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AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines

Novel and effective chemotherapeutic agents are needed to improve cancer treatment. Epidrugs are currently used for cancer therapy but also exhibit toxicity. Targeting the epigenetic apparatus with bioproducts may aid cancer prevention and treatment. To determine whether the lipoprotein marine extra...

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Autores principales: Martínez-Iglesias, Olaia, Carrera, Ivan, Naidoo, Vinogran, Cacabelos, Ramón
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780983/
https://www.ncbi.nlm.nih.gov/pubmed/35054489
http://dx.doi.org/10.3390/life12010097
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author Martínez-Iglesias, Olaia
Carrera, Ivan
Naidoo, Vinogran
Cacabelos, Ramón
author_facet Martínez-Iglesias, Olaia
Carrera, Ivan
Naidoo, Vinogran
Cacabelos, Ramón
author_sort Martínez-Iglesias, Olaia
collection PubMed
description Novel and effective chemotherapeutic agents are needed to improve cancer treatment. Epidrugs are currently used for cancer therapy but also exhibit toxicity. Targeting the epigenetic apparatus with bioproducts may aid cancer prevention and treatment. To determine whether the lipoprotein marine extract AntiGan shows epigenetic and antitumor effects, cultured HepG2 (hepatocellular carcinoma) and HCT116 (colorectal carcinoma) cell lines were treated with AntiGan (10, 50, 100, and to 500 µg/mL) for 24 h, 48 h, and 72 h. AntiGan (10 µg/mL) reduced cell viability after 48 h and increased Bax expression; AntiGan (10 and 50 µg/mL) increased caspase-3 immunoreactivity in HepG2 and HCT116 cells. AntiGan (10 and 50 µg/mL) attenuated COX-2 and IL-17 expression in both cell lines. AntiGan (10 µg/mL) increased 5mC levels in both cell types and reduced DNMT1 and DNMT3a expression in these cells. AntiGan (10 and 50 µg/mL) promoted DNMT3a immunoreactivity and reduced SIRT1 mRNA expression in both cell types. In HCT116 cells treated with AntiGan (10 µg/mL), SIRT1 immunoreactivity localized to nuclei and the cytoplasm; AntiGan (50 µg/mL) increased cytoplasmic SIRT1 localization in HCT116 cells. AntiGan is a novel antitumoral bioproduct with epigenetic properties (epinutraceutical) for treating liver and colorectal cancer.
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spelling pubmed-87809832022-01-22 AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines Martínez-Iglesias, Olaia Carrera, Ivan Naidoo, Vinogran Cacabelos, Ramón Life (Basel) Article Novel and effective chemotherapeutic agents are needed to improve cancer treatment. Epidrugs are currently used for cancer therapy but also exhibit toxicity. Targeting the epigenetic apparatus with bioproducts may aid cancer prevention and treatment. To determine whether the lipoprotein marine extract AntiGan shows epigenetic and antitumor effects, cultured HepG2 (hepatocellular carcinoma) and HCT116 (colorectal carcinoma) cell lines were treated with AntiGan (10, 50, 100, and to 500 µg/mL) for 24 h, 48 h, and 72 h. AntiGan (10 µg/mL) reduced cell viability after 48 h and increased Bax expression; AntiGan (10 and 50 µg/mL) increased caspase-3 immunoreactivity in HepG2 and HCT116 cells. AntiGan (10 and 50 µg/mL) attenuated COX-2 and IL-17 expression in both cell lines. AntiGan (10 µg/mL) increased 5mC levels in both cell types and reduced DNMT1 and DNMT3a expression in these cells. AntiGan (10 and 50 µg/mL) promoted DNMT3a immunoreactivity and reduced SIRT1 mRNA expression in both cell types. In HCT116 cells treated with AntiGan (10 µg/mL), SIRT1 immunoreactivity localized to nuclei and the cytoplasm; AntiGan (50 µg/mL) increased cytoplasmic SIRT1 localization in HCT116 cells. AntiGan is a novel antitumoral bioproduct with epigenetic properties (epinutraceutical) for treating liver and colorectal cancer. MDPI 2022-01-10 /pmc/articles/PMC8780983/ /pubmed/35054489 http://dx.doi.org/10.3390/life12010097 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
Martínez-Iglesias, Olaia
Carrera, Ivan
Naidoo, Vinogran
Cacabelos, Ramón
AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines
title AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines
title_full AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines
title_fullStr AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines
title_full_unstemmed AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines
title_short AntiGan: An Epinutraceutical Bioproduct with Antitumor Properties in Cultured Cell Lines
title_sort antigan: an epinutraceutical bioproduct with antitumor properties in cultured cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780983/
https://www.ncbi.nlm.nih.gov/pubmed/35054489
http://dx.doi.org/10.3390/life12010097
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