Evidence map›Paper›PMID 29391539›Full record

ReviewExperimental & molecular medicine2018

Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications.

Driton Vela, Zana Vela-Gaxha

Open access · goldAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

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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

2 authors.

Driton VelaDepartment of Physiology, Faculty of Medicine, University of Prishtina, Prishtina, Kosova, Albania.
Zana Vela-GaxhaDepartment of Histology and Pathology, Faculty of Medicine, University of Prishtina, Prishtina, Kosova, Albania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepcidin is a crucial peptide for regulating cellular iron efflux. Because iron is essential for cell survival, especially for highly active cells, such as tumor cells, it is imperative to understand how tumor cells manipulate hepcidin expression for their own metabolic needs. Studies suggest that hepcidin expression and regulation in tumor cells show important differences in comparison with those in non-tumorous cells. These differences should be investigated to develop new strategies to fight cancer cells. Manipulating hepcidin expression to starve cancer cells for iron may prove to be a new therapy in the anticancer arsenal.

Indexed as

Disease SusceptibilityGene Expression RegulationAnimalsBiomarkersDrug DiscoveryHepcidinsHumansInflammationIronMolecular Targeted TherapyNeoplasmsProtein BindingProtein IsoformsProtein TransportSignal TransductionBiomarkersHepcidinsIronProtein Isoforms

Identifiers

PMID29391539
PMCPMC5903825
OpenAlexW2785661688

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.