Evidence map›Paper›PMID 25491371›Full record

ReviewAdvances in biological regulation2015

NGF and ProNGF: Regulation of neuronal and neoplastic responses through receptor signaling.

Ralph A Bradshaw, Jay Pundavela, Jordane Biarc, Robert J Chalkley, A L Burlingame, Hubert Hondermarck

Open access · greenAbstract readReview
In one paragraph

Review in Advances in biological regulation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 112 citations in OpenAlex.

  1. Pooled it
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  18. Expression of NGF, proNGF, p75Clinics (Sao Paulo, Brazil) · 2024
    Article
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  20. Article

6 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 2 countries.

Ralph A BradshawDept of Pharmaceutical Chemistry, UCSF, San Francisco, CA, USA. Electronic address: rab@cgl.ucsf.edu.
Jay PundavelaSchool of Biomedical Sciences & Pharmacy, Hunter Medical Research Institute, Faculty of Health and Medicine, University of Newcastle, Australia. Electronic address: jay.pundavela@newcastle.edu.au.
Jordane BiarcDept of Pharmaceutical Chemistry, UCSF, San Francisco, CA, USA. Electronic address: jordane.biarc@univ-lyon1.fr.
Robert J ChalkleyDept of Pharmaceutical Chemistry, UCSF, San Francisco, CA, USA. Electronic address: chalkley@cgl.ucsf.edu.
A L BurlingameDept of Pharmaceutical Chemistry, UCSF, San Francisco, CA, USA. Electronic address: alb@cgl.ucsf.edu.
Hubert HondermarckSchool of Biomedical Sciences & Pharmacy, Hunter Medical Research Institute, Faculty of Health and Medicine, University of Newcastle, Australia. Electronic address: hubert.hondermarck@newcastle.edu.au.
University of California, San Francisco · USHunter Medical Research Institute · AUUniversity of Newcastle Australia · AU

Funding

Bio-Organic Biomedical Mass Spectromy ResourceP41GM103481 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURLINGAME, ALMA L · 2012 to 2015
$6.4M
Purchase of Q-Exactive Mass SpectrometerS10OD016229 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURLINGAME, ALMA L · 2013 to 2013
$507k
NIGMS NIH HHS 8P41GM103481NIGMS NIH HHS P41 GM103481NIH HHS 1S10OD016229NIH HHS S10 OD016229
6 · The paper itself

Abstract

Nerve growth factor (NGF) and its precursor (proNGF) are primarily considered as regulators of neuronal function that induce their responses via the tyrosine kinase receptor TrkA and the pan-neurotrophin receptor p75NTR. It has been generally held that NGF exerts its effects primarily through TrkA, inducing a cascade of tyrosine kinase-initiated responses, while proNGF binds more strongly to p75NTR. When this latter entity interacts with a third receptor, sortilin, apoptotic responses are induced in contrast to the survival/differentiation associated with the other two. Recent studies have outlined portions of the downstream phosphoproteome of TrkA in the neuronal PC12 cells and have clarified the contribution of individual docking sites in the TrkA endodomain. The patterns observed showed a similarity with the profile induced by the epidermal growth factor receptor, which is extensively associated with oncogenesis. Indeed, as with other neurotrophic factors, the distribution of TrkA and p75NTR is not limited to neuronal tissue, thus providing an array of targets outside the nervous systems. One such source is breast cancer cells, in which NGF and proNGF stimulate breast cancer cell survival/growth and enhance cell invasion, respectively. This latter activity is exerted via TrkA (as opposed to p75NTR) in conjunction with sortilin. Another tissue overexpressing proNGF is prostate cancer and here the ability of cancer cells to induce neuritogenesis has been implicated in cancer progression. These studies show that the non-neuronal functions of proNGF/NGF are likely integrated with their neuronal activities and point to the clinical utility of these growth factors and their receptors as biomarkers and therapeutic targets for metastasis and cancer pain.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsBreast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMaleNerve Growth FactorNerve Tissue ProteinsNeuronsPC12 CellsProstatic NeoplasmsProtein PrecursorsRatsReceptors, Nerve Growth FactorReceptor, trkAAdaptor Proteins, Vesicular TransportNerve Growth FactorNerve Tissue ProteinsNGF protein, humanNGFR protein, humanpro-nerve growth factor, humanProtein PrecursorsReceptors, Nerve Growth FactorReceptor, trkASortilingrowth factorNGFphosphorylationreceptor tyrosine kinasesignaling

Identifiers

PMID25491371
PMCPMC4426037
OpenAlexW2025968900

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.