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Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer
Methylation is a primary epigenetic mechanism regulating gene expression. 5-aza-2′-deoxycytidine is an FDA-approved drug prescribed for treatment of cancer by inhibiting DNA-Methyl-Transferase 1 (DNMT1). Results of this study suggest that prolonged treatment with 5-aza-2′-deoxycytidine could induce...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549914/ https://www.ncbi.nlm.nih.gov/pubmed/31068247 http://dx.doi.org/10.5483/BMBRep.2019.52.5.055 |
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author | Kim, Dong Hyun Kim, Hye-Min Huong, Pham Thi Thu Han, Ho-Jin Hwang, Joonsung Cha-Molstad, Hyunjoo Lee, Kyung Ho Ryoo, In-Ja Kim, Kyoon Eon Huh, Yang Hoon Ahn, Jong Seog Kwon, Yong Tae Soung, Nak-Kyun Kim, Bo Yeon |
author_facet | Kim, Dong Hyun Kim, Hye-Min Huong, Pham Thi Thu Han, Ho-Jin Hwang, Joonsung Cha-Molstad, Hyunjoo Lee, Kyung Ho Ryoo, In-Ja Kim, Kyoon Eon Huh, Yang Hoon Ahn, Jong Seog Kwon, Yong Tae Soung, Nak-Kyun Kim, Bo Yeon |
author_sort | Kim, Dong Hyun |
collection | PubMed |
description | Methylation is a primary epigenetic mechanism regulating gene expression. 5-aza-2′-deoxycytidine is an FDA-approved drug prescribed for treatment of cancer by inhibiting DNA-Methyl-Transferase 1 (DNMT1). Results of this study suggest that prolonged treatment with 5-aza-2′-deoxycytidine could induce centrosome abnormalities in cancer cells and that CEP131, a centrosome protein, is regulated by DNMT1. Interestingly, cancer cell growth was attenuated in vitro and in vivo by inhibiting the expression of Cep131. Finally, Cep131-deficient cells were more sensitive to treatment with DNMT1 inhibitors. These findings suggest that Cep131 is a potential novel anti-cancer target. Agents that can inhibit this protein may be useful alone or in combination with DNMT1 inhibitors to treat cancer. |
format | Online Article Text |
id | pubmed-6549914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65499142019-06-19 Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer Kim, Dong Hyun Kim, Hye-Min Huong, Pham Thi Thu Han, Ho-Jin Hwang, Joonsung Cha-Molstad, Hyunjoo Lee, Kyung Ho Ryoo, In-Ja Kim, Kyoon Eon Huh, Yang Hoon Ahn, Jong Seog Kwon, Yong Tae Soung, Nak-Kyun Kim, Bo Yeon BMB Rep Articles Methylation is a primary epigenetic mechanism regulating gene expression. 5-aza-2′-deoxycytidine is an FDA-approved drug prescribed for treatment of cancer by inhibiting DNA-Methyl-Transferase 1 (DNMT1). Results of this study suggest that prolonged treatment with 5-aza-2′-deoxycytidine could induce centrosome abnormalities in cancer cells and that CEP131, a centrosome protein, is regulated by DNMT1. Interestingly, cancer cell growth was attenuated in vitro and in vivo by inhibiting the expression of Cep131. Finally, Cep131-deficient cells were more sensitive to treatment with DNMT1 inhibitors. These findings suggest that Cep131 is a potential novel anti-cancer target. Agents that can inhibit this protein may be useful alone or in combination with DNMT1 inhibitors to treat cancer. Korean Society for Biochemistry and Molecular Biology 2019-05 2019-05-31 /pmc/articles/PMC6549914/ /pubmed/31068247 http://dx.doi.org/10.5483/BMBRep.2019.52.5.055 Text en Copyright © 2019 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Kim, Dong Hyun Kim, Hye-Min Huong, Pham Thi Thu Han, Ho-Jin Hwang, Joonsung Cha-Molstad, Hyunjoo Lee, Kyung Ho Ryoo, In-Ja Kim, Kyoon Eon Huh, Yang Hoon Ahn, Jong Seog Kwon, Yong Tae Soung, Nak-Kyun Kim, Bo Yeon Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer |
title | Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer |
title_full | Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer |
title_fullStr | Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer |
title_full_unstemmed | Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer |
title_short | Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer |
title_sort | enhanced anticancer effects of a methylation inhibitor by inhibiting a novel dnmt1 target, cep 131, in cervical cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549914/ https://www.ncbi.nlm.nih.gov/pubmed/31068247 http://dx.doi.org/10.5483/BMBRep.2019.52.5.055 |
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