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Ovarian and uterine carcinosarcomas are sensitive in vitro and in vivo to elimusertib, a novel ataxia-telangiectasia and Rad3-related (ATR) kinase inhibitor
- Manavella, Diego D.;
- McNamara, Blair;
- Harold, Justin;
- Bellone, Stefania;
- Hartwich, Tobias Max Philipp;
- ... Choi, Jungmin;
- 외 17명
WEB OF SCIENCE
8SCOPUS
8초록
Background Carcinosarcoma of the ovary (OCS) and uterus (UCS) are rare highly aggressive malignancies. Ataxia-telangiectasia-and-Rad3-related (ATR) kinase and homologous recombination play a pivotal role in DNA damage repair. Homologous recombination deficiency (HRD) has been demonstrated in >30% of OCS/UCS. We investigated the preclinical activity of elimusertib, a selective ATR kinase inhibitor, against carcinosarcoma (CS) cell lines and xenografts. Methods Sensitivity to elimusertib was evaluated in vitro against nine whole exome-sequenced (WES) primary CS cell lines and in vivo against HRD CS xenografts. Western blots were performed to determine baseline ATR and p-ATR protein expression in CS, and ATR pathway downstream effectors and apoptosis markers in CS HRD cell lines after Elimusertib treatment. Results Out of the 9 CS cell lines, 3 harbored HRD and 6 homologous recombination proficient (HRP) features. Most of CS (i.e., 7/9 = 85%) were found to be sensitive to Elimusertib in vitro. Among the 5 primary CS cell lines with a high-grade pure serous epithelial component, HRD cell lines were more sensitive to elimusertib than HRP tumors (mean IC50 ± SEM HRD CS = 61.3 nM ±15.2 vs HRP = 361.6 nM ±24.4 (p = 0.01)). Baseline ATR and p-ATR protein expression was higher in HRD CS cell lines. Elimusertib showed tumor growth inhibition in HRD CS xenografts (p < 0.0001) and increased overall animal survival (p < 0.0001). Western blot demonstrated dose-dependent inhibition of ATR, p-ATR and its downstream effector p-CHK1, and a dose-dependent increase in caspase-3 expression. Conclusions Elimusertib is preclinically active in vitro and in vivo against primary CS cell lines and xenografts, respectively. CS models harboring HRD or with pure/mixed endometrioid histology demonstrated higher sensitivity to ATR inhibition. Clinical trials with elimusertib in CS patients are warranted.
키워드
- 제목
- Ovarian and uterine carcinosarcomas are sensitive in vitro and in vivo to elimusertib, a novel ataxia-telangiectasia and Rad3-related (ATR) kinase inhibitor
- 저자
- Manavella, Diego D.; McNamara, Blair; Harold, Justin; Bellone, Stefania; Hartwich, Tobias Max Philipp; Yang-Hartwich, Yang; Mutlu, Levent; Zipponi, Margherita; Demirkiran, Cem; Verzosa, Miguel Skyler; Altwerger, Gary; Ratner, Elena; Huang, Gloria S.; Clark, Mitchell; Andikyan, Vaagn; Azodi, Masoud; Schwartz, Peter E.; Dottino, Peter R.; Choi, Jungmin; Alexandrov, Ludmil B.; Buza, Natalia; Hui, Pei; Santin, Alessandro D.
- 발행일
- 2023-02
- 유형
- Article
- 권
- 169
- 페이지
- 98 ~ 105
- 언어
- ENG
- 출판사
- Academic Press
- 발행국가
- 미국
- 분량
- 8 페이지
- ISSN
- E 1095-6859
P 0090-8258