Evidence map›Paper›PMID 36583833›Full record

ReviewJournal of endocrinological investigation2023

Androgens in endometrial carcinoma: the killer or helper?

X Wu, K Zhang, X Zhong, X Huo, J Zhang, W Tian, X Yang, Y Zhang, Y Wang

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of endocrinological investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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  3. Review
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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 2 institutions in 1 country.

X WuDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.ORCID http://orcid.org/0000-0002-3793-5462
K ZhangDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
X ZhongDepartment of Gynecology and Obstetrics, Affiliated Hospital of Nantong University, Nantong City, China.
X HuoDepartment of Gynecology and Obstetrics, Affiliated Hospital of Nantong University, Nantong City, China.
J ZhangDepartment of Gynecology and Obstetrics, Affiliated Hospital of Nantong University, Nantong City, China.
W TianDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
X YangDepartment of Gynecology and Obstetrics, Affiliated Hospital of Nantong University, Nantong City, China. ntyxq169@126.com.
Y ZhangDepartment of Gynecology and Obstetrics, Affiliated Hospital of Nantong University, Nantong City, China. jsnt_zhangyuquan@163.com.
Y WangDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China. wangyingmei@tmu.edu.cn.
Nantong University · CNTianjin Medical University General Hospital · CN

Funding

National Natural Science Foundation of China 81572568The Youth Research grant of Nantong Commission of Health No. QB2021002Tianjin Municipal Science and Technology Bureau 20JCZDJC00330
6 · The paper itself

Abstract

purposeThe aim of this review is to discuss the role of androgens in the progression of endometrial carcinoma (EC) with particular focus on the different kinds of androgenic hormones, androgen receptor (AR) and intracrine androgen metabolism.

methodsA comprehensive literature search within PubMed was performed. Selected publications related to androgens and EC were reviewed.

resultsThere are different kinds of androgenic hormones, and different kinds of androgens may have different effects. Elevated androgens (especially testosterone) have been associated with an increased EC risk in postmenopausal women. 5α-reductases (5α-Reds) and 17β-hydroxysteroid dehydrogenase type 2 (17βHSD2) pathway may inhibit the progression of EC mediated by dihydrotestosterone (DHT), but aromatases stimulate further progression of EC. The most of studies accessing the prognostic value of AR have found that AR expression may be a favorable prognostic indicator.

conclusionAndrogens may have both oncogenic and tumor suppressive roles. Androgen-specific biases in metabolism and the expression of AR may contribute to the different prognosis of patients with EC.

Indexed as

AndrogensEndometrial NeoplasmsDihydrotestosteroneFemaleHumansReceptors, AndrogenTestosteroneAndrogensDihydrotestosteroneReceptors, AndrogenTestosteroneAndrogen receptorAndrogensEndometrial carcinomaMetabolismRisk–benefit

Identifiers

PMID36583833
PMCPMC9938034
OpenAlexW4313299805

What OpenQuestion holds

Textmetadata
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.