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Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers
The bromodomain and extraterminal (BET) domain protein family is involved in the process of transcription of genetic information. The BET protein family includes BRD2, BRD3, BRD4, and bromodomain testis-specific protein. BET protein alterations are associated with some solid tumor cancers, including...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208386/ https://www.ncbi.nlm.nih.gov/pubmed/35756176 http://dx.doi.org/10.4103/JIPO.JIPO_2_20 |
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author | Nguyen, Martin V. Loof, Lydia Falchook, Gerald S. |
author_facet | Nguyen, Martin V. Loof, Lydia Falchook, Gerald S. |
author_sort | Nguyen, Martin V. |
collection | PubMed |
description | The bromodomain and extraterminal (BET) domain protein family is involved in the process of transcription of genetic information. The BET protein family includes BRD2, BRD3, BRD4, and bromodomain testis-specific protein. BET protein alterations are associated with some solid tumor cancers, including nuclear protein in testis midline carcinoma. BET protein has a role in carcinogenesis and in the regulation of the cell cycle. A number of BET inhibitors have entered clinical trials. This review discusses the results of BET inhibitor clinical trials in solid tumor cancers. |
format | Online Article Text |
id | pubmed-9208386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-92083862022-06-23 Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers Nguyen, Martin V. Loof, Lydia Falchook, Gerald S. J Immunother Precis Oncol Review Articles The bromodomain and extraterminal (BET) domain protein family is involved in the process of transcription of genetic information. The BET protein family includes BRD2, BRD3, BRD4, and bromodomain testis-specific protein. BET protein alterations are associated with some solid tumor cancers, including nuclear protein in testis midline carcinoma. BET protein has a role in carcinogenesis and in the regulation of the cell cycle. A number of BET inhibitors have entered clinical trials. This review discusses the results of BET inhibitor clinical trials in solid tumor cancers. Wolters Kluwer - Medknow 2020-02-05 /pmc/articles/PMC9208386/ /pubmed/35756176 http://dx.doi.org/10.4103/JIPO.JIPO_2_20 Text en © 2020 Journal of Immunotherapy and Precision Oncology | Published by Wolters Kluwer - Medknow https://creativecommons.org/licenses/by/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License (https://creativecommons.org/licenses/by/4.0/) , which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Articles Nguyen, Martin V. Loof, Lydia Falchook, Gerald S. Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers |
title | Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers |
title_full | Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers |
title_fullStr | Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers |
title_full_unstemmed | Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers |
title_short | Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers |
title_sort | bromodomain and extra-terminal (bet) domain protein inhibitors for solid tumor cancers |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208386/ https://www.ncbi.nlm.nih.gov/pubmed/35756176 http://dx.doi.org/10.4103/JIPO.JIPO_2_20 |
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