Evidence map›Paper›PMID 28587234›Full record

ReviewInternational journal of molecular sciences2017

Peptidylarginine Deiminases-Roles in Cancer and Neurodegeneration and Possible Avenues for Therapeutic Intervention via Modulation of Exosome and Microvesicle (EMV) Release?

Sigrun Lange, Mark Gallagher, Sharad Kholia, Uchini S Kosgodage, Mariya Hristova, John Hardy, Jameel M Inal

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Extracellular Vesicles in Neurodegenerative Diseases: An Update.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Article
  10. Isolation and characterization of extracellular vesicles and future directions in diagnosis and therapy.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2023
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

7 authors at 3 institutions in 2 countries.

Sigrun LangeDepartment of Biomedical Sciences, University of Westminster, 115, New Cavendish Street, London W1W 6UW, UK. S.Lange@westminster.ac.uk.
Mark GallagherCellular and Molecular Immunology Research Centre, School of Human Sciences, London Metropolitan University, 166-220 Holloway Road, London N7 8DB, UK. m.gallagher@londonmet.ac.uk.
Sharad KholiaMolecular Biotechnology Center, Department of Medical Sciences, University of Turin, Corso Dogliotti 14, 10126 Turin, Italy. sharad.kholia@gmail.com.
Uchini S KosgodageCellular and Molecular Immunology Research Centre, School of Human Sciences, London Metropolitan University, 166-220 Holloway Road, London N7 8DB, UK. uck0002@my.londonmet.ac.uk.
Mariya HristovaInstitute for Women's Health, University College London, 74 Huntley Street, London WC1N 6HX, UK. m.hristova@ucl.ac.uk.
John HardyReta Lila Weston Research Laboratories, Department of Molecular Neuroscience, UCL Institute of Neurology, London WC1N 3BG, UK. j.hardy@ucl.ac.uk.
Jameel M InalCellular and Molecular Immunology Research Centre, School of Human Sciences, London Metropolitan University, 166-220 Holloway Road, London N7 8DB, UK. j.inal@londonmet.ac.uk.
London Metropolitan University · GBUniversity College London · GBUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes and microvesicles (EMVs) are lipid bilayer-enclosed structures released from cells and participate in cell-to-cell communication via transport of biological molecules. EMVs play important roles in various pathologies, including cancer and neurodegeneration. The regulation of EMV biogenesis is thus of great importance and novel ways for manipulating their release from cells have recently been highlighted. One of the pathways involved in EMV shedding is driven by peptidylarginine deiminase (PAD) mediated post-translational protein deimination, which is calcium-dependent and affects cytoskeletal rearrangement amongst other things. Increased PAD expression is observed in various cancers and neurodegeneration and may contribute to increased EMV shedding and disease progression. Here, we review the roles of PADs and EMVs in cancer and neurodegeneration.

Indexed as

AnimalsCell-Derived MicroparticlesCentral Nervous SystemCytoskeletonEnzyme InhibitorsEpigenesis, GeneticExosomesExtracellular VesiclesHistonesHumansNeoplasmsNeurodegenerative DiseasesNeuroprotective AgentsProtein-Arginine DeiminasesProtein BindingProtein Processing, Post-TranslationalEnzyme InhibitorsHistonesNeuroprotective AgentsProtein-Arginine DeiminasescancerChlor-amidine (Cl-Am)cytoskeletondeiminationepigeneticsexosomesextracellular vesicles (EVs)histone H3induced pluripotent stem cells (iPSCs)microvesicles (MVs)neurodegenerationpeptidylarginine deiminases (PADs)

Identifiers

PMID28587234
PMCPMC5486019
OpenAlexW2621053270

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.