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Guantay, María L.; Garro, Cintia A.; Siri, Sebastian; Pansa, María; Ghidelli-Disse, Sonja; Paviolo, Natalia; Racca, Ana; Nicotra, Viviana; Radu, Caius; Bocco, José L.; Felice, Rosana; Gloger, Israel; Muelbaier, Marcel; Drewes, Gerard; Madauss, Kevin; García, Manuela; Gottifredi, Vanesa; Soria, Gastón

Abstract P4-08-09: Deoxycytidine kinase (dCK) inhibition is synthetic lethal with BRCA2-deficiency

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  • Media type: E-Article
  • Title: Abstract P4-08-09: Deoxycytidine kinase (dCK) inhibition is synthetic lethal with BRCA2-deficiency
  • Contributor: Guantay, María L.; Garro, Cintia A.; Siri, Sebastian; Pansa, María; Ghidelli-Disse, Sonja; Paviolo, Natalia; Racca, Ana; Nicotra, Viviana; Radu, Caius; Bocco, José L.; Felice, Rosana; Gloger, Israel; Muelbaier, Marcel; Drewes, Gerard; Madauss, Kevin; García, Manuela; Gottifredi, Vanesa; Soria, Gastón
  • imprint: American Association for Cancer Research (AACR), 2023
  • Published in: Cancer Research
  • Language: English
  • DOI: 10.1158/1538-7445.sabcs22-p4-08-09
  • ISSN: 1538-7445
  • Keywords: Cancer Research ; Oncology
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title> <jats:p>BRCA2 is a well-established cancer driver in several human malignancies. While the remarkable success of PARP inhibitors proved the clinical potential of targeting BRCA deficiencies, the emergence of resistance mechanisms underscores the importance of seeking novel Synthetic Lethal (SL) targets for future drug development efforts. In this work, we performed a BRCA2-centric SL screen with a collection of plant-derived compounds from South America. We identified the steroidal alkaloid Solanocapsine as a selective SL inducer, and we were able to substantially increase its potency by deriving multiple analogs. The use of two complementary chemoproteomic approaches led to the identification of the nucleotide salvage pathway enzyme deoxycytidine kinase (dCK) as Solanocapsine’s target responsible for its BRCA2-liked SL induction. Additional confirmatory evidence was obtained by using a highly specific dCK inhibitor (DI-87), which induces SL in multiple BRCA2-deficient and KO contexts. Interestingly, dCK-induced SL is mechanistically different from the one induced by PARP inhibitors. dCK inhibition generates substantially lower levels of DNA damage, and cytotoxic phenotypes are associated exclusively with mitosis, thus suggesting that the fine-tuning of nucleotide supply in mitosis is critical for the survival of BRCA2-deficient cells. Moreover, by using a xenograft model of contralateral tumors, we show that dCK impairment suffices to trigger SL in-vivo. Taken together, our findings unveil dCK as a promising new target for BRCA2-deficient cancers, which provides future therapeutic alternatives to PARP inhibitors.</jats:p> <jats:p>Citation Format: María L. Guantay, Cintia A. Garro, Sebastian Siri, María Pansa, Sonja Ghidelli-Disse, Natalia Paviolo, Ana Racca, Viviana Nicotra, Caius Radu, José L. Bocco, Rosana Felice, Israel Gloger, Marcel Muelbaier, Gerard Drewes, Kevin Madauss, Manuela García, Vanesa Gottifredi, Gastón Soria. Deoxycytidine kinase (dCK) inhibition is synthetic lethal with BRCA2-deficiency [abstract]. In: Proceedings of the 2022 San Antonio Breast Cancer Symposium; 2022 Dec 6-10; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2023;83(5 Suppl):Abstract nr P4-08-09.</jats:p>