Evidence map›Paper›PMID 33964209›Full record

ArticleCell2021

Neutrophil elastase selectively kills cancer cells and attenuates tumorigenesis.

Chang Cui, Kasturi Chakraborty, Xu Anna Tang, Guolin Zhou, Kelly Q Schoenfelt, Kristen M Becker, Alexandria Hoffman, Ya-Fang Chang, Ariane Blank, Catherine A Reardon and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 242 papers.

0numbers the graph read from it
0cells of the map it votes in
242citing papers in PubMed
31.7field-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

242 citing papers in PubMed, 351 citations in OpenAlex.

  1. Article
  2. Neutrophils in cancer.Nature reviews. Cancer · 2026
    Review
  3. CAR-engineered neutrophils derived from induced pluripotent stem cells: a new frontier in cellular immunotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Article
  5. Article
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  12. PIV, PNI and HALP score for predicting pathological complete response in breast cancer after neoadjuvant chemotherapy: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  13. Review
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182 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 1 country.

Chang CuiCommittee on Cancer Biology, The University of Chicago, Chicago, IL 60637, USA; Ben May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Kasturi ChakrabortyBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Xu Anna TangBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Guolin ZhouBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Kelly Q SchoenfeltBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Kristen M BeckerBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Alexandria HoffmanBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA; Committee on Molecular Metabolism and Nutrition, The University of Chicago, Chicago, IL 60637, USA.
Ya-Fang ChangBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Ariane BlankBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Catherine A ReardonBen May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA.
Hilary A KennyCommittee on Cancer Biology, The University of Chicago, Chicago, IL 60637, USA; Department of Obstetrics and Gynecology, Section of Gynecological Oncology, The University of Chicago, Chicago, IL 60637, USA.
Tomas VaisarDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
Ernst LengyelCommittee on Cancer Biology, The University of Chicago, Chicago, IL 60637, USA; Department of Obstetrics and Gynecology, Section of Gynecological Oncology, The University of Chicago, Chicago, IL 60637, USA; University of Chicago Comprehensive Cancer Center, The University of Chicago, Chicago, IL 60637, USA; Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL 60637, USA.
Geoffrey GreeneCommittee on Cancer Biology, The University of Chicago, Chicago, IL 60637, USA; Ben May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA; University of Chicago Comprehensive Cancer Center, The University of Chicago, Chicago, IL 60637, USA; Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL 60637, USA.
Lev BeckerCommittee on Cancer Biology, The University of Chicago, Chicago, IL 60637, USA; Ben May Department for Cancer Research, The University of Chicago, Chicago, IL 60637, USA; Committee on Molecular Metabolism and Nutrition, The University of Chicago, Chicago, IL 60637, USA; University of Chicago Comprehensive Cancer Center, The University of Chicago, Chicago, IL 60637, USA; Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL 60637, USA. Electronic address: levb@uchicago.edu.
University of Chicago · USUniversity of Washington · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
NIDDK NIH HHS P30 DK017047
6 · The paper itself

Abstract

Cancer cell genetic variability and similarity to host cells have stymied development of broad anti-cancer therapeutics. Our innate immune system evolved to clear genetically diverse pathogens and limit host toxicity; however, whether/how innate immunity can produce similar effects in cancer is unknown. Here, we show that human, but not murine, neutrophils release catalytically active neutrophil elastase (ELANE) to kill many cancer cell types while sparing non-cancer cells. ELANE proteolytically liberates the CD95 death domain, which interacts with histone H1 isoforms to selectively eradicate cancer cells. ELANE attenuates primary tumor growth and produces a CD8

Indexed as

Allosteric RegulationAnimalsCarcinogenesisCD8-Positive T-LymphocytesCell DeathCell Line, TumorCell ProliferationEosinophil Cationic Proteinfas ReceptorHistonesHumansLeukocyte ElastaseMiceNeoplasmsNeutrophilsPancreatic ElastaseELANE protein, humanElane protein, mouseEosinophil Cationic Proteinfas ReceptorHistonesLeukocyte ElastasePancreatic ElastaseProtease InhibitorsProtein IsoformsSecretory Leukocyte Peptidase InhibitorSlpi protein, mousecancerCD95histone H1neutrophil estateneutrophilstherapeuticstumor immunology

Identifiers

PMID33964209
PMCPMC10712736
OpenAlexW3160411478

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.