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The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells

Linusorbs (LOs) are natural peptides found in flaxseed oil that exert various biological activities. Of LOs, LOB3 ([1–9-NαC]-linusorb B3) was reported to have antioxidative and anti-inflammatory activities; however, its anti-cancer activity has been poorly understood. Therefore, this study investiga...

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Autores principales: Sung, Nak Yoon, Jeong, Deok, Shim, Youn Young, Ratan, Zubair Ahmed, Jang, Young-Jin, Reaney, Martin J. T., Lee, Sarah, Lee, Byoung-Hee, Kim, Jong-Hoon, Yi, Young-Su, Cho, Jae Youl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7764463/
https://www.ncbi.nlm.nih.gov/pubmed/33322712
http://dx.doi.org/10.3390/molecules25245881
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author Sung, Nak Yoon
Jeong, Deok
Shim, Youn Young
Ratan, Zubair Ahmed
Jang, Young-Jin
Reaney, Martin J. T.
Lee, Sarah
Lee, Byoung-Hee
Kim, Jong-Hoon
Yi, Young-Su
Cho, Jae Youl
author_facet Sung, Nak Yoon
Jeong, Deok
Shim, Youn Young
Ratan, Zubair Ahmed
Jang, Young-Jin
Reaney, Martin J. T.
Lee, Sarah
Lee, Byoung-Hee
Kim, Jong-Hoon
Yi, Young-Su
Cho, Jae Youl
author_sort Sung, Nak Yoon
collection PubMed
description Linusorbs (LOs) are natural peptides found in flaxseed oil that exert various biological activities. Of LOs, LOB3 ([1–9-NαC]-linusorb B3) was reported to have antioxidative and anti-inflammatory activities; however, its anti-cancer activity has been poorly understood. Therefore, this study investigated the anti-cancer effect of LOB3 and its underlying mechanism in glioblastoma cells. LOB3 induced apoptosis and suppressed the proliferation of C6 cells by inhibiting the expression of anti-apoptotic genes, B cell lymphoma 2 (Bcl-2) and p53, as well as promoting the activation of pro-apoptotic caspases, caspase-3 and -9. LOB3 also retarded the migration of C6 cells, which was achieved by suppressing the formation of the actin cytoskeleton critical for the progression, invasion, and metastasis of cancer. Moreover, LOB3 inhibited the activation of the proto-oncogene, Src, and the downstream effector, signal transducer and activator of transcription 3 (STAT3), in C6 cells. Taken together, these results suggest that LOB3 plays an anti-cancer role by inducing apoptosis and inhibiting the migration of C6 cells through the regulation of apoptosis-related molecules, actin polymerization, and proto-oncogenes.
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spelling pubmed-77644632020-12-27 The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells Sung, Nak Yoon Jeong, Deok Shim, Youn Young Ratan, Zubair Ahmed Jang, Young-Jin Reaney, Martin J. T. Lee, Sarah Lee, Byoung-Hee Kim, Jong-Hoon Yi, Young-Su Cho, Jae Youl Molecules Article Linusorbs (LOs) are natural peptides found in flaxseed oil that exert various biological activities. Of LOs, LOB3 ([1–9-NαC]-linusorb B3) was reported to have antioxidative and anti-inflammatory activities; however, its anti-cancer activity has been poorly understood. Therefore, this study investigated the anti-cancer effect of LOB3 and its underlying mechanism in glioblastoma cells. LOB3 induced apoptosis and suppressed the proliferation of C6 cells by inhibiting the expression of anti-apoptotic genes, B cell lymphoma 2 (Bcl-2) and p53, as well as promoting the activation of pro-apoptotic caspases, caspase-3 and -9. LOB3 also retarded the migration of C6 cells, which was achieved by suppressing the formation of the actin cytoskeleton critical for the progression, invasion, and metastasis of cancer. Moreover, LOB3 inhibited the activation of the proto-oncogene, Src, and the downstream effector, signal transducer and activator of transcription 3 (STAT3), in C6 cells. Taken together, these results suggest that LOB3 plays an anti-cancer role by inducing apoptosis and inhibiting the migration of C6 cells through the regulation of apoptosis-related molecules, actin polymerization, and proto-oncogenes. MDPI 2020-12-12 /pmc/articles/PMC7764463/ /pubmed/33322712 http://dx.doi.org/10.3390/molecules25245881 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sung, Nak Yoon
Jeong, Deok
Shim, Youn Young
Ratan, Zubair Ahmed
Jang, Young-Jin
Reaney, Martin J. T.
Lee, Sarah
Lee, Byoung-Hee
Kim, Jong-Hoon
Yi, Young-Su
Cho, Jae Youl
The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells
title The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells
title_full The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells
title_fullStr The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells
title_full_unstemmed The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells
title_short The Anti-Cancer Effect of Linusorb B3 from Flaxseed Oil through the Promotion of Apoptosis, Inhibition of Actin Polymerization, and Suppression of Src Activity in Glioblastoma Cells
title_sort anti-cancer effect of linusorb b3 from flaxseed oil through the promotion of apoptosis, inhibition of actin polymerization, and suppression of src activity in glioblastoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7764463/
https://www.ncbi.nlm.nih.gov/pubmed/33322712
http://dx.doi.org/10.3390/molecules25245881
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