Evidence map›Paper›PMID 32655839›Full record

ArticleOncotarget2020

IGF-1 and hyperglycaemia-induced FOXA1 and IGFBP-2 affect epithelial to mesenchymal transition in prostate epithelial cells.

Rehanna Mansor, Jeff Holly, Rachel Barker, Kalina Biernacka, Hanna Zielinska, Anthony Koupparis, Edward Rowe, Jon Oxley, Alex Sewell, Richard M Martin and 3 more

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  8. Review
  9. Review
  10. FOXA1 in prostate cancer.Asian journal of andrology
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 3 countries.

Rehanna MansorIGFs and Metabolic Endocrinology Group, Bristol Medical School, Translational Health Sciences, University of Bristol, Southmead Hospital, Bristol, UK.
Jeff HollyIGFs and Metabolic Endocrinology Group, Bristol Medical School, Translational Health Sciences, University of Bristol, Southmead Hospital, Bristol, UK.
Rachel BarkerIGFs and Metabolic Endocrinology Group, Bristol Medical School, Translational Health Sciences, University of Bristol, Southmead Hospital, Bristol, UK.
Kalina BiernackaIGFs and Metabolic Endocrinology Group, Bristol Medical School, Translational Health Sciences, University of Bristol, Southmead Hospital, Bristol, UK.
Hanna ZielinskaIGFs and Metabolic Endocrinology Group, Bristol Medical School, Translational Health Sciences, University of Bristol, Southmead Hospital, Bristol, UK.
Anthony KoupparisDepartment of Urology, Bristol Urological Institute, Southmead Hospital, Bristol, UK.
Edward RoweDepartment of Urology, Bristol Urological Institute, Southmead Hospital, Bristol, UK.
Jon OxleyDepartment of Cellular Pathology, North Bristol NHS Trust, Southmead Hospital, Bristol, UK.
Alex SewellDepartment of Cellular Pathology, North Bristol NHS Trust, Southmead Hospital, Bristol, UK.
Richard M MartinNIHR Biomedical Research Centre, Level 3, University Hospitals Bristol Education Centre, Bristol, UK.
Athene LaneNIHR Biomedical Research Centre, Level 3, University Hospitals Bristol Education Centre, Bristol, UK.
Lucy Hackshaw-McGeaghNIHR Biomedical Research Centre, Level 3, University Hospitals Bristol Education Centre, Bristol, UK.
Claire PerksIGFs and Metabolic Endocrinology Group, Bristol Medical School, Translational Health Sciences, University of Bristol, Southmead Hospital, Bristol, UK.
University of Bristol · GBNIHR Bristol Biomedical Research Centre · GBNorth Bristol NHS Trust · GBSouthmead Hospital · GB

Funding

Cancer Research UK 19169
6 · The paper itself

Abstract

Localized prostate cancer (PCa) is a manageable disease but for most men with metastatic disease, it is often fatal. A western diet has been linked with PCa progression and hyperglycaemia has been associated with the risk of lethal and fatal prostate cancer. Using PCa cell lines, we examined the impact of IGF-I and glucose on markers of epithelial-to-mesenchymal transition (EMT), migration and invasion. We examined the underlying mechanisms using cell lines and tumour tissue samples. IGF-I had differential effects on the process of EMT: inhibiting in normal and promoting in cancer cells, whereas hyperglycamia alone had a stimulatory effect in both. These effects were independent of IGF and in both cases, hyperglycaemia induced an increase IGFBP-2(tumour promoter) and FOXA1. A positive correlation existed between levels of IGFBP-2 and FOXA1 in benign and cancerous prostate tissue samples and

Indexed as

EMTFOXA1hyperglycaemiaIGFBP-2prostate cancer

Identifiers

PMID32655839
PMCPMC7335671
OpenAlexW3039445629

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.