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Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells

BACKGROUND: This study determined the cytotoxic effects of root and stem bark extracts, fractions, and isolated compounds derived from Pseudocedrela kotschyi on HeLa, MCF-7, and RD cells. MATERIALS AND METHODS: The cytotoxic activity was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetr...

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Autores principales: Elufioye, Taiwo O., Abdul, Abolaji A., Moody, Jone O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330102/
https://www.ncbi.nlm.nih.gov/pubmed/28250653
http://dx.doi.org/10.4103/0974-8490.199776
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author Elufioye, Taiwo O.
Abdul, Abolaji A.
Moody, Jone O.
author_facet Elufioye, Taiwo O.
Abdul, Abolaji A.
Moody, Jone O.
author_sort Elufioye, Taiwo O.
collection PubMed
description BACKGROUND: This study determined the cytotoxic effects of root and stem bark extracts, fractions, and isolated compounds derived from Pseudocedrela kotschyi on HeLa, MCF-7, and RD cells. MATERIALS AND METHODS: The cytotoxic activity was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide colorimetric assay against three cell lines (RD, HeLa, and MCF 7) at concentrations ranging from 0.01 to 1000 μg/mL. Isolation of crude saponin was done from the most active ethyl acetate fraction and further purified using vacuum liquid chromatography and preparative thin layer chromatographic techniques. RESULTS: The cytotoxicity assay revealed that the methanol extract from the root bark and the ethyl acetate fraction from the stem bark exhibited marked anticancer activity with IC(50) of 87.36 μg/ml and 21.53 μg/ml, respectively, on HeLa cancer cell line and 101.51 μg/mL and 38.46 μg/mL, respectively, on RD cell line. These values are comparable with that obtained from vinblastine and methotrexate used as standard drugs (IC(50) values of 0.01 μg/mL and 0.05 μg/mL, respectively). The isolated crude saponins also gave IC(50) values of 5.28 μg/mL and 81.52 μg/mL against the RD cell lines and IC(50)values of 1.05 μg/mL and 86.8 μg/mL for the MCF 7 cancer cell lines. PTLC led to the isolation of a compound from the crude saponin which was identified as 7-deacetoxy-7-oxogedunin through spectroscopic analysis and comparison with literature data. CONCLUSIONS: P. kotschyi could be considered as a potential source of chemotherapeutic agent. However, further research to determine the exact mechanism of action needs to be carried out. SUMMARY: Pseudocedrela kotschyi methanol extract from the root bark and the ethyl acetate fraction from the stem bark exhibited marked anticancer activity on HeLa, MCF-7, and RD cell lines; 7-deacetoxy-7-oxogedunin isolated as a white crystalline substance from the most active ethyl acetate fraction contributed to the observed activity. [Image: see text] Abbreviations Used: MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; TLC: Thin layer chromatography; VLC: Vacuum liquid chromatography; PTLC: Preparative thin layer chromatographic; NMR: Nuclear magnetic resonance; FBS: Fetal bovine serum; DMEM: Dulbecco's modified Eagle's medium; PBS: Phosphate buffer saline; FHI: Forest Herbarium Ibadan; DMSO: Dimethylsuphoxide; SEM: Standard error of mean
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spelling pubmed-53301022017-03-01 Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells Elufioye, Taiwo O. Abdul, Abolaji A. Moody, Jone O. Pharmacognosy Res Original Article BACKGROUND: This study determined the cytotoxic effects of root and stem bark extracts, fractions, and isolated compounds derived from Pseudocedrela kotschyi on HeLa, MCF-7, and RD cells. MATERIALS AND METHODS: The cytotoxic activity was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide colorimetric assay against three cell lines (RD, HeLa, and MCF 7) at concentrations ranging from 0.01 to 1000 μg/mL. Isolation of crude saponin was done from the most active ethyl acetate fraction and further purified using vacuum liquid chromatography and preparative thin layer chromatographic techniques. RESULTS: The cytotoxicity assay revealed that the methanol extract from the root bark and the ethyl acetate fraction from the stem bark exhibited marked anticancer activity with IC(50) of 87.36 μg/ml and 21.53 μg/ml, respectively, on HeLa cancer cell line and 101.51 μg/mL and 38.46 μg/mL, respectively, on RD cell line. These values are comparable with that obtained from vinblastine and methotrexate used as standard drugs (IC(50) values of 0.01 μg/mL and 0.05 μg/mL, respectively). The isolated crude saponins also gave IC(50) values of 5.28 μg/mL and 81.52 μg/mL against the RD cell lines and IC(50)values of 1.05 μg/mL and 86.8 μg/mL for the MCF 7 cancer cell lines. PTLC led to the isolation of a compound from the crude saponin which was identified as 7-deacetoxy-7-oxogedunin through spectroscopic analysis and comparison with literature data. CONCLUSIONS: P. kotschyi could be considered as a potential source of chemotherapeutic agent. However, further research to determine the exact mechanism of action needs to be carried out. SUMMARY: Pseudocedrela kotschyi methanol extract from the root bark and the ethyl acetate fraction from the stem bark exhibited marked anticancer activity on HeLa, MCF-7, and RD cell lines; 7-deacetoxy-7-oxogedunin isolated as a white crystalline substance from the most active ethyl acetate fraction contributed to the observed activity. [Image: see text] Abbreviations Used: MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; TLC: Thin layer chromatography; VLC: Vacuum liquid chromatography; PTLC: Preparative thin layer chromatographic; NMR: Nuclear magnetic resonance; FBS: Fetal bovine serum; DMEM: Dulbecco's modified Eagle's medium; PBS: Phosphate buffer saline; FHI: Forest Herbarium Ibadan; DMSO: Dimethylsuphoxide; SEM: Standard error of mean Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5330102/ /pubmed/28250653 http://dx.doi.org/10.4103/0974-8490.199776 Text en Copyright: © 2017 Pharmacognosy Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Elufioye, Taiwo O.
Abdul, Abolaji A.
Moody, Jone O.
Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells
title Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells
title_full Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells
title_fullStr Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells
title_full_unstemmed Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells
title_short Cytotoxicity Studies of the Extracts, Fractions, and Isolated Compound of Pseudocedrela kotschyi on Cervical Cancer (HeLa), Breast Cancer (MCF-7) and Skeletal Muscle Cancer (RD) Cells
title_sort cytotoxicity studies of the extracts, fractions, and isolated compound of pseudocedrela kotschyi on cervical cancer (hela), breast cancer (mcf-7) and skeletal muscle cancer (rd) cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330102/
https://www.ncbi.nlm.nih.gov/pubmed/28250653
http://dx.doi.org/10.4103/0974-8490.199776
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