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Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells

We previously reported that oral administration of black raspberry powder decreased promoter methylation of tumor suppressor genes in tumors from patients with colorectal cancer. The anthocyanins (ACs) in black raspberries are responsible, at least in part, for their cancer-inhibitory effects. In th...

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Autores principales: Wang, Li-Shu, Kuo, Chieh-Ti, Cho, Seung-Ju, Seguin, Claire, Siddiqui, Jibran, Stoner, Kristen, Weng, Yu-I, Huang, Tim H.-M., Tichelaar, Jay, Yearsley, Martha, Stoner, Gary D., Huang, Yi-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570951/
https://www.ncbi.nlm.nih.gov/pubmed/23368921
http://dx.doi.org/10.1080/01635581.2013.741759
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author Wang, Li-Shu
Kuo, Chieh-Ti
Cho, Seung-Ju
Seguin, Claire
Siddiqui, Jibran
Stoner, Kristen
Weng, Yu-I
Huang, Tim H.-M.
Tichelaar, Jay
Yearsley, Martha
Stoner, Gary D.
Huang, Yi-Wen
author_facet Wang, Li-Shu
Kuo, Chieh-Ti
Cho, Seung-Ju
Seguin, Claire
Siddiqui, Jibran
Stoner, Kristen
Weng, Yu-I
Huang, Tim H.-M.
Tichelaar, Jay
Yearsley, Martha
Stoner, Gary D.
Huang, Yi-Wen
author_sort Wang, Li-Shu
collection PubMed
description We previously reported that oral administration of black raspberry powder decreased promoter methylation of tumor suppressor genes in tumors from patients with colorectal cancer. The anthocyanins (ACs) in black raspberries are responsible, at least in part, for their cancer-inhibitory effects. In the present study, we asked if ACs are responsible for the demethylation effects observed in colorectal cancers. Three days of treatment of ACs at 0.5, 5, and 25 μg/ml suppressed activity and protein expression of DNMT1 and DNMT3B in HCT116, Caco2 and SW480 cells. Promoters of CDKN2A, and SFRP2, SFRP5, and WIF1, upstream of Wnt pathway, were demethylated by ACs. mRNA expression of some of these genes was increased. mRNA expression of β-catenin and c-Myc, downstream of Wnt pathway, and cell proliferation were decreased; apoptosis was increased. ACs were taken up into HCT116 cells and were differentially localized with DNMT1 and DNMT3B in the same cells visualized using confocal laser scanning microscopy. Although it was reported that DNMT3B is regulated by c-Myc in mouse lymphoma, DNMT3B did not bind with c-Myc in HCT116 cells. In conclusion, our results suggest that ACs are responsible, at least in part, for the demethylation effects of whole black raspberries in colorectal cancers.
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spelling pubmed-35709512013-02-15 Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells Wang, Li-Shu Kuo, Chieh-Ti Cho, Seung-Ju Seguin, Claire Siddiqui, Jibran Stoner, Kristen Weng, Yu-I Huang, Tim H.-M. Tichelaar, Jay Yearsley, Martha Stoner, Gary D. Huang, Yi-Wen Nutr Cancer Research Article We previously reported that oral administration of black raspberry powder decreased promoter methylation of tumor suppressor genes in tumors from patients with colorectal cancer. The anthocyanins (ACs) in black raspberries are responsible, at least in part, for their cancer-inhibitory effects. In the present study, we asked if ACs are responsible for the demethylation effects observed in colorectal cancers. Three days of treatment of ACs at 0.5, 5, and 25 μg/ml suppressed activity and protein expression of DNMT1 and DNMT3B in HCT116, Caco2 and SW480 cells. Promoters of CDKN2A, and SFRP2, SFRP5, and WIF1, upstream of Wnt pathway, were demethylated by ACs. mRNA expression of some of these genes was increased. mRNA expression of β-catenin and c-Myc, downstream of Wnt pathway, and cell proliferation were decreased; apoptosis was increased. ACs were taken up into HCT116 cells and were differentially localized with DNMT1 and DNMT3B in the same cells visualized using confocal laser scanning microscopy. Although it was reported that DNMT3B is regulated by c-Myc in mouse lymphoma, DNMT3B did not bind with c-Myc in HCT116 cells. In conclusion, our results suggest that ACs are responsible, at least in part, for the demethylation effects of whole black raspberries in colorectal cancers. Taylor & Francis 2013-01-31 2013-01 /pmc/articles/PMC3570951/ /pubmed/23368921 http://dx.doi.org/10.1080/01635581.2013.741759 Text en Copyright © 2013, Taylor & Francis Group, LLC http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Taylor & Francis journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Li-Shu
Kuo, Chieh-Ti
Cho, Seung-Ju
Seguin, Claire
Siddiqui, Jibran
Stoner, Kristen
Weng, Yu-I
Huang, Tim H.-M.
Tichelaar, Jay
Yearsley, Martha
Stoner, Gary D.
Huang, Yi-Wen
Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells
title Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells
title_full Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells
title_fullStr Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells
title_full_unstemmed Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells
title_short Black Raspberry-Derived Anthocyanins Demethylate Tumor Suppressor Genes Through the Inhibition of DNMT1 and DNMT3B in Colon Cancer Cells
title_sort black raspberry-derived anthocyanins demethylate tumor suppressor genes through the inhibition of dnmt1 and dnmt3b in colon cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570951/
https://www.ncbi.nlm.nih.gov/pubmed/23368921
http://dx.doi.org/10.1080/01635581.2013.741759
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