Evidence map›Paper›PMID 34549724›Full record

ArticleJCI insight2021

SLFN11 captures cancer-immunity interactions associated with platinum sensitivity in high-grade serous ovarian cancer.

Claudia Winkler, Matthew King, Julie Berthe, Domenico Ferraioli, Anna Garuti, Federica Grillo, Jaime Rodriguez-Canales, Lorenzo Ferrando, Nicolas Chopin, Isabelle Ray-Coquard and 6 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  8. MET and SLFN11 as a Players in the SCLC Molecular Subtyping Game.International journal of molecular sciences · 2025
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  20. High expression of theAnnals of translational medicine · 2022
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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

16 authors at 6 institutions in 8 countries.

Claudia WinklerBioscience and.
Matthew KingBioscience and.
Julie BertheTranslational Medicine, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.
Domenico FerraioliCentre Léon Bérard, Lyon, France.
Anna GarutiDepartment of Internal Medicine and Medical Specialties and.
Federica GrilloDepartment of Integrated Surgical and Diagnostic Sciences, University of Genova, Genova, Italy.
Jaime Rodriguez-CanalesTranslational Medicine Pathology, Oncology R&D, AstraZeneca, Gaithersburg, Maryland, USA.
Lorenzo FerrandoDepartment of Internal Medicine and Medical Specialties and.
Nicolas ChopinCentre Léon Bérard, Lyon, France.
Isabelle Ray-CoquardCentre Léon Bérard, Lyon, France.
Oona DelpuechBioscience and.
Darawan RinchaiCancer Research Department, Sidra Medicine, Doha, Qatar.
Davide BedognettiDepartment of Internal Medicine and Medical Specialties and.
Alberto BallestreroDepartment of Internal Medicine and Medical Specialties and.
Elisabetta LeoBioscience and.
Gabriele ZoppoliDepartment of Internal Medicine and Medical Specialties and.
Bioscience (China) · CNCentre Léon Bérard · FROspedale Policlinico San Martino · ITAstraZeneca (Netherlands) · NLAstraZeneca (United Kingdom) · GBHamad bin Khalifa University · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large independent analyses on cancer cell lines followed by functional studies have identified Schlafen 11 (SLFN11), a putative helicase, as the strongest predictor of sensitivity to DNA-damaging agents (DDAs), including platinum. However, its role as a prognostic biomarker is undefined, partially due to the lack of validated methods to score SLFN11 in human tissues. Here, we implemented a pipeline to quantify SLFN11 in human cancer samples. By analyzing a cohort of high-grade serous ovarian carcinoma (HGSOC) specimens before platinum-based chemotherapy treatment, we show, for the first time to our knowledge, that SLFN11 density in both the neoplastic and microenvironmental components was independently associated with favorable outcome. We observed SLFN11 expression in both infiltrating innate and adaptive immune cells, and analyses in a second, independent, cohort revealed that SLFN11 was associated with immune activation in HGSOC. We found that platinum treatments activated immune-related pathways in ovarian cancer cells in an SLFN11-dependent manner, representative of tumor-immune transactivation. Moreover, SLFN11 expression was induced in activated, isolated immune cell subpopulations, hinting that SLFN11 in the immune compartment may be an indicator of immune transactivation. In summary, we propose SLFN11 is a dual biomarker capturing simultaneously interconnected immunological and cancer cell-intrinsic functional dispositions associated with sensitivity to DDA treatment.

Indexed as

Adaptive ImmunityAgedAntineoplastic AgentsBiomarkers, TumorCell Line, TumorCisplatinDatabases, GeneticDrug Resistance, NeoplasmFemaleHumansImmunity, InnateLymphocyte CountLymphocytesLymphocytes, Tumor-InfiltratingMacrophagesMiddle AgedAntineoplastic AgentsBiomarkers, TumorCisplatinNuclear ProteinsRNASLFN11 protein, humanBioinformaticsCancerCell BiologyCellular immune responseOncology

Identifiers

PMID34549724
PMCPMC8492341
OpenAlexW3201414411

What OpenQuestion holds

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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.