: 10.1016/j.tiv.2018.04.013
Source DB: PubMed Journal: Toxicol In Vitro ISSN: 0887-2333 Impact factor: 3.500