Evidence map›Paper›PMID 28261054›Full record

ReviewFrontiers in neuroscience2017

The Autophagy Machinery: A New Player in Chemotactic Cell Migration.

Pierre-Michaël Coly, Pierrick Gandolfo, Hélène Castel, Fabrice Morin

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. TRP Channels in Brain Tumors.Frontiers in cell and developmental biology · 2021
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Upgraded role of autophagy in colorectal carcinomas.World journal of gastrointestinal oncology · 2018
    Article
  15. Article
  16. Article
  17. Fluid Shear Stress Promotes Autophagy in Hepatocellular Carcinoma Cells.International journal of biological sciences · 2018
    Article
  18. Review
  19. 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

4 authors at 3 institutions in 1 country.

Pierre-Michaël ColyNormandie Univ, UNIROUEN, Institut National de la Santé et de la Recherche Médicale (INSERM), DC2NRouen, France; Institute for Research and Innovation in BiomedicineRouen, France.
Pierrick GandolfoNormandie Univ, UNIROUEN, Institut National de la Santé et de la Recherche Médicale (INSERM), DC2NRouen, France; Institute for Research and Innovation in BiomedicineRouen, France.
Hélène CastelNormandie Univ, UNIROUEN, Institut National de la Santé et de la Recherche Médicale (INSERM), DC2NRouen, France; Institute for Research and Innovation in BiomedicineRouen, France.
Fabrice MorinNormandie Univ, UNIROUEN, Institut National de la Santé et de la Recherche Médicale (INSERM), DC2NRouen, France; Institute for Research and Innovation in BiomedicineRouen, France.
Université de Rouen Normandie · FRInserm · FRNormandie Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a highly conserved self-degradative process that plays a key role in diverse cellular processes such as stress response or differentiation. A growing body of work highlights the direct involvement of autophagy in cell migration and cancer metastasis. Specifically, autophagy has been shown to be involved in modulating cell adhesion dynamics as well as epithelial-to-mesenchymal transition. After providing a general overview of the mechanisms controlling autophagosome biogenesis and cell migration, we discuss how chemotactic G protein-coupled receptors, through the repression of autophagy, may orchestrate membrane trafficking and compartmentation of specific proteins at the cell front in order to support the critical steps of directional migration.

Indexed as

autophagosome biogenesiscell adhesionchemotactic migrationCXCR4GPCRurotensin II

Identifiers

PMID28261054
PMCPMC5311050
OpenAlexW2588507388

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.