Evidence map›Paper›PMID 19386095›Full record

ArticleBMC neuroscience2009

Expression of iron-related genes in human brain and brain tumors.

Milla M Hänninen, Joonas Haapasalo, Hannu Haapasalo, Robert E Fleming, Robert S Britton, Bruce R Bacon, Seppo Parkkila

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 93 citations in OpenAlex.

  1. Pooled it
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  7. Iron chelators: as therapeutic agents in diseases.Annals of medicine and surgery (2012) · 2024
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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

7 authors at 2 institutions in 3 countries.

Milla M HänninenInstitute of Medical Technology and School of Medicine, University of Tampere, Tampere University Hospital, Tampere, Finland. milla.hanninen@uta.fi
Joonas Haapasalo
Hannu Haapasalo
Robert E Fleming
Robert S Britton
Bruce R Bacon
Seppo Parkkila
Tampere University · FISaint Louis University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDefective iron homeostasis may be involved in the development of some diseases within the central nervous system. Although the expression of genes involved in normal iron balance has been intensively studied in other tissues, little is known about their expression in the brain. We investigated the mRNA levels of hepcidin (HAMP), HFE, neogenin (NEO1), transferrin receptor 1 (TFRC), transferrin receptor 2 (TFR2), and hemojuvelin (HFE2) in normal human brain, brain tumors, and astrocytoma cell lines. The specimens included 5 normal brain tissue samples, 4 meningiomas, one medulloblastoma, 3 oligodendrocytic gliomas, 2 oligoastrocytic gliomas, 8 astrocytic gliomas, and 3 astrocytoma cell lines.

resultsExcept for hemojuvelin, all genes studied had detectable levels of mRNA. In most tumor types, the pattern of gene expression was diverse. Notable findings include high expression of transferrin receptor 1 in the hippocampus and medulla oblongata compared to other brain regions, low expression of HFE in normal brain with elevated HFE expression in meningiomas, and absence of hepcidin mRNA in astrocytoma cell lines despite expression in normal brain and tumor specimens.

conclusionThese results indicate that several iron-related genes are expressed in normal brain, and that their expression may be dysregulated in brain tumors.

Indexed as

AdultAgedAged, 80 and overAntigens, CDAntimicrobial Cationic PeptidesAstrocytomaBrainBrain NeoplasmsCell Line, TumorFemaleGene Expression Regulation, NeoplasticGPI-Linked ProteinsHemochromatosis ProteinHepcidinsHistocompatibility Antigens Class IHumansAntigens, CDAntimicrobial Cationic PeptidesCD71 antigenGPI-Linked ProteinsHAMP protein, humanHemochromatosis ProteinHepcidinsHFE protein, humanHistocompatibility Antigens Class IHJV protein, humanMembrane ProteinsneogeninReceptors, TransferrinRNA, MessengerTFR2 protein, human

Identifiers

PMID19386095
PMCPMC2679039
OpenAlexW2097652402

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Registered trials

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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.