Review Article

Medicinal Plants from Brazilian Cerrado: Antioxidant and Anticancer Potential and Protection against Chemotherapy Toxicity

Table 2

Cytotoxic potential and compounds identified from extracts of Cerrado plants.

Plant speciesParts usedModelCytotoxic featuresCompounds identifiedRef.

S. adstringensStem barkB16F10-Nex2Mitochondrial depolarization, caspase-3 activation, and ROS productionGallic acid, procyanidins, and catechinsBaldivia et al. [16]
Stem barkHeLa, SiHa, and C33AIntense oxidative stress, mitochondrial damage, increased Bax/BCL-2 ratio, and increased caspase-9 and caspase-3 expressionProanthocyanidin polymer-rich fractionKaplum et al. [146]
MCF-7 and MDA-MB-435Increased Bax/BCL-2 ratio and increased caspase-9, active caspase-3, caspase-8, LC-3, and beclin-1 expressionGallic acid, procyanidins, and catechinsSabino et al. [147]

C. adamantiumLeavesK562 cellsCaspase-3 and caspase-9 activation, cell cycle arrest at the S and G2 phases, and calcium influxO-Pentoside and O-deoxyhexoside myricetin, quercetin O-pentoside, and myricetin-O-(O-galloyl)-pentosideCampos et al. [17]
RootsO-Pentoside, O-methyl ellagic acid, O-hexoside, O-deoxyhexoside, O-methyl ellagic acid, and gallic acid
LeavesPC-3Inhibited prostate cancer cell proliferation, DNA fragmentation, and decreased NFkB1 expressionChalcone cardamoninPascoal et al. [144]
MCF-7, HeLa, and M059JInhibited cancer cell proliferationβ-Myrcene, spathulenol, germacrene-B, β-caryophyllene oxide, β-caryophyllene, α-pinene, viridiflorol, limonene, and (Z,E)-farnesol (6.51%)Alves et al. [145]

S. velutinaLeavesJurkat/K562 cellsCaspase-3 activation, mitochondrial depolarization, cell cycle arrest at the S and G2 phases, and calcium influxEpigallocatechin, epicatechin, rutin, kaempferol glycosides, and dimeric and trimeric proanthocyanidinsCampos et al. [18]
RootsB16F10nex2 cells and mouse C57b1/6Increased intracellular ROS levels, induced mitochondrial membrane potential dysfunction, activated caspase-3, and impaired pulmonary metastasis in vitroFlavonoid derivatives of catechin and piceatannol (active metabolite of resveratrol) groups and dimeric tetrahydroanthracene derivativesCastro et al. [142]

J. decurrensLeavesK562 cellsMitochondrial depolarization, Caspase-3 activation, necrosis and late apoptosisPhenolic compounds and flavonoidsCasagrande et al. [19]

H. speciosaLeavesKasumi-1 cellsNecroptosis and cathepsin releaseBornesitol, quinic acid, chlorogenic acid, and flavonoids derived from kaempferol and rutinDos Santos et al. [46]

G. ulmifoliaStem barkK562 cells and mouse C57b1/6Protected against the doxorubicin-induced cardiotoxicity and reduced oxidative haemolysis in vitroCitric and quinic acidsDos Santos et al. [22]
LeavesO-Pentosyl and di-O-deoxyhesosyl-hesosyl quercetin, O-deoxyhexosyl hexosyl luteolin, and di-O-deoxyhexosyl hexosyl kaempferol

S. terebinthifoliusLeavesK562 cells and mouse C57b1/6Protected against doxorubicin-induced cardiotoxicity and reduced oxidative haemolysis in vitroPhenolic compounds, flavonoid, tannin, and ascorbic acid [21] and α-pinene, limonene, carene, and phellandrene [159]Rocha et al. [21] and Carneiro et al. [159]