Evidence map›Paper›PMID 31500300›Full record

ArticleCancers2019

Anthracyclines Suppress Both NADPH Oxidase- Dependent and -Independent NETosis in Human Neutrophils.

Meraj A Khan, Adam D'Ovidio, Harvard Tran, Nades Palaniyar

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Role of phagocyte extracellular traps duringFrontiers in microbiology · 2023
    Review
  12. Review
  13. Article
  14. Potential Role of Neutrophil Extracellular Traps in Cardio-Oncology.International journal of molecular sciences · 2022
    Review
  15. Inhibition of NETosis for treatment purposes: friend or foe?Molecular and cellular biochemistry · 2022
    Review
  16. Article
  17. Article
  18. Review
  19. Neutrophil extracellular traps in gastrointestinal cancer.World journal of gastroenterology · 2021
    Review
  20. Review
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

4 authors at 1 institution in 1 country.

Meraj A KhanProgram in Translational Medicine, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, 686, Bay St., Toronto, ON M5G 0A4, Canada.
Adam D'OvidioProgram in Translational Medicine, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, 686, Bay St., Toronto, ON M5G 0A4, Canada.
Harvard TranProgram in Translational Medicine, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, 686, Bay St., Toronto, ON M5G 0A4, Canada.
Nades PalaniyarProgram in Translational Medicine, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, 686, Bay St., Toronto, ON M5G 0A4, Canada. nades.palaniyar@sickkids.ca.ORCID 0000-0002-2170-8548
University of Toronto · CA

Funding

Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada RGPIN436250-13CIHR MOP-111012Cystic Fibrosis Canada Discovery Grant 3180
6 · The paper itself

Abstract

Neutrophil extracellular traps (NETs) are cytotoxic DNA-protein complexes that play positive and negative roles in combating infection, inflammation, organ damage, autoimmunity, sepsis and cancer. However, NETosis regulatory effects of most of the clinically used drugs are not clearly established. Several recent studies highlight the relevance of NETs in promoting both cancer cell death and metastasis. Here, we screened the NETosis regulatory ability of 126 compounds belonging to 39 classes of drugs commonly used for treating cancer, blood cell disorders and other diseases. Our studies show that anthracyclines (e.g., epirubicin, daunorubicin, doxorubicin, and idarubicin) consistently suppress both NADPH oxidase-dependent and -independent types of NETosis in human neutrophils, ex vivo. The intercalating property of anthracycline may be enough to alter the transcription initiation and lead NETosis inhibition. Notably, the inhibitory doses of anthracyclines neither suppress the production of reactive oxygen species that are necessary for antimicrobial functions nor induce apoptotic cell death in neutrophils. Therefore, anthracyclines are a major class of drug that suppresses NETosis. The dexrazoxane, a cardioprotective agent, used for limiting the side effects of anthracyclines, neither affect NETosis nor alter the ability of anthracyclines to suppress NETosis. Hence, at correct doses, anthracyclines together with dexrazoxane could be considered as a therapeutic candidate drug for suppressing unwanted NETosis in NET-related diseases.

Indexed as

anthracyclinesDNA-metabolism inhibitorsdrug screeningneutrophil extracellular trap (NET)Nox-dependent and -independent NETosis

Identifiers

PMID31500300
PMCPMC6770146
OpenAlexW2972184654

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.