Evidence map›Paper›PMID 30441833›Full record

ReviewInternational journal of molecular sciences2018

Emerging Role of Purine Metabolizing Enzymes in Brain Function and Tumors.

Mercedes Garcia-Gil, Marcella Camici, Simone Allegrini, Rossana Pesi, Edoardo Petrotto, Maria Grazia Tozzi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.7field-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

38 citing papers in PubMed, 74 citations in OpenAlex.

  1. Longitudinal untargeted metabolomics of cognitive impairment in Parkinson's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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  5. Review
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  9. Brain and behavioural anomalies caused byLife science alliance · 2025
    Article
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  14. Review
  15. Article
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  18. Article
  19. IncreasedExperimental and therapeutic medicine · 2023
    Article
  20. 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

6 authors at 1 institution in 1 country.

Mercedes Garcia-GilDipartimento di Biologia, Unità di Fisiologia Generale, Via San Zeno 31, 56127 Pisa, Italy. mercedes.garcia@unipi.it.ORCID 0000-0002-1344-2786
Marcella CamiciDipartimento di Biologia, Unità di Biochimica, Via San Zeno 51, 56127 Pisa, Italy. marcella.camici@unipi.it.ORCID 0000-0001-8133-8414
Simone AllegriniDipartimento di Biologia, Unità di Biochimica, Via San Zeno 51, 56127 Pisa, Italy. simone.allegrini@unipi.it.ORCID 0000-0002-7005-654X
Rossana PesiDipartimento di Biologia, Unità di Biochimica, Via San Zeno 51, 56127 Pisa, Italy. rossana.pesi@unipi.it.ORCID 0000-0003-4785-7282
Edoardo PetrottoDipartimento di Biologia, Unità di Biochimica, Via San Zeno 51, 56127 Pisa, Italy. edoardo.petrotto@gmail.com.
Maria Grazia TozziDipartimento di Biologia, Unità di Biochimica, Via San Zeno 51, 56127 Pisa, Italy. maria.grazia.tozzi@unipi.it.ORCID 0000-0002-1075-7096
Istituto di Fisiologia Clinica · IT

Funding

Università di Pisa PRA 2017
6 · The paper itself

Abstract

The growing evidence of the involvement of purine compounds in signaling, of nucleotide imbalance in tumorigenesis, the discovery of purinosome and its regulation, cast new light on purine metabolism, indicating that well known biochemical pathways may still surprise. Adenosine deaminase is important not only to preserve functionality of immune system but also to ensure a correct development and function of central nervous system, probably because its activity regulates the extracellular concentration of adenosine and therefore its function in brain. A lot of work has been done on extracellular 5'-nucleotidase and its involvement in the purinergic signaling, but also intracellular nucleotidases, which regulate the purine nucleotide homeostasis, play unexpected roles, not only in tumorigenesis but also in brain function. Hypoxanthine guanine phosphoribosyl transferase (HPRT) appears to have a role in the purinosome formation and, therefore, in the regulation of purine synthesis rate during cell cycle with implications in brain development and tumors. The final product of purine catabolism, uric acid, also plays a recently highlighted novel role. In this review, we discuss the molecular mechanisms underlying the pathological manifestations of purine dysmetabolisms, focusing on the newly described/hypothesized roles of cytosolic 5'-nucleotidase II, adenosine kinase, adenosine deaminase, HPRT, and xanthine oxidase.

Indexed as

AnimalsBrainBrain Diseases, Metabolic, InbornHumansNeoplasmsPurinesPurinesadenosine deaminaseadenosine kinasecytosolic 5′-nucleotidase IIhypoxanthine guanine phosphoribosyl transferaseuric acidxanthine oxidase

Identifiers

PMID30441833
PMCPMC6274932
OpenAlexW2900850467

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.