Cargando…
Targeting neddylation E2s: a novel therapeutic strategy in cancer
Ubiquitin-conjugating enzyme E2 M (UBE2M) and ubiquitin-conjugating enzyme E2 F (UBE2F) are the two NEDD8-conjugating enzymes of the neddylation pathway that take part in posttranslational modification and change the activity of target proteins. The activity of E2 enzymes requires both a 26-residue...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028724/ https://www.ncbi.nlm.nih.gov/pubmed/33827629 http://dx.doi.org/10.1186/s13045-021-01070-w |
_version_ | 1783675993428328448 |
---|---|
author | Zheng, Yi-Chao Guo, Yan-Jia Wang, Bo Wang, Chong Mamun, M. A. A. Gao, Ya Liu, Hong-Min |
author_facet | Zheng, Yi-Chao Guo, Yan-Jia Wang, Bo Wang, Chong Mamun, M. A. A. Gao, Ya Liu, Hong-Min |
author_sort | Zheng, Yi-Chao |
collection | PubMed |
description | Ubiquitin-conjugating enzyme E2 M (UBE2M) and ubiquitin-conjugating enzyme E2 F (UBE2F) are the two NEDD8-conjugating enzymes of the neddylation pathway that take part in posttranslational modification and change the activity of target proteins. The activity of E2 enzymes requires both a 26-residue N-terminal docking peptide and a conserved E2 catalytic core domain, which is the basis for the transfer of neural precursor cell-expressed developmentally downregulated 8 (NEDD8). By recruiting E3 ligases and targeting cullin and non-cullin substrates, UBE2M and UBE2F play diverse biological roles. Currently, there are several inhibitors that target the UBE2M-defective in cullin neddylation protein 1 (DCN1) interaction to treat cancer. As described above, this review provides insights into the mechanism of UBE2M and UBE2F and emphasizes these two E2 enzymes as appealing therapeutic targets for the treatment of cancers. |
format | Online Article Text |
id | pubmed-8028724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80287242021-04-08 Targeting neddylation E2s: a novel therapeutic strategy in cancer Zheng, Yi-Chao Guo, Yan-Jia Wang, Bo Wang, Chong Mamun, M. A. A. Gao, Ya Liu, Hong-Min J Hematol Oncol Review Ubiquitin-conjugating enzyme E2 M (UBE2M) and ubiquitin-conjugating enzyme E2 F (UBE2F) are the two NEDD8-conjugating enzymes of the neddylation pathway that take part in posttranslational modification and change the activity of target proteins. The activity of E2 enzymes requires both a 26-residue N-terminal docking peptide and a conserved E2 catalytic core domain, which is the basis for the transfer of neural precursor cell-expressed developmentally downregulated 8 (NEDD8). By recruiting E3 ligases and targeting cullin and non-cullin substrates, UBE2M and UBE2F play diverse biological roles. Currently, there are several inhibitors that target the UBE2M-defective in cullin neddylation protein 1 (DCN1) interaction to treat cancer. As described above, this review provides insights into the mechanism of UBE2M and UBE2F and emphasizes these two E2 enzymes as appealing therapeutic targets for the treatment of cancers. BioMed Central 2021-04-07 /pmc/articles/PMC8028724/ /pubmed/33827629 http://dx.doi.org/10.1186/s13045-021-01070-w 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 Zheng, Yi-Chao Guo, Yan-Jia Wang, Bo Wang, Chong Mamun, M. A. A. Gao, Ya Liu, Hong-Min Targeting neddylation E2s: a novel therapeutic strategy in cancer |
title | Targeting neddylation E2s: a novel therapeutic strategy in cancer |
title_full | Targeting neddylation E2s: a novel therapeutic strategy in cancer |
title_fullStr | Targeting neddylation E2s: a novel therapeutic strategy in cancer |
title_full_unstemmed | Targeting neddylation E2s: a novel therapeutic strategy in cancer |
title_short | Targeting neddylation E2s: a novel therapeutic strategy in cancer |
title_sort | targeting neddylation e2s: a novel therapeutic strategy in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028724/ https://www.ncbi.nlm.nih.gov/pubmed/33827629 http://dx.doi.org/10.1186/s13045-021-01070-w |
work_keys_str_mv | AT zhengyichao targetingneddylatione2sanoveltherapeuticstrategyincancer AT guoyanjia targetingneddylatione2sanoveltherapeuticstrategyincancer AT wangbo targetingneddylatione2sanoveltherapeuticstrategyincancer AT wangchong targetingneddylatione2sanoveltherapeuticstrategyincancer AT mamunmaa targetingneddylatione2sanoveltherapeuticstrategyincancer AT gaoya targetingneddylatione2sanoveltherapeuticstrategyincancer AT liuhongmin targetingneddylatione2sanoveltherapeuticstrategyincancer |