Croton gratissimus leaf extracts inhibit cancer cell growth by inducing caspase 3/7 activation with additional anti-inflammatory and antioxidant activities

dc.contributor.authorNjoya, Emmanuel Mfotie
dc.contributor.authorEloff, Jacobus Nicolaas
dc.contributor.authorMcGaw, Lyndy Joy
dc.date.accessioned2019-10-10T08:41:23Z
dc.date.available2019-10-10T08:41:23Z
dc.date.issued2018-11-14
dc.descriptionAdditional 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.en_ZA
dc.descriptionAdditional 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.en_ZA
dc.descriptionAdditional 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.en_ZA
dc.descriptionAdditional 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.en_ZA
dc.descriptionAdditional 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.en_ZA
dc.descriptionAdditional 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.en_ZA
dc.description.abstractBACKGROUND : 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.en_ZA
dc.description.departmentParaclinical Sciencesen_ZA
dc.description.librarianam2019en_ZA
dc.description.sponsorshipThe National Research Foundation (NRF), South Africa through the Incentive Funding for Rated Researchers (Lyndy J. McGaw).en_ZA
dc.description.urihttps://bmccomplementalternmed.biomedcentral.comen_ZA
dc.identifier.citationNjoya, 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.en_ZA
dc.identifier.issn10.1186/s12906-018-2372-9
dc.identifier.issn1472-6882 (online)
dc.identifier.urihttp://hdl.handle.net/2263/71784
dc.language.isoenen_ZA
dc.publisherBioMed Centralen_ZA
dc.rights© The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License.en_ZA
dc.subjectCroton gratissimusen_ZA
dc.subjectFree radicalsen_ZA
dc.subjectNitric oxideen_ZA
dc.subject15-Lipoxygenaseen_ZA
dc.subjectCytotoxicityen_ZA
dc.subjectCaspasesen_ZA
dc.titleCroton gratissimus leaf extracts inhibit cancer cell growth by inducing caspase 3/7 activation with additional anti-inflammatory and antioxidant activitiesen_ZA
dc.typeArticleen_ZA

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