Evidence map›Paper›PMID 12890810›Full record

ArticleJournal of clinical pathology2003

Insulin-like growth factor system gene expression in women with type 2 diabetes and breast cancer.

E Nardon, I Buda, G Stanta, E Buratti, M Fonda, L Cattin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical pathology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Molecular characterisation of breast cancer patients at high and low recurrence risk.Virchows Archiv : an international journal of pathology · 2008
    Article
  4. Article
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 3 institutions in 1 country.

E NardonDepartment of Clinical, Morphological and Technological Sciences, University of Trieste, Italy.
I Buda
G Stanta
E Buratti
M Fonda
L Cattin
University of Trieste · ITInternational Centre for Genetic Engineering and Biotechnology · ITOspedale di Cattinara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsA twofold increased risk for breast cancer has been reported recently for women with late onset diabetes. Most studies showed that there were differences in serum concentrations of insulin-like growth factors and related proteins between women with and without diabetes who have breast cancer. This study investigated the expression of these markers at the cellular level in a cohort of women with and without type 2 diabetes who underwent biopsy because of a breast lump.

methodsRelative quantitative analysis of specific mRNA sequences was performed after extraction and reverse transcription polymerase chain reaction amplification from formalin fixed and paraffin wax embedded tissues. Sixty seven breast surgical specimens from women with and without diabetes who did not have cancer and from women with and without diabetes who did have cancer were studied for insulin-like growth factor I (IGF-I), the IGF-I receptor (IGF-IR), insulin-like growth factor binding protein 3 (IGFBP-3), and oestrogen receptor 1 gene expression.

resultsThe expression of IGF-I and IGF-IR was significantly lower in the cancer groups, whereas there was no significant difference for IGFBP-3 between women with and without cancer. Moreover, there was a good correlation between the expression of IGF-I and IGF-IR in women without cancer: this link was still present in breast tissue from patients with diabetes and cancer, whereas it was lost in patients without diabetes but with cancer.

conclusionsThese differences in IGF-I/IGF-IR expression could contribute to the increased risk for breast cancer in women with type 2 diabetes.

Indexed as

AdolescentAdultAgedAged, 80 and overAnalysis of VarianceBreast NeoplasmsCase-Control StudiesDiabetes Mellitus, Type 2FemaleGene ExpressionHumansImmunohistochemistryInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor IMiddle AgedReceptor, IGF Type 1Insulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor IReceptor, IGF Type 1Receptors, EstrogenRNA, Messenger

Identifiers

PMID12890810
PMCPMC1770044
OpenAlexW2170761727

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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.