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Decitabine: a historical review of the development of an epigenetic drug
The development of decitabine from its synthesis in 1964 to the submission of a registration file has been described. Although the unique DNA-demethylating capacity of decitabine is known for a long time, its application is under continuing investigation. The use of decitabine in MDS, AML, CML, stem...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103145/ https://www.ncbi.nlm.nih.gov/pubmed/16220311 http://dx.doi.org/10.1007/s00277-005-0008-x |
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author | de Vos, Dick van Overveld, Wendy |
author_facet | de Vos, Dick van Overveld, Wendy |
author_sort | de Vos, Dick |
collection | PubMed |
description | The development of decitabine from its synthesis in 1964 to the submission of a registration file has been described. Although the unique DNA-demethylating capacity of decitabine is known for a long time, its application is under continuing investigation. The use of decitabine in MDS, AML, CML, stem cell transplant, sickle cell anemia and thalassemia looks promising. The epigenetic dose seems lower than the cytotoxic dose. Whereas most drugs have matured after 40 years, decitabine is only at the beginning of a new development phase in epigenesis. |
format | Online Article Text |
id | pubmed-7103145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-71031452020-03-31 Decitabine: a historical review of the development of an epigenetic drug de Vos, Dick van Overveld, Wendy Ann Hematol Original Article The development of decitabine from its synthesis in 1964 to the submission of a registration file has been described. Although the unique DNA-demethylating capacity of decitabine is known for a long time, its application is under continuing investigation. The use of decitabine in MDS, AML, CML, stem cell transplant, sickle cell anemia and thalassemia looks promising. The epigenetic dose seems lower than the cytotoxic dose. Whereas most drugs have matured after 40 years, decitabine is only at the beginning of a new development phase in epigenesis. Springer-Verlag 2005-10-12 2005 /pmc/articles/PMC7103145/ /pubmed/16220311 http://dx.doi.org/10.1007/s00277-005-0008-x Text en © Springer-Verlag 2005 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article de Vos, Dick van Overveld, Wendy Decitabine: a historical review of the development of an epigenetic drug |
title | Decitabine: a historical review of the development of an epigenetic drug |
title_full | Decitabine: a historical review of the development of an epigenetic drug |
title_fullStr | Decitabine: a historical review of the development of an epigenetic drug |
title_full_unstemmed | Decitabine: a historical review of the development of an epigenetic drug |
title_short | Decitabine: a historical review of the development of an epigenetic drug |
title_sort | decitabine: a historical review of the development of an epigenetic drug |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103145/ https://www.ncbi.nlm.nih.gov/pubmed/16220311 http://dx.doi.org/10.1007/s00277-005-0008-x |
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