Evidence map›Paper›PMID 28244645›Full record

ArticleJournal of cellular and molecular medicine2017

Obesity and metabolic dysfunction severely influence prostate cell function: role of insulin and IGF1.

Fernando L-López, André Sarmento-Cabral, Vicente Herrero-Aguayo, Manuel D Gahete, Justo P Castaño, Raúl M Luque

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Nutrition, GH/IGF-1 signaling, and cancer.Endocrine-related cancer · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Article
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  11. Observational
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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

6 authors at 4 institutions in 1 country.

Fernando L-LópezMaimónides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
André Sarmento-CabralMaimónides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Vicente Herrero-AguayoMaimónides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Manuel D GaheteMaimónides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Justo P CastañoMaimónides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Raúl M LuqueMaimónides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain.
Hospital Universitario Reina Sofía · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESSpanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition · ESUniversity of Córdoba · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is a major health problem that courses with severe comorbidities and a drastic impairment of homeostasis and function of several organs, including the prostate gland (PG). The endocrine-metabolic regulatory axis comprising growth hormone (GH), insulin and IGF1, which is drastically altered under extreme metabolic conditions such as obesity, also plays relevant roles in the development, modulation and homeostasis of the PG. However, its implication in the pathophysiological interplay between obesity and prostate function is still to be elucidated. To explore this association, we used a high fat-diet obese mouse model, as well as in vitro primary cultures of normal-mouse PG cells and human prostate cancer cell lines. This approach revealed that most of the components of the GH/insulin/IGF1 regulatory axis are present in PGs, where their expression pattern is altered under obesity conditions and after an acute insulin treatment (e.g. Igfbp3), which might have some pathophysiological implications. Moreover, our results demonstrate, for the first time, that the PG becomes severely insulin resistant under diet-induced obesity in mice. Finally, use of in vitro approaches served to confirm and expand the conception that insulin and IGF1 play a direct, relevant role in the control of normal and pathological PG cell function. Altogether, these results uncover a fine, germane crosstalk between the endocrine-metabolic status and the development and homeostasis of the PG, wherein key components of the GH, insulin and IGF1 axes could play a relevant pathophysiological role.

Indexed as

AnimalsCell Line, TumorDiet, High-FatGrowth HormoneHumansInsulinInsulin-Like Growth Factor IInsulin ResistanceMaleMice, Inbred C57BLObesityProstateProstatic NeoplasmsRNA, MessengerSignal TransductionGrowth HormoneInsulinInsulin-Like Growth Factor IRNA, MessengerIGF1insulinobesityprostateprostate cancer

Identifiers

PMID28244645
PMCPMC5571563
OpenAlexW2593674951

What OpenQuestion holds

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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.