Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies

The PARP inhibitor olaparib is an approved treatment method for women with BRCA1 and BRCA2 mutation associated cancers. Here the authors show that olaparib can contribute to synthetic viability of cells if PARP1 is inhibited before BRCA2 loss.

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Autores principales: Xia Ding, Arnab Ray Chaudhuri, Elsa Callen, Yan Pang, Kajal Biswas, Kimberly D. Klarmann, Betty K. Martin, Sandra Burkett, Linda Cleveland, Stacey Stauffer, Teresa Sullivan, Aashish Dewan, Hanna Marks, Anthony T. Tubbs, Nancy Wong, Eugen Buehler, Keiko Akagi, Scott E. Martin, Jonathan R. Keller, André Nussenzweig, Shyam K. Sharan
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Lenguaje:EN
Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/cf505f822a744ac9ab12008610c61b55
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spelling oai:doaj.org-article:cf505f822a744ac9ab12008610c61b552021-12-02T14:40:13ZSynthetic viability by BRCA2 and PARP1/ARTD1 deficiencies10.1038/ncomms124252041-1723https://doaj.org/article/cf505f822a744ac9ab12008610c61b552016-08-01T00:00:00Zhttps://doi.org/10.1038/ncomms12425https://doaj.org/toc/2041-1723The PARP inhibitor olaparib is an approved treatment method for women with BRCA1 and BRCA2 mutation associated cancers. Here the authors show that olaparib can contribute to synthetic viability of cells if PARP1 is inhibited before BRCA2 loss.Xia DingArnab Ray ChaudhuriElsa CallenYan PangKajal BiswasKimberly D. KlarmannBetty K. MartinSandra BurkettLinda ClevelandStacey StaufferTeresa SullivanAashish DewanHanna MarksAnthony T. TubbsNancy WongEugen BuehlerKeiko AkagiScott E. MartinJonathan R. KellerAndré NussenzweigShyam K. SharanNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Xia Ding
Arnab Ray Chaudhuri
Elsa Callen
Yan Pang
Kajal Biswas
Kimberly D. Klarmann
Betty K. Martin
Sandra Burkett
Linda Cleveland
Stacey Stauffer
Teresa Sullivan
Aashish Dewan
Hanna Marks
Anthony T. Tubbs
Nancy Wong
Eugen Buehler
Keiko Akagi
Scott E. Martin
Jonathan R. Keller
André Nussenzweig
Shyam K. Sharan
Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies
description The PARP inhibitor olaparib is an approved treatment method for women with BRCA1 and BRCA2 mutation associated cancers. Here the authors show that olaparib can contribute to synthetic viability of cells if PARP1 is inhibited before BRCA2 loss.
format article
author Xia Ding
Arnab Ray Chaudhuri
Elsa Callen
Yan Pang
Kajal Biswas
Kimberly D. Klarmann
Betty K. Martin
Sandra Burkett
Linda Cleveland
Stacey Stauffer
Teresa Sullivan
Aashish Dewan
Hanna Marks
Anthony T. Tubbs
Nancy Wong
Eugen Buehler
Keiko Akagi
Scott E. Martin
Jonathan R. Keller
André Nussenzweig
Shyam K. Sharan
author_facet Xia Ding
Arnab Ray Chaudhuri
Elsa Callen
Yan Pang
Kajal Biswas
Kimberly D. Klarmann
Betty K. Martin
Sandra Burkett
Linda Cleveland
Stacey Stauffer
Teresa Sullivan
Aashish Dewan
Hanna Marks
Anthony T. Tubbs
Nancy Wong
Eugen Buehler
Keiko Akagi
Scott E. Martin
Jonathan R. Keller
André Nussenzweig
Shyam K. Sharan
author_sort Xia Ding
title Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies
title_short Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies
title_full Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies
title_fullStr Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies
title_full_unstemmed Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies
title_sort synthetic viability by brca2 and parp1/artd1 deficiencies
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/cf505f822a744ac9ab12008610c61b55
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