Evidence map›Paper›PMID 18715471›Full record

ArticleInternational journal of experimental pathology2008

Malignant lesions in the ventral prostate of alloxan-induced diabetic rats.

Daniele Lisboa Ribeiro, Silvio Fernando Guideti Marques, Sandra Alberti, César Tadeu Spadella, Antônio José Manzato, Sebastião Roberto Taboga, Nishtman Dizeyi, Per-Anders Abrahamsson, Rejane Maira Góes

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In one paragraph

Article in International journal of experimental pathology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 30 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

9 authors at 3 institutions in 2 countries.

Daniele Lisboa RibeiroDepartment of Cell Biology, State University of Campinas, Unicamp, Campinas, Brazil.
Silvio Fernando Guideti Marques
Sandra Alberti
César Tadeu Spadella
Antônio José Manzato
Sebastião Roberto Taboga
Nishtman Dizeyi
Per-Anders Abrahamsson
Rejane Maira Góes
Universidade Estadual Paulista (Unesp) · BRLund University · SEUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to evaluate the changes caused by chronic diabetes in the rat ventral prostate and to establish a correlation between diabetes and the development of prostatic lesions. Male rats received alloxan (42 mg/kg b.w.) to induce diabetes. Ninety days after diabetes diagnosis, animals were sacrificed and the ventral prostate was removed and prepared for general and immunohistochemical analyses. The total area showing different types of lesions was estimated. Diabetes led to a decrease in the body and prostatic weights, as well as in testosterone levels. The prostate morphology and stereology showed high variation in the diabetic group. Some animals had light changes; the great majority had an intense epithelial atrophy; and other rats showed premalignant and malignant lesions in the prostate. Such epithelial atrophy was, in some samples, combined with chronic inflammation, similar to proliferative inflammatory atrophy (PIA). The diabetic group also presented high incidence of prostatitis, adenocarcinoma and prostatic intra-epithelial neoplasia (PIN). Samples with adenocarcinoma had poorly differentiated acini with high levels of cellular proliferation and nuclear atypia. These lesions exhibited an invasive feature showing Bcl-2-positive cells and interruptions in the basement membrane. An association of PIA, PIN and adenocarcinoma was detected in one sample. Reduced androgen levels have a synergic effect to insulin dysfunction promoting negative effects in the rat prostate. Diabetic individuals had a high incidence of prostatitis, and this inflammation could stimulate the incidence of other forms of prostatic pathology.

Indexed as

AdenocarcinomaAnimalsBiomarkers, TumorDiabetes Mellitus, ExperimentalImmunohistochemistryMaleProstateProstatic HyperplasiaProstatic Intraepithelial NeoplasiaProstatic NeoplasmsProstatitisProto-Oncogene Proteins c-bcl-2RatsRats, WistarTenascinTestosteroneBiomarkers, TumorProto-Oncogene Proteins c-bcl-2TenascinTestosterone

Identifiers

PMID18715471
PMCPMC2525783
OpenAlexW2165417813

What OpenQuestion holds

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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.