Evidence map›Paper›PMID 27135389›Full record

ReviewCurrent opinion in neurobiology2016

Cell adhesion and invasion mechanisms that guide developing axons.

Caitlin A Short, Edwin A Suarez-Zayas, Timothy M Gomez

Abstract readReview
In one paragraph

Review in Current opinion in neurobiology, 2016. 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
4.2field-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

19 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  9. Multiscale Mechanobiology in Brain Physiology and Diseases.Frontiers in cell and developmental biology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Axon growth regulation by a bistable molecular switch.Proceedings. Biological sciences · 2018
    Article
  17. Article
  18. RACK1 regulates neural development.Neural regeneration research · 2017
    Review
  19. 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

3 authors at 1 institution in 1 country.

Caitlin A ShortDepartment of Neuroscience and Neuroscience Training Program, University of Wisconsin, Madison, WI 53705, United States.
Edwin A Suarez-ZayasDepartment of Neuroscience and Neuroscience Training Program, University of Wisconsin, Madison, WI 53705, United States.
Timothy M GomezDepartment of Neuroscience and Neuroscience Training Program, University of Wisconsin, Madison, WI 53705, United States. Electronic address: tmgomez@wisc.edu.
University of Wisconsin–Madison · US

Funding

NEUROSCIENCE TRAINING PROGRAMT32GM007507 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HALLORAN, MARY C · 1985 to 2017
$9.3M
Molecular mechanisms of growth cone invasionR01NS099405 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI GOMEZ, TIMOTHY M · 2016 to 2019
$1.4M
Modeling Neural Development Using Human iPSCs from TSC PatientsR21NS088477 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI GOMEZ, TIMOTHY M · 2014 to 2015
$414k
Regulation of Axon Guidance by Second MessengerR56NS041564 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI GOMEZ, TIMOTHY M · 2015 to 2015
$374k
NIGMS NIH HHS T32 GM007507NINDS NIH HHS R01 NS099405NINDS NIH HHS R21 NS088477NINDS NIH HHS R56 NS041564
6 · The paper itself

Abstract

Axon extension, guidance and tissue invasion share many similarities to normal cell migration and cancer cell metastasis. Proper cell and growth cone migration requires tightly regulated adhesion complex assembly and detachment from the extracellular matrix (ECM). In addition, many cell types actively remodel the ECM using matrix metalloproteases (MMPs) to control tissue invasion and cell dispersal. Targeting and activating MMPs is a tightly regulated process, that when dysregulated, can lead to cancer cell metastasis. Interestingly, new evidence suggests that growth cones express similar cellular and molecular machinery as migrating cells to clutch retrograde actin flow on ECM proteins and target matrix degradation, which may be used to facilitate axon pathfinding through the basal lamina and across tissues.

Indexed as

AxonsCell AdhesionCell MovementGrowth ConesHumansNeurogenesisNeurons

Identifiers

PMID27135389
PMCPMC4987159
OpenAlexW2344691889

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.