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Cytotoxic Compounds from Wrightia pubescens (R.Br.)

BACKGROUND: Mixtures of ursolic acid (1) and oleanolic acid (2) (1:1 and 1:2), oleanolic acid (2), squalene (3), chlorophyll a (4), wrightiadione (5), and α-amyrin acetate (6) were isolated from the dichloromethane (CH(2) Cl(2)) extracts of the leaves and twigs of Wrightia pubescens (R.Br.). OBJECTI...

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Autores principales: De Los Reyes, Mariquit M., Oyong, Glenn G., S. Ng, Vincent Antonio, Shen, Chien-Chang, Ragasa, Consolacion Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855380/
https://www.ncbi.nlm.nih.gov/pubmed/29568181
http://dx.doi.org/10.4103/pr.pr_45_17
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author De Los Reyes, Mariquit M.
Oyong, Glenn G.
S. Ng, Vincent Antonio
Shen, Chien-Chang
Ragasa, Consolacion Y.
author_facet De Los Reyes, Mariquit M.
Oyong, Glenn G.
S. Ng, Vincent Antonio
Shen, Chien-Chang
Ragasa, Consolacion Y.
author_sort De Los Reyes, Mariquit M.
collection PubMed
description BACKGROUND: Mixtures of ursolic acid (1) and oleanolic acid (2) (1:1 and 1:2), oleanolic acid (2), squalene (3), chlorophyll a (4), wrightiadione (5), and α-amyrin acetate (6) were isolated from the dichloromethane (CH(2) Cl(2)) extracts of the leaves and twigs of Wrightia pubescens (R.Br.). OBJECTIVES: To test for the cytotoxicity potentials of 1–6. MATERIALS AND METHODS: The antiproliferative activities of 1–6 against three human cancer cell lines, breast (MCF-7) and colon (HT-29 and HCT-116), and a normal cell line, human dermal fibroblast neonatal (HDFn), were evaluated using the PrestoBlue(®) cell viability assay. RESULTS: Compounds 4, 1 and 2 (1:2), 2, 1 and 2 (1:1), and 5 exhibited the most cytotoxic effects against HT-29 with half maximal inhibitory concentration (IC(50)) values of 0.68, 0.74, 0.89, 1.70, and 4.07 μg/mL, respectively. Comparing 2 with its 1:1 mixture with 1 (IC(50) = 1.70 and 7.18 μg/mL for HT-29 and HCT-116, respectively) and 1:2 mixture with 1 (0.74 and 3.46 μg/mL for HT-29 and HCT-116, respectively), 2 also showed strong cytotoxic potential against HT-29 and HCT-116 (0.89 and 2.33 μg/mL, respectively). Unlike the mixtures which exhibited low effects on MCF-7 (IC(50) = 20.75 and 30.06 μg/mL for 1:1 and 1:2, respectively), 2 showed moderate activity against MCF-7 (10.99 μg/mL). Compound 6 showed the highest cytotoxicity against HCT-116 (IC(50) = 4.07 μg/mL). CONCLUSION: Mixtures of 1 and 2 (1:1 and 1:2), 2, 3, 4, 5, and 6 from the CH(2) Cl(2) extracts of the leaves and twigs of W. pubescens (R.Br.) exhibited varying cytotoxic activities. All the compounds except 6 exhibited the strongest cytotoxic effects against HT-29. On the other hand, 6 was most cytotoxic against HCT-116. Overall, the toxicities of 1–6 were highest against HT-29, followed by HCT-116 and MCF-7. All the compounds showed varying activities against HDFn (IC(50) < 30 μg/mL). SUMMARY: Mixtures of ursolic acid (1) and oleanolic acid (2) (1:1 and 1:2), oleanolic acid (2), squalene (3), chlorophyll a (4), wrightiadione (5), and α-amyrin acetate (6), isolated from the dichloromethane extracts of the leaves and twigs of Wrightia pubescens (R.Br.), showed varying cytotoxic activities against three human cancer cell lines, breast (MCF-7) and colon (HT-29 and HCT-116), and a normal cell line, human dermal fibroblast-neonatal (HDFn), as evaluated using the PrestoBlue(®) cell viability assay. [Image: see text] Abbreviation Used: IC(50): Half maximal inhibitory concentration.
