Evidence map›Paper›PMID 25392569›Full record

ArticleActa histochemica et cytochemica2014

A Histopathological Study of Multi-hormone Producing Proliferative Lesions in Estrogen-induced Rat Pituitary Prolactinoma.

Susumu Takekoshi, Yuzo Yasui, Chie Inomoto, Kanae Kitatani, Naoya Nakamura, Robert Yoshiyuki Osamura

Open access · diamondAbstract read
In one paragraph

Article in Acta histochemica et cytochemica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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  5. Acta histochemica et cytochemica · 2017
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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 2 institutions in 1 country.

Susumu TakekoshiDepartment of Cell Biology, Division of Host Defense Mechanism, Tokai University School of Medicine , 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
Yuzo YasuiDepartment of Cell Biology, Division of Host Defense Mechanism, Tokai University School of Medicine , 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
Chie InomotoDepartment of Pathology, Tokai University School of Medicine , 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
Kanae KitataniDepartment of Cell Biology, Division of Host Defense Mechanism, Tokai University School of Medicine , 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
Naoya NakamuraDepartment of Pathology, Tokai University School of Medicine , 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
Robert Yoshiyuki OsamuraCenter for Diagnostic Pathology, International University of Health and Welfare Mita Hospital , 1-4-3 Mita, Minato-ku, Tokyo 108-8239, Japan.
Tokai University · JPMita Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rats with estrogen-induced prolactin-producing pituitary adenoma (E2-PRLoma) have been employed as an animal model of human PRL-producing pituitary adenoma in a large number of studies. Presently, we found that long-term administration of estrogen to SD rats resulted in the development of E2-PRLomas, some of which included multi-hormone producing nodules. We herein report results of histopathological analyses of these lesions. PRLoma models were created in female SD rats by 22 weeks or longer administration of a controlled-release preparation of estradiol at a dose of 10 mg/kg/2 weeks. Ten of the 11 PRLoma model rats had proliferative nodular lesions composed of large eosinophilic cells like gonadotrophs inside the PRLoma. These lesions were positive for PRL, TSHβ, and α subunits and were negative for GH, LHβ, ACTH, and S-100. Double immunostaining revealed that these large eosinophilic cells showed coexpression of PRL and TSHβ, PRL and α subunits, and TSHβ and α subunits. Those results clarified that long-term estrogen administration to female SD rats induced multi-hormone producing neoplastic pituitary nodules that expressed PRL, TSHβ, and α subunits. We studied these neoplastic nodules obtained by laser microdissection to acquire findings similar to those of the immuno-histochemical analysis. We consider that this animal model is useful for pathogenesis analyses and therapeutic agent development concerning human multi-hormone producing pituitary adenomas.

Indexed as

estrogenlaser capture microdissectionmulti-hormone producing adenomaprolactinoma

Identifiers

PMID25392569
PMCPMC4164703
OpenAlexW2007421933

What OpenQuestion holds

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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.