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Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression

The notion that dietary antioxidants can help fight cancer is popular. However, the mechanism(s) behind the effect of antioxidants in cancer is still unclear. Previous studies indicate that supplements can influence gene expression; however, all of these studies were focused on the coding/exonic gen...

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Autores principales: Menon, Shreya, Lu, Chunxia, Menon, Rajasree, Schwartz, Jessica, Guan, Yuanfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4808750/
https://www.ncbi.nlm.nih.gov/pubmed/26805894
http://dx.doi.org/10.3390/antiox5010001
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author Menon, Shreya
Lu, Chunxia
Menon, Rajasree
Schwartz, Jessica
Guan, Yuanfang
author_facet Menon, Shreya
Lu, Chunxia
Menon, Rajasree
Schwartz, Jessica
Guan, Yuanfang
author_sort Menon, Shreya
collection PubMed
description The notion that dietary antioxidants can help fight cancer is popular. However, the mechanism(s) behind the effect of antioxidants in cancer is still unclear. Previous studies indicate that supplements can influence gene expression; however, all of these studies were focused on the coding/exonic gene expression. Studies are now emerging to highlight critical functional roles for RNAs expressed from the non-coding regions. This project was designed to study the effect of antioxidant supplements on non-coding intronic RNA expression in human cancers. Vitamin E, N-Acetyl cysteine (NAC) and Sulforaphane are commonly used supplements to prevent diseases including cancers. We studied the effect of these antioxidant supplements on the non-coding intronic RNA expression using publicly available datasets from a mouse model for lung cancer and prostate cancer cell lines. Although high throughput polyA-enriched RNA-Seq data characterize spliced coding mRNA regions, recent studies reveal the expression of reads from the non-coding intronic regions. Our analyses indicate that cancer cells have higher expression of introns compared to that of normal cells and that treatment with antioxidant supplements reduces the increased expression of introns of several genes. However, we did find high expression of introns of multiple genes including many oncogenes in the supplement treated groups compared to that of the control; this effect was distinct depending on the cell type and the supplement studied. Using RT-PCRs, we validated the expression of introns of two oncogenes, DLK1 and LRG1, known to be key players in lung cancer progression, and demonstrate changed intronic expression with supplement treatment in cancer cells. With regard to the antioxidant system, supplements did not change the intronic RNAs for endogenous antioxidant enzymes except for a significant decrease in the expression of superoxide dismutase (SOD) intronic RNA. Concurrently, we also found that a prolonged (48 h) exposure to Vitamin C, Vitamin E and Green tea extract reduced the enzymatic activity of SOD in lung cancer cells. The results from this study reveal that the antioxidant supplements have a significant effect on the intronic RNA expression of many genes including cancer genes that are not directly linked to the body’s antioxidant system. It is important to study this novel effect of antioxidant supplements in detail as it may have a significant role in disease progression.
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spelling pubmed-48087502016-04-04 Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression Menon, Shreya Lu, Chunxia Menon, Rajasree Schwartz, Jessica Guan, Yuanfang Antioxidants (Basel) Article The notion that dietary antioxidants can help fight cancer is popular. However, the mechanism(s) behind the effect of antioxidants in cancer is still unclear. Previous studies indicate that supplements can influence gene expression; however, all of these studies were focused on the coding/exonic gene expression. Studies are now emerging to highlight critical functional roles for RNAs expressed from the non-coding regions. This project was designed to study the effect of antioxidant supplements on non-coding intronic RNA expression in human cancers. Vitamin E, N-Acetyl cysteine (NAC) and Sulforaphane are commonly used supplements to prevent diseases including cancers. We studied the effect of these antioxidant supplements on the non-coding intronic RNA expression using publicly available datasets from a mouse model for lung cancer and prostate cancer cell lines. Although high throughput polyA-enriched RNA-Seq data characterize spliced coding mRNA regions, recent studies reveal the expression of reads from the non-coding intronic regions. Our analyses indicate that cancer cells have higher expression of introns compared to that of normal cells and that treatment with antioxidant supplements reduces the increased expression of introns of several genes. However, we did find high expression of introns of multiple genes including many oncogenes in the supplement treated groups compared to that of the control; this effect was distinct depending on the cell type and the supplement studied. Using RT-PCRs, we validated the expression of introns of two oncogenes, DLK1 and LRG1, known to be key players in lung cancer progression, and demonstrate changed intronic expression with supplement treatment in cancer cells. With regard to the antioxidant system, supplements did not change the intronic RNAs for endogenous antioxidant enzymes except for a significant decrease in the expression of superoxide dismutase (SOD) intronic RNA. Concurrently, we also found that a prolonged (48 h) exposure to Vitamin C, Vitamin E and Green tea extract reduced the enzymatic activity of SOD in lung cancer cells. The results from this study reveal that the antioxidant supplements have a significant effect on the intronic RNA expression of many genes including cancer genes that are not directly linked to the body’s antioxidant system. It is important to study this novel effect of antioxidant supplements in detail as it may have a significant role in disease progression. MDPI 2016-01-04 /pmc/articles/PMC4808750/ /pubmed/26805894 http://dx.doi.org/10.3390/antiox5010001 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Menon, Shreya
Lu, Chunxia
Menon, Rajasree
Schwartz, Jessica
Guan, Yuanfang
Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression
title Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression
title_full Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression
title_fullStr Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression
title_full_unstemmed Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression
title_short Effects of Antioxidants in Human Cancers: Differential Effects on Non-Coding Intronic RNA Expression
title_sort effects of antioxidants in human cancers: differential effects on non-coding intronic rna expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4808750/
https://www.ncbi.nlm.nih.gov/pubmed/26805894
http://dx.doi.org/10.3390/antiox5010001
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