Evidence map›Paper›PMID 37924640›Full record

ArticleEndocrine connections2023

17β-hydroxysteroid dehydrogenase type 1 improves survival in serous epithelial ovarian tumors.

Enrique Pedernera, Flavia Morales-Vásquez, María J Gómora, Miguel A Almaraz, Esteban Mena, Delia Pérez-Montiel, Elizabeth Rendon, Horacio López-Basave, Juan Maldonado-Cubas, Carmen Méndez

Open access · goldAbstract read
In one paragraph

Article in Endocrine connections, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.6field-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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Review
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

10 authors at 4 institutions in 3 countries.

Enrique PederneraUniversidad Nacional Autónoma de México, Facultad de Medicina, Departamento de Embriología y Genética, Ciudad de México, México.
Flavia Morales-VásquezInstituto Nacional de Cancerología, Ciudad de México, México.
María J GómoraUniversidad Nacional Autónoma de México, Facultad de Medicina, Departamento de Embriología y Genética, Ciudad de México, México.
Miguel A AlmarazUniversidad Nacional Autónoma de México, Facultad de Medicina, Departamento de Embriología y Genética, Ciudad de México, México.
Esteban MenaUniversidad Nacional Autónoma de México, Facultad de Medicina, Secretaría General, Ciudad de México, México.
Delia Pérez-MontielInstituto Nacional de Cancerología, Ciudad de México, México.
Elizabeth RendonHospital Militar de Especialidades de la Mujer y Neonatología. Ciudad de México, México.
Horacio López-BasaveInstituto Nacional de Cancerología, Ciudad de México, México.
Juan Maldonado-CubasUniversidad La Salle, Posgrado de la Facultad de Ciencias Químicas, Ciudad de México, México.
Carmen MéndezUniversidad Nacional Autónoma de México, Facultad de Medicina, Departamento de Embriología y Genética, Ciudad de México, México.ORCID 0000-0002-8342-3927
Universidad Nacional Autónoma de México · MXInstituto Nacional de Cancerología · MXUniversidad La Salle · BOHospital Militar Central · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of ovarian cancer has been epidemiologically related to female reproductive events and hormone replacement therapy after menopause. This highlights the importance of evaluating the role of sexual steroid hormones in ovarian cancer by the expression of enzymes related to steroid hormone biosynthesis in the tumor cells. This study was aimed to evaluate the presence of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1), aromatase and estrogen receptor alpha (ERα) in the tumor cells and their association with the overall survival in 111 patients diagnosed with primary ovarian tumors. Positive immunoreactivity for 17β-HSD1 was observed in 74% of the tumors. In the same samples, aromatase and ERα revealed 66% and 47% positivity, respectively. No association was observed of 17β-HSD1 expression with the histological subtypes and clinical stages of the tumor. The overall survival of patients was improved in 17β-HSD1-positive group in Kaplan-Meier analysis (P = 0.028), and 17β-HSD1 expression had a protective effect from multivariate proportional regression evaluation (HR = 0.44; 95% CI 0.24-0.9; P = 0.040). The improved survival was observed in serous epithelial tumors but not in nonserous ovarian tumors. The expression of 17β-HSD1 in the cells of the serous epithelial ovarian tumors was associated with an improved overall survival, whereas aromatase and ERα were not related to a better survival. The evaluation of hazard risk factors demonstrated that age and clinical stage showed worse prognosis, and 17β-HSD1 expression displayed a protective effect with a better survival outcome in patients of epithelial ovarian tumors.

Indexed as

17β-hydroxysteroid dehydrogenasearomataseepithelial ovarian tumorestrogen receptorovarian canceroverall survival

Identifiers

PMID37924640
PMCPMC10762561
OpenAlexW4388097398

What OpenQuestion holds

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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.