Web of Science: 65 citas, Scopus: 62 citas, Google Scholar: citas,
RAD51 foci as a functional biomarker of homologous recombination repair and PARP inhibitor resistance in germline BRCA-mutated breast cancer
Cruz, C. (Vall d'Hebron Institut d'Oncologia)
Castroviejo-Bermejo, M. (Experimental Therapeutics Group)
Gutiérrez-Enríquez, S. (Oncogenetics Group)
Llop-Guevara, A. (Experimental Therapeutics Group)
Ibrahim, Y.H. (Experimental Therapeutics Group)
Gris-Oliver, A. (Experimental Therapeutics Group)
Bonache, S. (Oncogenetics Group)
Morancho, B. (Vall d'Hebron Institut d'Oncologia)
Bruna, A. (Cancer Research UK Cambridge Institute. University of Cambridge)
Rueda, O.M. (Cancer Research UK Cambridge Institute. University of Cambridge)
Lai, Z. (AstraZeneca (USA))
Polanska, U.M. (Cancer Research UK. Cambridge Institute)
Jones, G.N. (Cancer Research UK. Cambridge Institute)
Kristel, P. (The Netherlands Cancer Institute)
de Bustos, L. (Experimental Therapeutics Group)
Guzman, M. (Experimental Therapeutics Group)
Rodríguez, O. (Experimental Therapeutics Group)
Grueso, J. (Experimental Therapeutics Group)
Montalban, G. (Oncogenetics Group)
Caratú, G. (Cancer Genomics Group)
Mancuso, F. (Cancer Genomics Group)
Fasani, R. (Vall d'Hebron Institut d'Oncologia)
Jiménez, J. (Vall d'Hebron Institut d'Oncologia)
Howat, W.J. (Cancer Research UK. Cambridge Institute)
Dougherty, B. (AstraZeneca (USA))
Vivancos, A. (Cancer Genomics Group)
Nuciforo, Paolo (Vall d'Hebron Institut d'Oncologia)
Serres-Créixams, X. (Department of Radiology)
Rubio Rodríguez, Isabel Teresa (Hospital de la Vall d'Hebron)
Oaknin, A. (Vall d'Hebron Institut d'Oncologia)
Cadogan, E. (Cancer Research UK. Cambridge Institute)
Barrett, J.C. (AstraZeneca (USA))
Caldas, C. (Cambridge University. NIHR Cambridge Biomedical Research Centre and Cambridge Experimental Cancer Medicine Centre (UK))
Baselga Torres, Josep, 1959-, (Memorial Sloan Kettering Cancer Center (USA))
Saura, Cristina (Vall d'Hebron Institut d'Oncologia)
Cortes, Javier (Vall d'Hebron Institut d'Oncologia)
Arribas, Joaquín V. (Vicente) (Universitat Autònoma de Barcelona. Departament de Bioquímica i Biologia Molecular)
Jonkers, J. (Cancer Genomics Group)
Díez, Orland (Hospital Vall d'Hebron)
O'Connor, M.J. (Oncology Innovative Medicine and Early Development Biotech Unit. AstraZeneca (UK))
Balmaña Gelpí, Judith (Vall d'Hebron Institut d'Oncologia)
Serra, Violeta (Vall d'Hebron Institut d'Oncologia)

Fecha: 2018
Resumen: BRCA1 and BRCA2 (BRCA1/2) -deficient tumors display impaired homologous recombination repair (HRR) and enhanced sensitivity to DNA damaging agents or to poly(ADP-ribose) polymerase (PARP) inhibitors (PARPi). Their efficacy in germline BRCA1/2 (gBRCA1/2)-mutated metastatic breast cancers has been recently confirmed in clinical trials. Numerous mechanisms of PARPi resistance have been described, whose clinical relevance in gBRCA-mutated breast cancer is unknown. This highlights the need to identify functional biomarkers to better predict PARPi sensitivity. We investigated the in vivo mechanisms of PARPi resistance in gBRCA1 patient-derived tumor xenografts (PDXs) exhibiting differential response to PARPi. Analysis included exome sequencing and immunostaining of DNA damage response proteins to functionally evaluate HRR. Findings were validated in a retrospective sample set from gBRCA1/2-cancer patients treated with PARPi. RAD51 nuclear foci, a surrogate marker of HRR functionality, were the only common feature in PDX and patient samples with primary or acquired PARPi resistance. Consistently, low RAD51 was associated with objective response to PARPi. Evaluation of the RAD51 biomarker in untreated tumors was feasible due to endogenous DNA damage. In PARPi-resistant gBRCA1 PDXs, genetic analysis found no in-frame secondary mutations, but BRCA1 hypomorphic proteins in 60% of the models, TP53BP1 -loss in 20% and RAD51 -amplification in one sample, none mutually exclusive. Conversely, one of three PARPi-resistant gBRCA2 tumors displayed BRCA2 restoration by exome sequencing. In PDXs, PARPi resistance could be reverted upon combination of a PARPi with an ataxia-telangiectasia mutated (ATM) inhibitor. Detection of RAD51 foci in gBRCA tumors correlates with PARPi resistance regardless of the underlying mechanism restoring HRR function. This is a promising biomarker to be used in the clinic to better select patients for PARPi therapy. Our study also supports the clinical development of PARPi combinations such as those with ATM inhibitors.
Nota: Altres ajuts: European Research Area-NET, Transcan-2 (AC15/00063), Asociación Española Contra el Cáncer (LABAE16020PORTT) i AIOC15152806CRUZ, Generalitat de Catalunya(PERIS, SLT002/16/00477
Nota: Número d'acord de subvenció ISCIII/FIS/PI17/01080
Nota: Número d'acord de subvenció ISCIII/FIS/PI12-02606
Nota: Número d'acord de subvenció ISCIII/FIS/PI15-00355
Nota: Número d'acord de subvenció ISCIII/FIS/PI13-01711
Nota: Número d'acord de subvenció ISCIII/CP14-00228
Nota: Número d'acord de subvenció ISCIII/CP10-00617
Nota: Número d'acord de subvenció AGAUR/2014/SGR-1331
Nota: Número d'acord de subvenció AGAUR/2017/SGR-540
Derechos: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. Per a usos comercials contactar amb: journals.permissions@oup.com Creative Commons
Lengua: Anglès
Documento: article ; recerca ; publishedVersion
Materia: Germline BRCA ; PARP inhibitor resistance ; Homologous recombination ; RAD51 ; TP53BP1 ; ATM
Publicado en: Annals of oncology, Vol. 29, Issue 5 (May 2018) , p. 1203-1210, ISSN 1569-8041

DOI: 10.1093/annonc/mdy099
PMID: 29635390

8 p, 473.7 KB

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 Registro creado el 2018-06-18, última modificación el 2020-08-08

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