Cargando…

Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications

Previously, we and others have shown that the regular intake of green tea polyphenols (GTPs) reduces ultraviolet B (UVB) radiation-induced skin cancer by targeting multiple signaling pathways, including DNA damage, DNA repair, immunosuppression, and inflammation. Here, we determine the effect of GTP...

Descripción completa

Detalles Bibliográficos
Autores principales: Kansal, Vikash, Agarwal, Anshu, Harbour, Angela, Farooqi, Humaira, Singh, Vijay Kumar, Prasad, Ram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777720/
https://www.ncbi.nlm.nih.gov/pubmed/35054091
http://dx.doi.org/10.3390/jcm11020398
_version_ 1784637134672494592
author Kansal, Vikash
Agarwal, Anshu
Harbour, Angela
Farooqi, Humaira
Singh, Vijay Kumar
Prasad, Ram
author_facet Kansal, Vikash
Agarwal, Anshu
Harbour, Angela
Farooqi, Humaira
Singh, Vijay Kumar
Prasad, Ram
author_sort Kansal, Vikash
collection PubMed
description Previously, we and others have shown that the regular intake of green tea polyphenols (GTPs) reduces ultraviolet B (UVB) radiation-induced skin cancer by targeting multiple signaling pathways, including DNA damage, DNA repair, immunosuppression, and inflammation. Here, we determine the effect of GTPs on UVB-induced epigenetic changes, emphasizing DNA hypermethylation in UV-exposed skin and tumors and their association with miR-29, a key regulator of DNA methyltransferases (DNMTs). Skin cancer was induced in SKH-1 hairless mice following repeated exposures of UVB radiation (180 mJ/cm(2), three times/week, 24 weeks) with or without GTPs supplementation (0.2%) in drinking water. Regular intake of GTPs inhibited tumor growth by hindering the cascade of DNA hypermethylation events. GTPs supplementation significantly blocked UVB-induced DNA hypermethylation in the skin (up to 35%; p < 0.0001) and in tumors (up to 50%; p < 0.0001). Experimental results showed that the levels of DNA hypermethylation were higher in GTPs-treated mice than in the control group. The expressions of miR-29a, miR-29b, and miR-29c were markedly decreased in UV-induced skin tumors, and GTPs administration blocked UVB-induced miR-29s depletion. Furthermore, these observations were verified using the in vitro approach in human skin cancer cells (A431) followed by treatment with GTPs or mimics of miR-29c. Increased levels of miR-29 were observed in GTPs-treated A431 cells, resulting in increased TET activity and decreased DNA hypermethylation. In conclusion, UVB-mediated miR-29 depletion promotes DNA hypermethylation and leads to enhanced tumor growth by silencing tumor suppressors. Regular intake of GTPs rescued UVB-induced miR-29 depletion and prevented tumor growth by maintaining reduced DNA hypermethylation and activating tumor suppressors. Our observations suggest that miR-based strategies and regular consumption of GTPs could minimize the risk of UVB-induced skin cancers and contribute to better management of NMSCs.
format Online
Article
Text
id pubmed-8777720
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-87777202022-01-22 Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications Kansal, Vikash Agarwal, Anshu Harbour, Angela Farooqi, Humaira Singh, Vijay Kumar Prasad, Ram J Clin Med Article Previously, we and others have shown that the regular intake of green tea polyphenols (GTPs) reduces ultraviolet B (UVB) radiation-induced skin cancer by targeting multiple signaling pathways, including DNA damage, DNA repair, immunosuppression, and inflammation. Here, we determine the effect of GTPs on UVB-induced epigenetic changes, emphasizing DNA hypermethylation in UV-exposed skin and tumors and their association with miR-29, a key regulator of DNA methyltransferases (DNMTs). Skin cancer was induced in SKH-1 hairless mice following repeated exposures of UVB radiation (180 mJ/cm(2), three times/week, 24 weeks) with or without GTPs supplementation (0.2%) in drinking water. Regular intake of GTPs inhibited tumor growth by hindering the cascade of DNA hypermethylation events. GTPs supplementation significantly blocked UVB-induced DNA hypermethylation in the skin (up to 35%; p < 0.0001) and in tumors (up to 50%; p < 0.0001). Experimental results showed that the levels of DNA hypermethylation were higher in GTPs-treated mice than in the control group. The expressions of miR-29a, miR-29b, and miR-29c were markedly decreased in UV-induced skin tumors, and GTPs administration blocked UVB-induced miR-29s depletion. Furthermore, these observations were verified using the in vitro approach in human skin cancer cells (A431) followed by treatment with GTPs or mimics of miR-29c. Increased levels of miR-29 were observed in GTPs-treated A431 cells, resulting in increased TET activity and decreased DNA hypermethylation. In conclusion, UVB-mediated miR-29 depletion promotes DNA hypermethylation and leads to enhanced tumor growth by silencing tumor suppressors. Regular intake of GTPs rescued UVB-induced miR-29 depletion and prevented tumor growth by maintaining reduced DNA hypermethylation and activating tumor suppressors. Our observations suggest that miR-based strategies and regular consumption of GTPs could minimize the risk of UVB-induced skin cancers and contribute to better management of NMSCs. MDPI 2022-01-13 /pmc/articles/PMC8777720/ /pubmed/35054091 http://dx.doi.org/10.3390/jcm11020398 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
Kansal, Vikash
Agarwal, Anshu
Harbour, Angela
Farooqi, Humaira
Singh, Vijay Kumar
Prasad, Ram
Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications
title Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications
title_full Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications
title_fullStr Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications
title_full_unstemmed Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications
title_short Regular Intake of Green Tea Polyphenols Suppresses the Development of Nonmelanoma Skin Cancer through miR-29-Mediated Epigenetic Modifications
title_sort regular intake of green tea polyphenols suppresses the development of nonmelanoma skin cancer through mir-29-mediated epigenetic modifications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777720/
https://www.ncbi.nlm.nih.gov/pubmed/35054091
http://dx.doi.org/10.3390/jcm11020398
work_keys_str_mv AT kansalvikash regularintakeofgreenteapolyphenolssuppressesthedevelopmentofnonmelanomaskincancerthroughmir29mediatedepigeneticmodifications
AT agarwalanshu regularintakeofgreenteapolyphenolssuppressesthedevelopmentofnonmelanomaskincancerthroughmir29mediatedepigeneticmodifications
AT harbourangela regularintakeofgreenteapolyphenolssuppressesthedevelopmentofnonmelanomaskincancerthroughmir29mediatedepigeneticmodifications
AT farooqihumaira regularintakeofgreenteapolyphenolssuppressesthedevelopmentofnonmelanomaskincancerthroughmir29mediatedepigeneticmodifications
AT singhvijaykumar regularintakeofgreenteapolyphenolssuppressesthedevelopmentofnonmelanomaskincancerthroughmir29mediatedepigeneticmodifications
AT prasadram regularintakeofgreenteapolyphenolssuppressesthedevelopmentofnonmelanomaskincancerthroughmir29mediatedepigeneticmodifications