Croton gratissimus leaf extracts inhibit cancer cell growth by inducing caspase 3/7 activation with additional anti-inflammatory and antioxidant activities
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Date
Authors
Njoya, Emmanuel Mfotie
Eloff, Jacobus Nicolaas
McGaw, Lyndy Joy
Journal Title
Journal ISSN
Volume Title
Publisher
BioMed Central
Abstract
BACKGROUND : Croton species (Euphorbiaceae) are distributed in different parts of the world, and are used in
traditional medicine to treat various ailments including cancer, inflammation, parasitic infections and oxidative stress
related diseases. The present study aimed to evaluate the antioxidant, anti-inflammatory and cytotoxic properties of
different extracts from three Croton species.
METHODS : Acetone, ethanol and water leaf extracts from C. gratissimus, C. pseudopulchellus, and C. sylvaticus were
tested for their free radical scavenging activity. Anti-inflammatory activity was determined via the nitric oxide (NO)
inhibitory assay on lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages, and the 15-lipoxygenase inhibitory
assay using the ferrous oxidation-xylenol orange assay. The cytotoxicity of the extracts was determined on four
cancerous cell lines (A549, Caco-2, HeLa, MCF-7), and a non-cancerous African green monkey (Vero) kidney cells
using the tetrazolium-based colorimetric (MTT) assay. The potential mechanism of action of the active extracts was
explored by quantifying the caspase-3/− 7 activity with the Caspase-Glo® 3/7 assay kit (Promega).
RESULTS : The acetone and ethanol leaf extracts of C. pseudopulchellus and C. sylvaticus were highly cytotoxic to the
non-cancerous cells with LC50 varying between 7.86 and 48.19 μg/mL. In contrast, the acetone and ethanol extracts
of C. gratissimus were less cytotoxic to non-cancerous cells and more selective with LC50 varying between 152.30
and 462.88 μg/mL, and selectivity index (SI) ranging between 1.56 and 11.64. Regarding the anti-inflammatory
activity, the acetone leaf extract of C. pseudopulchellus had the highest NO inhibitory potency with an IC50 of 34.
64 μg/mL, while the ethanol leaf extract of the same plant was very active against 15-lipoxygenase with an IC50 of
0.57 μg/mL. A linear correlation (r<0.5) was found between phytochemical contents, antioxidant, anti-inflammatory
and cytotoxic activities of active extracts. These extracts induced differentially the activation of caspases − 3 and − 7
enzymes in all the four cancerous cells with the highest induction (1.83-fold change) obtained on HeLa cells with
the acetone leaf extract of C. gratissimus.
CONCLUSION : Based on their selective toxicity, good antioxidant and anti-inflammatory activities, the acetone and
ethanol leaf extracts of C. gratissimus represent promising alternative sources of compounds against cancer and
other oxidative stress related diseases.
Description
Additional file 1: Figure S1. Non-linear regression curves for IC50 determination
of different extracts from Croton species in 15-lipoxygenase
(15-LOX) inhibitory assay. CSA and CSE represent respectively acetone,
ethanol and water extracts of Croton sylvaticus. CGA and CGE represent
respectively acetone, ethanol and water extracts of Croton gratissimus.
CPA and CPE represent respectively acetone, ethanol and water extracts
of Croton pseudopulchellus.
Additional file 2: Figure S2. Concentration-dependent graph of A549 cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 3: Figure S3. Concentration-dependent graph of Caco-2 cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 4: Figure S4. Concentration-dependent graph of HeLa cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 5: Figure S5. Concentration-dependent graph of MCF-7 cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 6: Figure S6. Concentration-dependent graph of Vero cell viability of different extracts from Croton species. Extracts were tested at concentrations between 1000 and 50 μg/mL Ctrl: 0.5% DMSO.
Additional file 2: Figure S2. Concentration-dependent graph of A549 cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 3: Figure S3. Concentration-dependent graph of Caco-2 cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 4: Figure S4. Concentration-dependent graph of HeLa cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 5: Figure S5. Concentration-dependent graph of MCF-7 cell viability of different extracts from Croton species. Extracts were tested at concentrations between 200 and 6.25 μg/mL; Ctrl: 0.5% DMSO.
Additional file 6: Figure S6. Concentration-dependent graph of Vero cell viability of different extracts from Croton species. Extracts were tested at concentrations between 1000 and 50 μg/mL Ctrl: 0.5% DMSO.
Keywords
Croton gratissimus, Free radicals, Nitric oxide, 15-Lipoxygenase, Cytotoxicity, Caspases
Sustainable Development Goals
Citation
Njoya, E.M., Eloff, J.N. & McGaw, L.J. 2018, 'Croton gratissimus leaf extracts inhibit cancer cell growth by inducing caspase 3/7 activation with additional anti-inflammatory and antioxidant activities', BMC Complementary and Alternative Medicine, vol. 18, art. 305, pp. 1-11.