Evidence map›Paper›PMID 37097615›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2023

RAD51 Foci as a Biomarker Predictive of Platinum Chemotherapy Response in Ovarian Cancer.

Amanda J Compadre, Lillian N van Biljon, Mark C Valentine, Alba Llop-Guevara, Emily Graham, Bisiayo Fashemi, Andrea Herencia-Ropero, Emilee N Kotnik, Isaac Cooper, Shariska P Harrington and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
16.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. RAD51-targeting small molecule degrader sensitizesActa pharmaceutica Sinica. B · 2026
    Article
  3. Article
  4. Clinical and molecular determinants of response to maintenance olaparib for primary and recurrent epithelial ovarian carcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
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  13. The association of the chemotherapy response score and homologous recombination deficiency in patients undergoing interval tumor reductive surgery following neoadjuvant chemotherapy.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2025
    Article
  14. Targeting RAD52 overcomes PARP inhibitor resistance in preclinicalbioRxiv : the preprint server for biology · 2025
    Article
  15. Review
  16. Article
  17. Review
  18. International journal of oncology · 2025
    Review
  19. High Co-Expression ofBiomedicines · 2025
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 4 institutions in 2 countries.

Amanda J Compadre *Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0003-3182-1170
Lillian N van Biljon *Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0009-0000-2179-7782
Mark C ValentineDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0003-3253-267X
Alba Llop-GuevaraExperimental Therapeutics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.ORCID 0000-0002-7913-9472
Emily GrahamDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0009-0006-6705-3766
Bisiayo FashemiDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-1872-8011
Andrea Herencia-RoperoExperimental Therapeutics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.ORCID 0000-0002-1699-0251
Emilee N KotnikDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-9229-3378
Isaac CooperDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0009-0004-2405-5070
Shariska P HarringtonMinnesota Oncology, St. Paul, Minnesota.ORCID 0000-0001-6863-9124
Lindsay M KurokiDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-2141-7310
Carolyn K McCourtDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0003-2229-8971
Andrea R HagemannDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-3484-0046
Premal H ThakerDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-0568-6959
David G MutchDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-6921-1581
Matthew A PowellDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-9001-3862
Lulu SunDepartment of Pathology and Immunology, Washington University, St. Louis, Missouri.ORCID 0000-0001-7543-1532
Nima MosammaparastDepartment of Pathology and Immunology, Washington University, St. Louis, Missouri.ORCID 0000-0001-5453-5914
Violeta SerraExperimental Therapeutics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.ORCID 0000-0001-6620-1065
Peinan ZhaoDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University, St Louis, Missouri.ORCID 0009-0006-0883-0190
Elena LomonosovaDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0009-0005-0970-4615
Dineo KhabeleDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-5151-5210
Mary M MullenDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University, St Louis, Missouri.ORCID 0000-0002-2976-5141
Washington University in St. Louis · USVall d'Hebron Institut de Recerca · ESMinnesota Department of Natural Resources · USUniversitat Autònoma de Barcelona · ES

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NICOLE L NOLLEN · 2012 to 2026
$40.1M
MECHANISM AND REGULATION OF THE DNA ALKYLATION DAMAGE RESPONSER01CA193318 · NCI · WASHINGTON UNIVERSITY · PI MOSAMMAPARAST, NIMA · 2015 to 2024
$3.6M
Integrated Translational Genoproteomics Center at Washington UniversityU10CA180860 · NCI · WASHINGTON UNIVERSITY · PI CHUNG, CHRISTINE H, ELLIS, MATTHEW J · 2014 to 2018
$2.6M
Epigenetic Drug Regimens for Homologous Recombination Proficient Ovarian Cancer - Diversity SupplementR01CA243511 · NCI · WASHINGTON UNIVERSITY · PI KHABELE, DINEO · 2020 to 2024
$2.5M
A SIGNALING PATHWAY SPECIFIC FOR ALKYLATION DAMAGER01CA227001 · NCI · WASHINGTON UNIVERSITY · PI MOSAMMAPARAST, NIMA · 2018 to 2022
$1.8M
NCI NIH HHS P30 CA168524NCI NIH HHS R01 CA193318NCI NIH HHS R01 CA227001NCI NIH HHS R01 CA243511NCI NIH HHS U10 CA180860
6 · The paper itself

Abstract

purposeTo determine the ability of RAD51 foci to predict platinum chemotherapy response in high-grade serous ovarian cancer (HGSOC) patient-derived samples. EXPERIMENTAL

designRAD51 and γH2AX nuclear foci were evaluated by immunofluorescence in HGSOC patient-derived cell lines (n = 5), organoids (n = 11), and formalin-fixed, paraffin-embedded tumor samples (discovery n = 31, validation n = 148). Samples were defined as RAD51-High if >10% of geminin-positive cells had ≥5 RAD51 foci. Associations between RAD51 scores, platinum chemotherapy response, and survival were evaluated.

resultsRAD51 scores correlated with in vitro response to platinum chemotherapy in established and primary ovarian cancer cell lines (Pearson r = 0.96, P = 0.01). Organoids from platinum-nonresponsive tumors had significantly higher RAD51 scores than those from platinum-responsive tumors (P < 0.001). In a discovery cohort, RAD51-Low tumors were more likely to have a pathologic complete response (RR, 5.28; P < 0.001) and to be platinum-sensitive (RR, ∞; P = 0.05). The RAD51 score was predictive of chemotherapy response score [AUC, 0.90; 95% confidence interval (CI), 0.78-1.0; P < 0.001). A novel automatic quantification system accurately reflected the manual assay (92%). In a validation cohort, RAD51-Low tumors were more likely to be platinum-sensitive (RR, ∞; P < 0.001) than RAD51-High tumors. Moreover, RAD51-Low status predicted platinum sensitivity with 100% positive predictive value and was associated with better progression-free (HR, 0.53; 95% CI, 0.33-0.85; P < 0.001) and overall survival (HR, 0.43; 95% CI, 0.25-0.75; P = 0.003) than RAD51-High status.

conclusionsRAD51 foci are a robust marker of platinum chemotherapy response and survival in ovarian cancer. The utility of RAD51 foci as a predictive biomarker for HGSOC should be tested in clinical trials.

Indexed as

Ovarian NeoplasmsPlatinumBiomarkers, TumorCarcinoma, Ovarian EpithelialFemaleHumansRad51 RecombinaseBiomarkers, TumorPlatinumRAD51 protein, humanRad51 Recombinase

Identifiers

PMID37097615
PMCPMC10320470
OpenAlexW4366983131

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.