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Advances in using PARP inhibitors to treat cancer

The poly (ADP-ribose) polymerase (PARP) family of enzymes plays a critical role in the maintenance of DNA integrity as part of the base excision pathway of DNA repair. PARP1 is overexpressed in a variety of cancers, and its expression has been associated with overall prognosis in cancer, especially...

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Detalles Bibliográficos
Autores principales: Kummar, Shivaani, Chen, Alice, Parchment, Ralph E, Kinders, Robert J, Ji, Jay, Tomaszewski, Joseph E, Doroshow, James H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312820/
https://www.ncbi.nlm.nih.gov/pubmed/22401667
http://dx.doi.org/10.1186/1741-7015-10-25
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author Kummar, Shivaani
Chen, Alice
Parchment, Ralph E
Kinders, Robert J
Ji, Jay
Tomaszewski, Joseph E
Doroshow, James H
author_facet Kummar, Shivaani
Chen, Alice
Parchment, Ralph E
Kinders, Robert J
Ji, Jay
Tomaszewski, Joseph E
Doroshow, James H
author_sort Kummar, Shivaani
collection PubMed
description The poly (ADP-ribose) polymerase (PARP) family of enzymes plays a critical role in the maintenance of DNA integrity as part of the base excision pathway of DNA repair. PARP1 is overexpressed in a variety of cancers, and its expression has been associated with overall prognosis in cancer, especially breast cancer. A series of new therapeutic agents that are potent inhibitors of the PARP1 and PARP2 isoforms have demonstrated important clinical activity in patients with breast or ovarian cancers that are caused by mutations in either the BRCA1 or 2 genes. Results from such studies may define a new therapeutic paradigm, wherein simultaneous loss of the capacity to repair DNA damage may have antitumor activity in itself, as well as enhance the antineoplastic potential of cytotoxic chemotherapeutic agents.
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spelling pubmed-33128202012-03-27 Advances in using PARP inhibitors to treat cancer Kummar, Shivaani Chen, Alice Parchment, Ralph E Kinders, Robert J Ji, Jay Tomaszewski, Joseph E Doroshow, James H BMC Med Minireview The poly (ADP-ribose) polymerase (PARP) family of enzymes plays a critical role in the maintenance of DNA integrity as part of the base excision pathway of DNA repair. PARP1 is overexpressed in a variety of cancers, and its expression has been associated with overall prognosis in cancer, especially breast cancer. A series of new therapeutic agents that are potent inhibitors of the PARP1 and PARP2 isoforms have demonstrated important clinical activity in patients with breast or ovarian cancers that are caused by mutations in either the BRCA1 or 2 genes. Results from such studies may define a new therapeutic paradigm, wherein simultaneous loss of the capacity to repair DNA damage may have antitumor activity in itself, as well as enhance the antineoplastic potential of cytotoxic chemotherapeutic agents. BioMed Central 2012-03-09 /pmc/articles/PMC3312820/ /pubmed/22401667 http://dx.doi.org/10.1186/1741-7015-10-25 Text en Copyright ©2012 Kummar et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Minireview
Kummar, Shivaani
Chen, Alice
Parchment, Ralph E
Kinders, Robert J
Ji, Jay
Tomaszewski, Joseph E
Doroshow, James H
Advances in using PARP inhibitors to treat cancer
title Advances in using PARP inhibitors to treat cancer
title_full Advances in using PARP inhibitors to treat cancer
title_fullStr Advances in using PARP inhibitors to treat cancer
title_full_unstemmed Advances in using PARP inhibitors to treat cancer
title_short Advances in using PARP inhibitors to treat cancer
title_sort advances in using parp inhibitors to treat cancer
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312820/
https://www.ncbi.nlm.nih.gov/pubmed/22401667
http://dx.doi.org/10.1186/1741-7015-10-25
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