Evidence map›Paper›PMID 30130469›Full record

ReviewAnnual review of nutrition2018

Iron and Cancer.

Suzy V Torti, David H Manz, Bibbin T Paul, Nicole Blanchette-Farra, Frank M Torti

Abstract readReview
In one paragraph

Review in Annual review of nutrition, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 253 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
253citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

253 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Heavy metals in biological samples of cancer patients: a systematic literature review.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2024
    Pooled it
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193 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

5 authors.

Suzy V TortiDepartment of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut 06030, USA; email: storti@uchc.edu.
David H ManzDepartment of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut 06030, USA; email: storti@uchc.edu.
Bibbin T PaulDepartment of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut 06030, USA; email: storti@uchc.edu.
Nicole Blanchette-FarraDepartment of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut 06030, USA; email: storti@uchc.edu.
Frank M TortiDepartment of Medicine, University of Connecticut Health Center, Farmington, Connecticut 06030, USA.

Funding

Skeletal, Craniofacial and Oral Biology Training GrantT90DE021989 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MINA, MINA · 2011 to 2022
$4.5M
Iron, Ferroptosis and Ovarian CancerR01CA188025 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI TORTI, SUZY V · 2014 to 2024
$3.9M
Ferroportin and Iron HomeostasisR01CA171101 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI TORTI, FRANK M. · 2012 to 2016
$1.7M
Role of Ferroportin in reducing Prostate Cancer MetastasisF30DE026380 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MANZ, DAVID H · 2016 to 2021
$207k
NCI NIH HHS R01 CA171101NCI NIH HHS R01 CA188025NIDCR NIH HHS F30 DE026380NIDCR NIH HHS T90 DE021989
6 · The paper itself

Abstract

This review explores the multifaceted role that iron has in cancer biology. Epidemiological studies have demonstrated an association between excess iron and increased cancer incidence and risk, while experimental studies have implicated iron in cancer initiation, tumor growth, and metastasis. The roles of iron in proliferation, metabolism, and metastasis underpin the association of iron with tumor growth and progression. Cancer cells exhibit an iron-seeking phenotype achieved through dysregulation of iron metabolic proteins. These changes are mediated, at least in part, by oncogenes and tumor suppressors. The dependence of cancer cells on iron has implications in a number of cell death pathways, including ferroptosis, an iron-dependent form of cell death. Uniquely, both iron excess and iron depletion can be utilized in anticancer therapies. Investigating the efficacy of these therapeutic approaches is an area of active research that promises substantial clinical impact.

Indexed as

HumansIronIron OverloadNeoplasmsIroncancercarcinogenesiscell deathiron

Identifiers

PMID30130469
PMCPMC8118195

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.