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Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines
Callerya speciosa is widely distributed in tropical and subtropical countries and is traditionally used for preventing numerous disorders. In this study, a bioguided fractionation of ethyl acetate extract (SE) from C. speciosa root was carried out to target antioxidant and cytotoxic activities. Of t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000591/ https://www.ncbi.nlm.nih.gov/pubmed/35408721 http://dx.doi.org/10.3390/molecules27072322 |
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author | Lam, Vu Quang Anh, La Hoang Quan, Nguyen Van Xuan, Tran Dang Hanamura, Ichiro Uchino, Kaori Karnan, Sivasundaram Takami, Akiyoshi |
author_facet | Lam, Vu Quang Anh, La Hoang Quan, Nguyen Van Xuan, Tran Dang Hanamura, Ichiro Uchino, Kaori Karnan, Sivasundaram Takami, Akiyoshi |
author_sort | Lam, Vu Quang |
collection | PubMed |
description | Callerya speciosa is widely distributed in tropical and subtropical countries and is traditionally used for preventing numerous disorders. In this study, a bioguided fractionation of ethyl acetate extract (SE) from C. speciosa root was carried out to target antioxidant and cytotoxic activities. Of the four fractions (SE1-SE4) obtained by column chromatography, SE4 had the strongest anti-radical ability in the DPPH and ABTS assays (IC(50) = 0.05 and 0.17 mg/mL, respectively), with results close to butylated hydroxytoluene (BHT), a common antioxidant agent. The cytotoxic activities against the selected cells were analyzed in this study by MTT assay. Accordingly, SE2, SE3, and SE4 significantly inhibited the viability of multiple myeloma cell lines, comprising U266 (IC(50) = 0.38, 0.09, and 0.11 mg/mL, respectively) and KMS11 (IC(50) = 0.09, 0.17, and 0.15 mg/mL, respectively), mantle cell lymphoma Mino (IC(50) = 0.08, 0.16, and 0.15 mg/mL, respectively), and the noncancerous cell line LCL (IC(50) = 0.40, 0.32, and 0.21 mg/mL, respectively). At a concentration of 125 µg/mL, SE2, SE3, and SE4 induced the cell apoptosis of U266 (32.2%, 53.2%, and 55.6%, respectively), KMS11 (36.9%, 40.8%, and 47.9%, respectively), Mino (36.6%, 39.8%, and 22.0%, respectively), and LCL (12.4%, 17.5%, and 23.5%, respectively) via annexin V assay. The dominant compounds detected in fractions by high-performance liquid chromatography–electrospray ionization–tandem mass spectrometry (HPLC-ESI-MS/MS), were identified as isoflavones. This is the first report describing C. speciosa as a promising natural source of antileukemia and antimyeloma agents, which may be useful for the development of blood cancer treatments. |
format | Online Article Text |
id | pubmed-9000591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90005912022-04-12 Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines Lam, Vu Quang Anh, La Hoang Quan, Nguyen Van Xuan, Tran Dang Hanamura, Ichiro Uchino, Kaori Karnan, Sivasundaram Takami, Akiyoshi Molecules Article Callerya speciosa is widely distributed in tropical and subtropical countries and is traditionally used for preventing numerous disorders. In this study, a bioguided fractionation of ethyl acetate extract (SE) from C. speciosa root was carried out to target antioxidant and cytotoxic activities. Of the four fractions (SE1-SE4) obtained by column chromatography, SE4 had the strongest anti-radical ability in the DPPH and ABTS assays (IC(50) = 0.05 and 0.17 mg/mL, respectively), with results close to butylated hydroxytoluene (BHT), a common antioxidant agent. The cytotoxic activities against the selected cells were analyzed in this study by MTT assay. Accordingly, SE2, SE3, and SE4 significantly inhibited the viability of multiple myeloma cell lines, comprising U266 (IC(50) = 0.38, 0.09, and 0.11 mg/mL, respectively) and KMS11 (IC(50) = 0.09, 0.17, and 0.15 mg/mL, respectively), mantle cell lymphoma Mino (IC(50) = 0.08, 0.16, and 0.15 mg/mL, respectively), and the noncancerous cell line LCL (IC(50) = 0.40, 0.32, and 0.21 mg/mL, respectively). At a concentration of 125 µg/mL, SE2, SE3, and SE4 induced the cell apoptosis of U266 (32.2%, 53.2%, and 55.6%, respectively), KMS11 (36.9%, 40.8%, and 47.9%, respectively), Mino (36.6%, 39.8%, and 22.0%, respectively), and LCL (12.4%, 17.5%, and 23.5%, respectively) via annexin V assay. The dominant compounds detected in fractions by high-performance liquid chromatography–electrospray ionization–tandem mass spectrometry (HPLC-ESI-MS/MS), were identified as isoflavones. This is the first report describing C. speciosa as a promising natural source of antileukemia and antimyeloma agents, which may be useful for the development of blood cancer treatments. MDPI 2022-04-03 /pmc/articles/PMC9000591/ /pubmed/35408721 http://dx.doi.org/10.3390/molecules27072322 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lam, Vu Quang Anh, La Hoang Quan, Nguyen Van Xuan, Tran Dang Hanamura, Ichiro Uchino, Kaori Karnan, Sivasundaram Takami, Akiyoshi Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines |
title | Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines |
title_full | Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines |
title_fullStr | Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines |
title_full_unstemmed | Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines |
title_short | Cytotoxicity of Callerya speciosa Fractions against Myeloma and Lymphoma Cell Lines |
title_sort | cytotoxicity of callerya speciosa fractions against myeloma and lymphoma cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000591/ https://www.ncbi.nlm.nih.gov/pubmed/35408721 http://dx.doi.org/10.3390/molecules27072322 |
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