Evidence map›Paper›PMID 34179015›Full record

ReviewFrontiers in cell and developmental biology2021

HGF and MET: From Brain Development to Neurological Disorders.

Claudia Desole, Simona Gallo, Annapia Vitacolonna, Francesca Montarolo, Antonio Bertolotto, Denis Vivien, Paolo Comoglio, Tiziana Crepaldi

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 123 citations in OpenAlex.

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  2. Plasma proteomic profile of inflammatory depressive symptoms.Brain, behavior, & immunity - health · 2026
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  6. Pathway-level proteomics identifies subcellular trafficking dysregulation as a molecular signature in severe traumatic brain injury.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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31 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

8 authors at 6 institutions in 2 countries.

Claudia DesoleDepartment of Oncology, University of Turin, Turin, Italy.
Simona GalloDepartment of Oncology, University of Turin, Turin, Italy.
Annapia VitacolonnaDepartment of Oncology, University of Turin, Turin, Italy.
Francesca MontaroloNeuroscience Institute Cavalieri Ottolenghi, Orbassano, Italy.
Antonio BertolottoNeuroscience Institute Cavalieri Ottolenghi, Orbassano, Italy.
Denis VivienINSERM U1237, University of Caen, Gyp Cyceron, Caen, France.
Paolo ComoglioIFOM, FIRC Institute for Molecular Oncology, Milan, Italy.
Tiziana CrepaldiDepartment of Oncology, University of Turin, Turin, Italy.
Candiolo Cancer Institute · ITUniversity of Turin · ITCyceron · FRFIRC Institute of Molecular Oncology · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITNeuroscience Institute · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocyte growth factor (HGF) and its tyrosine kinase receptor, encoded by the MET cellular proto-oncogene, are expressed in the nervous system from pre-natal development to adult life, where they are involved in neuronal growth and survival. In this review, we highlight, beyond the neurotrophic action, novel roles of HGF-MET in synaptogenesis during post-natal brain development and the connection between deregulation of MET expression and developmental disorders such as autism spectrum disorder (ASD). On the pharmacology side, HGF-induced MET activation exerts beneficial neuroprotective effects also in adulthood, specifically in neurodegenerative disease, and in preclinical models of cerebral ischemia, spinal cord injuries, and neurological pathologies, such as Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), and multiple sclerosis (MS). HGF is a key factor preventing neuronal death and promoting survival through pro-angiogenic, anti-inflammatory, and immune-modulatory mechanisms. Recent evidence suggests that HGF acts on neural stem cells to enhance neuroregeneration. The possible therapeutic application of HGF and HGF mimetics for the treatment of neurological disorders is discussed.

Indexed as

amyotrophic lateral sclerosisautismcerebral ischemiaHGFMETmultiple sclerosisspinal cord injurysynaptogenesis

Identifiers

PMID34179015
PMCPMC8220160
OpenAlexW3168550974

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.