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Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity

Rosemary extract is used in food additives and traditional medicine and has been observed to contain anti-tumor activity. In this study, rosemary extract is hypothesized to induce synthetic lethality in BRCA2 deficient cells by PARP inhibition. Chinese hamster lung V79 cells and its mutant cell line...

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Autores principales: Su, Cathy, Gius, Jeffrey P., Van Steenberg, Julia, Haskins, Alexis H., Heishima, Kazuki, Omata, Chisato, Iwayama, Masahiro, Murakami, Mami, Mori, Takashi, Maruo, Kohji, Kato, Takamitsu A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711971/
https://www.ncbi.nlm.nih.gov/pubmed/29196727
http://dx.doi.org/10.1038/s41598-017-16795-3
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author Su, Cathy
Gius, Jeffrey P.
Van Steenberg, Julia
Haskins, Alexis H.
Heishima, Kazuki
Omata, Chisato
Iwayama, Masahiro
Murakami, Mami
Mori, Takashi
Maruo, Kohji
Kato, Takamitsu A.
author_facet Su, Cathy
Gius, Jeffrey P.
Van Steenberg, Julia
Haskins, Alexis H.
Heishima, Kazuki
Omata, Chisato
Iwayama, Masahiro
Murakami, Mami
Mori, Takashi
Maruo, Kohji
Kato, Takamitsu A.
author_sort Su, Cathy
collection PubMed
description Rosemary extract is used in food additives and traditional medicine and has been observed to contain anti-tumor activity. In this study, rosemary extract is hypothesized to induce synthetic lethality in BRCA2 deficient cells by PARP inhibition. Chinese hamster lung V79 cells and its mutant cell lines, V-C8 (BRCA2 deficient) and V-C8 with BRCA2 gene correction were used. Rosemary extract and its major constituent chemicals were tested for their cytotoxicity by colony formation assay in cells of different BRCA2 status. The latter chemicals were tested for inhibitory effect of poly (ADP-ribose) polymerase (PARP) activity in vitro and in vivo. Rosemary has shown selective cytotoxicity against V-C8 cells (IC(50) 17 µg/ml) compared to V79 cells (IC(50) 26 µg/ml). Among tested chemicals, gallic acid and carnosic acid showed selective cytotoxicity to V-C8 cells along with PARP inhibitory effects. Carnosol showed comparative PARP inhibitory effects at 100 µM compared to carnosic acid and gallic acid, but the selective cytotoxicity was not observed. In conclusion, we predict that within rosemary extract two specific constituent components; gallic acid and carnosic acid were the cause for the synthetic lethality.
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spelling pubmed-57119712017-12-06 Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity Su, Cathy Gius, Jeffrey P. Van Steenberg, Julia Haskins, Alexis H. Heishima, Kazuki Omata, Chisato Iwayama, Masahiro Murakami, Mami Mori, Takashi Maruo, Kohji Kato, Takamitsu A. Sci Rep Article Rosemary extract is used in food additives and traditional medicine and has been observed to contain anti-tumor activity. In this study, rosemary extract is hypothesized to induce synthetic lethality in BRCA2 deficient cells by PARP inhibition. Chinese hamster lung V79 cells and its mutant cell lines, V-C8 (BRCA2 deficient) and V-C8 with BRCA2 gene correction were used. Rosemary extract and its major constituent chemicals were tested for their cytotoxicity by colony formation assay in cells of different BRCA2 status. The latter chemicals were tested for inhibitory effect of poly (ADP-ribose) polymerase (PARP) activity in vitro and in vivo. Rosemary has shown selective cytotoxicity against V-C8 cells (IC(50) 17 µg/ml) compared to V79 cells (IC(50) 26 µg/ml). Among tested chemicals, gallic acid and carnosic acid showed selective cytotoxicity to V-C8 cells along with PARP inhibitory effects. Carnosol showed comparative PARP inhibitory effects at 100 µM compared to carnosic acid and gallic acid, but the selective cytotoxicity was not observed. In conclusion, we predict that within rosemary extract two specific constituent components; gallic acid and carnosic acid were the cause for the synthetic lethality. Nature Publishing Group UK 2017-12-01 /pmc/articles/PMC5711971/ /pubmed/29196727 http://dx.doi.org/10.1038/s41598-017-16795-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Su, Cathy
Gius, Jeffrey P.
Van Steenberg, Julia
Haskins, Alexis H.
Heishima, Kazuki
Omata, Chisato
Iwayama, Masahiro
Murakami, Mami
Mori, Takashi
Maruo, Kohji
Kato, Takamitsu A.
Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity
title Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity
title_full Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity
title_fullStr Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity
title_full_unstemmed Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity
title_short Hypersensitivity of BRCA2 deficient cells to rosemary extract explained by weak PARP inhibitory activity
title_sort hypersensitivity of brca2 deficient cells to rosemary extract explained by weak parp inhibitory activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711971/
https://www.ncbi.nlm.nih.gov/pubmed/29196727
http://dx.doi.org/10.1038/s41598-017-16795-3
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