Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

PPP2R1A mutations cause ATR inhibitor sensitivity in ovarian clear cell carcinoma.

Title: PPP2R1A mutations cause ATR inhibitor sensitivity in ovarian clear cell carcinoma.
Authors: Stewart, J; Krastev, DB; Brough, R; Zatreanu, D; Song, F; Baxter, JS; Sridhar, S; Frankum, J; Konde, A; Yang, W; Haider, S; Alexander, J; Betteridge, K; Gulati, A; Attygalle, AD; Vroobel, K; Natrajan, R; Khalique, S; Roumeliotis, TI; Choudhary, JS; Yeung, J; Wicks, AJ; Marlow, R; Banerjee, S; Pettitt, SJ; Tutt, ANJ; Lord, CJ
Contributors: Krastev, Dragomir; Song, Feifei; Haider, Syed; Natrajan, Rachael; Khalique, Saira; Roumeliotis, Theodoros; Choudhary, Jyoti; Yeung, Chit Sum Jason; Pettitt, Stephen; Tutt, Andrew; Lord, Christopher
Publisher Information: SPRINGERNATURE
Publication Year: 2025
Collection: The Institute of Cancer Research (ICR): Publications Repository
Subject Terms: Science & Technology; Life Sciences & Biomedicine; Biochemistry & Molecular Biology; Oncology; Cell Biology; Genetics & Heredity; SOMATIC MUTATIONS; DNA-REPLICATION; CANCER; PHOSPHORYLATION; DAMAGE; PP2A
Subject Geographic: England
Description: Identification of ARID1A/ATR synthetic lethality led to ATR inhibitor phase II trials in ovarian clear cell carcinoma (OCCC), a cancer of unmet need. Using multiple CRISPR-Cas9 mutagenesis and interference screens, we show that inactivation of protein phosphatase 2A (PP2A) subunits, including PPP2R1A, enhance ATRi sensitivity in ARID1A mutant OCCC. Analysis of a new OCCC cohort indicates that 52% possess oncogenic PPP2R1A p.R183 mutations and of these, one half possessed both ARID1A as well as PPP2R1A mutations. Using CRISPR-prime editing to generate new isogenic models of PPP2R1A mutant OCCC, we found that PPP2R1A p.R183W and p.R183P mutations cause ATRi-induced S phase stress, premature mitotic entry, genomic instability and ATRi sensitivity in OCCC tumour cells. p.R183 mutation also enhanced both in vitro and in vivo ATRi sensitivity in preclinical models of ARID1A mutant OCCC. These results argue for the assessment of PPP2R1A mutations as a biomarker of ATRi sensitivity.
Document Type: article in journal/newspaper
File Description: Print-Electronic; application/pdf
Language: English
ISSN: 1476-5594; 0950-9232
Relation: Oncogene, 2025; https://repository.icr.ac.uk/handle/internal/6575
Availability: https://repository.icr.ac.uk/handle/internal/6575
Rights: http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.5493D8FD
Database: BASE