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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2019
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.
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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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