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spelling pubmed-58553802018-03-22 Cytotoxic Compounds from Wrightia pubescens (R.Br.) De Los Reyes, Mariquit M. Oyong, Glenn G. S. Ng, Vincent Antonio Shen, Chien-Chang Ragasa, Consolacion Y. Pharmacognosy Res Original Article BACKGROUND: Mixtures of ursolic acid (1) and oleanolic acid (2) (1:1 and 1:2), oleanolic acid (2), squalene (3), chlorophyll a (4), wrightiadione (5), and α-amyrin acetate (6) were isolated from the dichloromethane (CH(2) Cl(2)) extracts of the leaves and twigs of Wrightia pubescens (R.Br.). OBJECTIVES: To test for the cytotoxicity potentials of 1–6. MATERIALS AND METHODS: The antiproliferative activities of 1–6 against three human cancer cell lines, breast (MCF-7) and colon (HT-29 and HCT-116), and a normal cell line, human dermal fibroblast neonatal (HDFn), were evaluated using the PrestoBlue(®) cell viability assay. RESULTS: Compounds 4, 1 and 2 (1:2), 2, 1 and 2 (1:1), and 5 exhibited the most cytotoxic effects against HT-29 with half maximal inhibitory concentration (IC(50)) values of 0.68, 0.74, 0.89, 1.70, and 4.07 μg/mL, respectively. Comparing 2 with its 1:1 mixture with 1 (IC(50) = 1.70 and 7.18 μg/mL for HT-29 and HCT-116, respectively) and 1:2 mixture with 1 (0.74 and 3.46 μg/mL for HT-29 and HCT-116, respectively), 2 also showed strong cytotoxic potential against HT-29 and HCT-116 (0.89 and 2.33 μg/mL, respectively). Unlike the mixtures which exhibited low effects on MCF-7 (IC(50) = 20.75 and 30.06 μg/mL for 1:1 and 1:2, respectively), 2 showed moderate activity against MCF-7 (10.99 μg/mL). Compound 6 showed the highest cytotoxicity against HCT-116 (IC(50) = 4.07 μg/mL). CONCLUSION: Mixtures of 1 and 2 (1:1 and 1:2), 2, 3, 4, 5, and 6 from the CH(2) Cl(2) extracts of the leaves and twigs of W. pubescens (R.Br.) exhibited varying cytotoxic activities. All the compounds except 6 exhibited the strongest cytotoxic effects against HT-29. On the other hand, 6 was most cytotoxic against HCT-116. Overall, the toxicities of 1–6 were highest against HT-29, followed by HCT-116 and MCF-7. All the compounds showed varying activities against HDFn (IC(50) < 30 μg/mL). SUMMARY: Mixtures of ursolic acid (1) and oleanolic acid (2) (1:1 and 1:2), oleanolic acid (2), squalene (3), chlorophyll a (4), wrightiadione (5), and α-amyrin acetate (6), isolated from the dichloromethane extracts of the leaves and twigs of Wrightia pubescens (R.Br.), showed varying cytotoxic activities against three human cancer cell lines, breast (MCF-7) and colon (HT-29 and HCT-116), and a normal cell line, human dermal fibroblast-neonatal (HDFn), as evaluated using the PrestoBlue(®) cell viability assay. [Image: see text] Abbreviation Used: IC(50): Half maximal inhibitory concentration. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5855380/ /pubmed/29568181 http://dx.doi.org/10.4103/pr.pr_45_17 Text en Copyright: © 2018 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
De Los Reyes, Mariquit M.
Oyong, Glenn G.
S. Ng, Vincent Antonio
Shen, Chien-Chang
Ragasa, Consolacion Y.
Cytotoxic Compounds from Wrightia pubescens (R.Br.)
title Cytotoxic Compounds from Wrightia pubescens (R.Br.)
title_full Cytotoxic Compounds from Wrightia pubescens (R.Br.)
title_fullStr Cytotoxic Compounds from Wrightia pubescens (R.Br.)
title_full_unstemmed Cytotoxic Compounds from Wrightia pubescens (R.Br.)
title_short Cytotoxic Compounds from Wrightia pubescens (R.Br.)
title_sort cytotoxic compounds from wrightia pubescens (r.br.)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855380/
https://www.ncbi.nlm.nih.gov/pubmed/29568181
http://dx.doi.org/10.4103/pr.pr_45_17
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