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Detection and manipulation of methylation in blood cancer DNA using terahertz radiation
DNA methylation is a pivotal epigenetic modification of DNA that regulates gene expression. Abnormal regulation of gene expression is closely related to carcinogenesis, which is why the assessment of DNA methylation is a key factor in cancer research. Terahertz radiation may play an important role i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478716/ https://www.ncbi.nlm.nih.gov/pubmed/31015556 http://dx.doi.org/10.1038/s41598-019-42855-x |
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author | Cheon, Hwayeong Paik, Jin Ho Choi, Moran Yang, Hee-Jin Son, Joo-Hiuk |
author_facet | Cheon, Hwayeong Paik, Jin Ho Choi, Moran Yang, Hee-Jin Son, Joo-Hiuk |
author_sort | Cheon, Hwayeong |
collection | PubMed |
description | DNA methylation is a pivotal epigenetic modification of DNA that regulates gene expression. Abnormal regulation of gene expression is closely related to carcinogenesis, which is why the assessment of DNA methylation is a key factor in cancer research. Terahertz radiation may play an important role in active demethylation for cancer therapy because the characteristic frequency of the methylated DNA exists in the terahertz region. Here, we present a novel technique for the detection and manipulation of DNA methylation using terahertz radiation in blood cancer cell lines. We observed the degree of DNA methylation in blood cancer at the characteristic resonance of approximately 1.7 THz using terahertz time-domain spectroscopy. The terahertz results were cross-checked with global DNA methylation quantification using an enzyme-linked immunosorbent assay. We also achieved the demethylation of cancer DNA using high-power terahertz radiation at the 1.7-THz resonance. The demethylation degrees ranged from 10% to 70%, depending on the type of cancer cell line. Our results show the detection of DNA methylation based on the terahertz molecular resonance and the manipulation of global DNA methylation using high-power terahertz radiation. Terahertz radiation may have potential applications as an epigenetic inhibitor in cancer treatment, by virtue of its ability to induce DNA demethylation, similarly to decitabine. |
format | Online Article Text |
id | pubmed-6478716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64787162019-05-03 Detection and manipulation of methylation in blood cancer DNA using terahertz radiation Cheon, Hwayeong Paik, Jin Ho Choi, Moran Yang, Hee-Jin Son, Joo-Hiuk Sci Rep Article DNA methylation is a pivotal epigenetic modification of DNA that regulates gene expression. Abnormal regulation of gene expression is closely related to carcinogenesis, which is why the assessment of DNA methylation is a key factor in cancer research. Terahertz radiation may play an important role in active demethylation for cancer therapy because the characteristic frequency of the methylated DNA exists in the terahertz region. Here, we present a novel technique for the detection and manipulation of DNA methylation using terahertz radiation in blood cancer cell lines. We observed the degree of DNA methylation in blood cancer at the characteristic resonance of approximately 1.7 THz using terahertz time-domain spectroscopy. The terahertz results were cross-checked with global DNA methylation quantification using an enzyme-linked immunosorbent assay. We also achieved the demethylation of cancer DNA using high-power terahertz radiation at the 1.7-THz resonance. The demethylation degrees ranged from 10% to 70%, depending on the type of cancer cell line. Our results show the detection of DNA methylation based on the terahertz molecular resonance and the manipulation of global DNA methylation using high-power terahertz radiation. Terahertz radiation may have potential applications as an epigenetic inhibitor in cancer treatment, by virtue of its ability to induce DNA demethylation, similarly to decitabine. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478716/ /pubmed/31015556 http://dx.doi.org/10.1038/s41598-019-42855-x Text en © The Author(s) 2019 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 Cheon, Hwayeong Paik, Jin Ho Choi, Moran Yang, Hee-Jin Son, Joo-Hiuk Detection and manipulation of methylation in blood cancer DNA using terahertz radiation |
title | Detection and manipulation of methylation in blood cancer DNA using terahertz radiation |
title_full | Detection and manipulation of methylation in blood cancer DNA using terahertz radiation |
title_fullStr | Detection and manipulation of methylation in blood cancer DNA using terahertz radiation |
title_full_unstemmed | Detection and manipulation of methylation in blood cancer DNA using terahertz radiation |
title_short | Detection and manipulation of methylation in blood cancer DNA using terahertz radiation |
title_sort | detection and manipulation of methylation in blood cancer dna using terahertz radiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478716/ https://www.ncbi.nlm.nih.gov/pubmed/31015556 http://dx.doi.org/10.1038/s41598-019-42855-x |
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