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Reverse the Resistance to PARP Inhibitors
One of the DNA repair machineries is activated by Poly (ADP-ribose) Polymerase (PARP) enzyme. Particularly, this enzyme is involved in repair of damages to single-strand DNA, thus decreasing the chances of generating double-strand breaks in the genome. Therefore, the concept to block PARP enzymes by...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332874/ https://www.ncbi.nlm.nih.gov/pubmed/28255272 http://dx.doi.org/10.7150/ijbs.17240 |
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author | Kim, Yevgeniy Kim, Aleksei Sharip, Ainur Sharip, Aigul Jiang, Juhong Yang, Qing Xie, Yingqiu |
author_facet | Kim, Yevgeniy Kim, Aleksei Sharip, Ainur Sharip, Aigul Jiang, Juhong Yang, Qing Xie, Yingqiu |
author_sort | Kim, Yevgeniy |
collection | PubMed |
description | One of the DNA repair machineries is activated by Poly (ADP-ribose) Polymerase (PARP) enzyme. Particularly, this enzyme is involved in repair of damages to single-strand DNA, thus decreasing the chances of generating double-strand breaks in the genome. Therefore, the concept to block PARP enzymes by PARP inhibitor (PARPi) was appreciated in cancer treatment. PARPi has been designed and tested for many years and became a potential supplement for the conventional chemotherapy. However, increasing evidence indicates the appearance of the resistance to this treatment. Specifically, cancer cells may acquire new mutations or events that overcome the positive effect of these drugs. This paper describes several molecular mechanisms of PARPi resistance which were reported most recently, and summarizes some strategies to reverse this type of drug resistance. |
format | Online Article Text |
id | pubmed-5332874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-53328742017-03-02 Reverse the Resistance to PARP Inhibitors Kim, Yevgeniy Kim, Aleksei Sharip, Ainur Sharip, Aigul Jiang, Juhong Yang, Qing Xie, Yingqiu Int J Biol Sci Review One of the DNA repair machineries is activated by Poly (ADP-ribose) Polymerase (PARP) enzyme. Particularly, this enzyme is involved in repair of damages to single-strand DNA, thus decreasing the chances of generating double-strand breaks in the genome. Therefore, the concept to block PARP enzymes by PARP inhibitor (PARPi) was appreciated in cancer treatment. PARPi has been designed and tested for many years and became a potential supplement for the conventional chemotherapy. However, increasing evidence indicates the appearance of the resistance to this treatment. Specifically, cancer cells may acquire new mutations or events that overcome the positive effect of these drugs. This paper describes several molecular mechanisms of PARPi resistance which were reported most recently, and summarizes some strategies to reverse this type of drug resistance. Ivyspring International Publisher 2017-02-17 /pmc/articles/PMC5332874/ /pubmed/28255272 http://dx.doi.org/10.7150/ijbs.17240 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Kim, Yevgeniy Kim, Aleksei Sharip, Ainur Sharip, Aigul Jiang, Juhong Yang, Qing Xie, Yingqiu Reverse the Resistance to PARP Inhibitors |
title | Reverse the Resistance to PARP Inhibitors |
title_full | Reverse the Resistance to PARP Inhibitors |
title_fullStr | Reverse the Resistance to PARP Inhibitors |
title_full_unstemmed | Reverse the Resistance to PARP Inhibitors |
title_short | Reverse the Resistance to PARP Inhibitors |
title_sort | reverse the resistance to parp inhibitors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332874/ https://www.ncbi.nlm.nih.gov/pubmed/28255272 http://dx.doi.org/10.7150/ijbs.17240 |
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