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Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends

Epigenetic drug discovery field has evidenced significant advancement in the recent times. A plethora of small molecule inhibitors have progressed to clinical stage investigations and are being explored exhaustively to ascertain conclusive benefits in diverse malignancies. Literature precedents indi...

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Autores principales: Nepali, Kunal, Liou, Jing-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040241/
https://www.ncbi.nlm.nih.gov/pubmed/33840388
http://dx.doi.org/10.1186/s12929-021-00721-x
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author Nepali, Kunal
Liou, Jing-Ping
author_facet Nepali, Kunal
Liou, Jing-Ping
author_sort Nepali, Kunal
collection PubMed
description Epigenetic drug discovery field has evidenced significant advancement in the recent times. A plethora of small molecule inhibitors have progressed to clinical stage investigations and are being explored exhaustively to ascertain conclusive benefits in diverse malignancies. Literature precedents indicates that substantial amount of efforts were directed towards the use of epigenetic tools in monotherapy as well as in combination regimens at the clinical level, however, the preclinical/preliminary explorations were inclined towards the identification of prudent approaches that can leverage the anticancer potential of small molecule epigenetic inhibitors as single agents only. This review article presents an update of FDA approved epigenetic drugs along with the epigenetic inhibitors undergoing clinical stage investigations in different cancer types. A detailed discussion of the pragmatic strategies that are expected to steer the progress of the epigenetic therapy through the implementation of emerging approaches such as PROTACS and CRISPR/Cas9 along with logical ways for scaffold fabrication to selectively approach the enzyme isoforms in pursuit of garnering amplified antitumor effects has been covered. In addition, the compilation also presents the rational strategies for the construction of multi-targeting scaffold assemblages employing previously identified pharmacophores as potential alternatives to the combination therapy.
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spelling pubmed-80402412021-04-12 Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends Nepali, Kunal Liou, Jing-Ping J Biomed Sci Review Epigenetic drug discovery field has evidenced significant advancement in the recent times. A plethora of small molecule inhibitors have progressed to clinical stage investigations and are being explored exhaustively to ascertain conclusive benefits in diverse malignancies. Literature precedents indicates that substantial amount of efforts were directed towards the use of epigenetic tools in monotherapy as well as in combination regimens at the clinical level, however, the preclinical/preliminary explorations were inclined towards the identification of prudent approaches that can leverage the anticancer potential of small molecule epigenetic inhibitors as single agents only. This review article presents an update of FDA approved epigenetic drugs along with the epigenetic inhibitors undergoing clinical stage investigations in different cancer types. A detailed discussion of the pragmatic strategies that are expected to steer the progress of the epigenetic therapy through the implementation of emerging approaches such as PROTACS and CRISPR/Cas9 along with logical ways for scaffold fabrication to selectively approach the enzyme isoforms in pursuit of garnering amplified antitumor effects has been covered. In addition, the compilation also presents the rational strategies for the construction of multi-targeting scaffold assemblages employing previously identified pharmacophores as potential alternatives to the combination therapy. BioMed Central 2021-04-12 /pmc/articles/PMC8040241/ /pubmed/33840388 http://dx.doi.org/10.1186/s12929-021-00721-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Nepali, Kunal
Liou, Jing-Ping
Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends
title Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends
title_full Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends
title_fullStr Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends
title_full_unstemmed Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends
title_short Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends
title_sort recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040241/
https://www.ncbi.nlm.nih.gov/pubmed/33840388
http://dx.doi.org/10.1186/s12929-021-00721-x
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