PURPOSE
VIOLETTE (NCT03330847) assessed olaparib alone or with ceralasertib (ATR inhibitor) or adavosertib (WEE1 inhibitor) as second-/third-line treatment in three molecular strata of patients with previously treated, PARP inhibitor-naïve, advanced triple-negative breast cancer (TNBC).
PATIENTS AND METHODS
Patients...
A. Tutt, Z. Nowecki, R. Szoszkiewicz et al.· Clinical Cancer Research· 0 citations
Cancer cells lacking BRCA1 or BRCA2 must adapt to proliferate despite pervasive genomic instability. To delineate BRCA1- and BRCA2-specific adaptation landscapes, we developed an isogenic screening platform enabling acute depletion of either protein. Genetic interaction profiling revealed hundreds of genes with shared,...
François Dossin, Mikaël Attia, Fabricio Montero-Zúñiga et al.· Molecules and Cells· 0 citations
Successful cancer immunotherapy requires not only tumor cell killing but also the activation of innate and adaptive immune responses. The inhibitor of apoptosis (IAP) proteins cIAP1, cIAP2 and XIAP act as key suppressors of RIPK1-driven immunogenic cell death, thereby enabling tumor immune evasion and limiting the effe...
C. Tiu, Wing Yau, T. Tenev et al.· Nature Communications· 0 citations
BACKGROUND
The randomised phase III OlympiA trial (NCT02032823) compared 1 year of adjuvant olaparib (oral poly-(ADP-ribose) polymerase [PARP] inhibitor) to placebo in 1,836 patients with pathogenic/likely pathogenic BRCA1 or BRCA2 (gBRCApv) germline variants and high-risk human epidermal growth factor receptor 2 (HER2...
J. Garber, D. Cameron, C. Campbell et al.· Annals of Oncology· 1 citation
It is reported that DDIAS is a DNA-binding effector of the CIP2A pathway in human cells and proposed that DDIAS defines a mitotic DNA repair system downstream of CIP2A that mitigates the threat of mitotic ssDNA for genome integrity.
Yibo Xue, Faisal Bin Rashed, Daniel Y. L. Mao et al.· Molecules and Cells· 1 citation
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