Evidence map›Paper›PMID 28144276›Full record

ArticleArchives of medical science : AMS2017

Leptin receptor expression during the progression of endometrial carcinoma is correlated with estrogen and progesterone receptors.

Luis Fernando Méndez-López, Angel Zavala-Pompa, Elva I Cortés-Gutiérrez, Ricardo M Cerda-Flores, Martha I Davila-Rodriguez

Open access · goldAbstract read
In one paragraph

Article in Archives of medical science : AMS, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 25% 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, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Revisiting Epithelial Carcinogenesis.International journal of molecular sciences · 2022
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  4. Review
  5. Article
  6. Article
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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

5 authors at 1 institution in 1 country.

Luis Fernando Méndez-LópezDivision of Genetics, Biomedical Research Center Northeast, Mexican Social Security Institute, Monterrey, México.
Angel Zavala-PompaMedicina Diagnóstica SA de CV, Monterrey, Mexico.
Elva I Cortés-GutiérrezDivision of Genetics, Biomedical Research Center Northeast, Mexican Social Security Institute, Monterrey, México.
Ricardo M Cerda-FloresSchool of Nursing, University of Nuevo Leon, Monterrey, México.
Martha I Davila-RodriguezDivision of Genetics, Biomedical Research Center Northeast, Mexican Social Security Institute, Monterrey, México.
Mexican Social Security Institute · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe hormone leptin, which is produced in the adipose tissue, may influence tumorigenesis directly via its receptor (Ob-R). Thus, a role for Ob-R in endometrial carcinogenesis has been proposed. However, most studies neither included samples of the entire histological progression of endometrial carcinoma nor examined Ob-R jointly with the estrogen and progesterone receptors (ER and PR, respectively). MATERIAL AND

methodsTo determine the fluctuations of Ob-R, ER, and PR during the histological progression of endometrial carcinoma, we assessed their expression via immunohistochemistry (IHC) in six histological types of endometrium (proliferative, secretory, nonatypical and atypical hyperplasia, and endometrioid and nonendometrioid endometrial carcinoma), in which we performed histopathological and digital scoring for the quantification of receptors.

resultsWe found that Ob-R expression was positively correlated with that of ER and PR (

conclusionsThese results indicate that Ob-R expression fluctuates during endometrial carcinogenesis in correlation with ER and PR, suggesting that Ob-R expression

Indexed as

endometrial carcinomaimmunohistochemistryOb-R

Identifiers

PMID28144276
PMCPMC5206378
OpenAlexW2589032265

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.