专题:PARP inhibition in cancer therapy

This cluster of papers focuses on the use of Poly(ADP-ribose) Polymerase (PARP) inhibitors, such as Olaparib and Niraparib, as a targeted therapy for cancer, particularly in the context of BRCA mutations and DNA repair deficiency. The concept of synthetic lethality, homologous recombination, and the therapeutic potential of PARP inhibitors in various cancers, including platinum-sensitive ovarian cancer, are extensively explored.
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PARP and Androgen-Signaling Inhibition plus ADT in Metastatic Prostate Cancer

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Evaluation of Regorafenib in Newly Diagnosed and Recurrent Glioblastoma: GBM AGILE Phase II/III Bayesian Randomized Platform Trial

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Rethinking ovarian cancer III: the past decade and future directions

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Pembrolizumab plus weekly paclitaxel in platinum-resistant recurrent ovarian cancer (ENGOT-ov65/KEYNOTE-B96): a multicentre, randomised, double-blind, phase 3 study

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Overall survival with relacorilant and nab-paclitaxel in patients with platinum-resistant ovarian cancer (ROSELLA): a phase 3 randomised controlled trial

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Pembrolizumab and olaparib in homologous-recombination-deficient metastatic pancreatic cancer: the phase 2 POLAR trial

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Replicative gaps in DNA damage tolerance, genome instability, and cancer therapy

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Ovarian cancer

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Homologous recombination deficiency and hemizygosity drive resistance in breast cancer

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BCDX2–CX3 and DX2–CX3 complexes assemble and stabilize RAD51 filaments

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