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annotations Item: Title: Generation of PDX models and in vivo treatment experiments Item: Title: Evaluation of response to therapy in PDXs Item: Title: Targeted sequencing Item: Title: Exome sequencing Item: Title: RNA sequencing Item: Title: BRCA1 isoforms analysis Item: Title: PARylation assay Item: Title: Immunofluorescence and biomarker scoring Item: Title: Statistical analysis Item: Title: Results Children: Item: Title: AZD5305 shows potent and durable antitumor response in HRR-altered PDX models Item: Title: RAD51 foci captures PARPi sensitivity and restoration of HRR functionality Item: Title: AZD5305 inhibits PARylation and enhances biomarkers of DNA damage and replication stress Item: Title: Treatment with AZD5305 elicits profound and durable responses in combination with carboplatin or an ATRi in PARPi-resistant models Item: Title: Discussion Item: Title: Conclusions Item: Title: Acknowledgements Item: Title: References Info: Title: The PARP1 selective inhibitor saruparib 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SBM; licensed version) PARP inhibitors;PARP1 selective;Targeted therapy;Breast cancer;DNA damaging agent;BRCA1/2;RAD51;Homologous recombination deficiency;HRD;Antitumor activity False application/pdf https://doi.org/10.1186/s13073-024-01370-z BioMed Central Genome Medicine, https://doi.org/10.1186/s13073-024-01370-z PARP inhibitors PARP1 selective Targeted therapy Breast cancer DNA damaging agent BRCA1/2 RAD51 Homologous recombination deficiency HRD Antitumor activity The PARP1 selective inhibitor saruparib (AZD5305) elicits potent and durable antitumor activity in patient-derived Andrea Herencia-Ropero Alba Llop-Guevara Anna D. Staniszewska Joanna Domènech-Vivó Eduardo García-Galea Alejandro Moles-Fernández Flaminia Pedretti Heura Domènech Olga Rodríguez Marta Guzmán Enrique J. Arenas Helena Verdaguer Fernando J. Calero-Nieto Sara Talbot Luis Tobalina Elisabetta Leo Alan Lau Paolo Nuciforo Rodrigo Dientsmann Teresa Macarulla Joaquín Arribas Orland Díez Sara Gutiérrez-Enríquez Josep V. Forment Mark J. O’Connor Mark Albertella Judith Balmaña Violeta Serra 10.1186/s13073-024-01370-z 2010-04-23 true springer.com springerlink.com https://doi.org/10.1186/s13073-024-01370-z 10.1186/s13073-024-01370-z 1756-994X journal Genome Medicine The Author(s) 2010-04-23 true 10.1186/s13073-024-01370-z noindex springer.com springerlink.com uuid:2774dfc1-8d6b-4ae6-9e24-75b82d6834ff uuid:127a6fd7-cb9f-4a97-92e1-c958f48e7a05 default 1 converted uuid:2774dfc1-8d6b-4ae6-9e24-75b82d6834ff converted to PDF/A-2b pdfToolbox 2024-08-26T13:47:35Z 2 B Violeta Serra http://orcid.org/0000-0001-6620-1065 http://ns.adobe.com/pdfx/1.3/ pdfx Adobe Document Info PDF eXtension Schema external Mirrors crossmark:MajorVersionDate CrossmarkMajorVersionDate Text external Mirrors crossmark:CrossmarkDomainExclusive CrossmarkDomainExclusive Text internal Mirrors crossmark:DOI doi Text external Mirrors crossmark:CrosMarkDomains CrossMarkDomains seq Text internal A name object indicating whether the document has been modified to include trapping information robots Text internal ID of PDF/X standard GTS_PDFXVersion Text internal Conformance level of PDF/X standard GTS_PDFXConformance Text internal Company creating the PDF Company Text internal Date when document was last modified SourceModified Text http://crossref.org/crossmark/1.0/ crossmark Crossmark Schema internal Usual same as prism:doi DOI Text external The date when a publication was publishe. 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