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Cumulative defects in DNA repair pathways drive the PARP inhibitor response in high-grade serous epithelial ovarian cancer cell lines.
Fleury, Hubert; Carmona, Euridice; Morin, Vincent G; Meunier, Liliane; Masson, Jean-Yves; Tonin, Patricia N; Provencher, Diane; Mes-Masson, Anne-Marie.
Afiliação
  • Fleury H; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada.
  • Carmona E; Institut du cancer de Montréal, Montreal, Canada.
  • Morin VG; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada.
  • Meunier L; Institut du cancer de Montréal, Montreal, Canada.
  • Masson JY; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada.
  • Tonin PN; Institut du cancer de Montréal, Montreal, Canada.
  • Provencher D; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, Canada.
  • Mes-Masson AM; Institut du cancer de Montréal, Montreal, Canada.
Oncotarget ; 8(25): 40152-40168, 2017 Jun 20.
Article em En | MEDLINE | ID: mdl-27374179
PARP inhibitors (PARPi), such as Olaparib, have shown promising results in high-grade serous (HGS) epithelial ovarian cancer (EOC) treatment. PARPi sensitivity has been mainly associated with homologous recombination (HR) deficiency, but clinical trials have shown that predicting actual patient response is complex. Here, we investigated gene expression microarray, HR functionality and Olaparib sensitivity of 18 different HGS EOC cell lines and demonstrate that PARPi sensitivity is not only associated with HR defects. Gene target validation show that down regulation of genes in the nucleotide excision repair (NER) and mismatch repair (MMR) pathways (ERCC8 and MLH1, respectively) increases PARPi response. The highest sensitivity was observed when genes in both the HR and either NER or MMR pathways were concomitantly down regulated. Using clinical samples, patients with these concurrent down regulations could be identified. Based on these results, a novel model to predict PARPi sensitivity is herein proposed. This model implies that the extreme responders identified in clinical trials have deficiencies in HR and either NER or MMR.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ftalazinas / Piperazinas / Transdução de Sinais / Regulação Neoplásica da Expressão Gênica / Reparo do DNA Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ftalazinas / Piperazinas / Transdução de Sinais / Regulação Neoplásica da Expressão Gênica / Reparo do DNA Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article