Evidence map›Paper›PMID 37289566›Full record

ReviewMolecular human reproduction2023

Progesterone signaling in the regulation of luteal steroidogenesis.

Kayhan Yakin, Francesko Hela, Ozgur Oktem

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular human reproduction, 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
5.2field-weighted citation impact, top 5% 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, 15 citations in OpenAlex.

  1. Trial
  2. The Role of β-Core Fragment hCG in Embryo Implantation and Early Pregnancy.International journal of molecular sciences · 2025
    Article
  3. Article
  4. Article
  5. Role of circadian clock in female embryo implantation.Frontiers in cell and developmental biology · 2025
    Review
  6. Article
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

3 authors at 2 institutions in 2 countries.

Kayhan YakinGraduate School of Health Sciences, Koç University, Istanbul, Turkey.ORCID 0000-0002-8987-6062
Francesko HelaGraduate School of Health Sciences, Koç University, Istanbul, Turkey.ORCID 0000-0002-9977-1221
Ozgur OktemGraduate School of Health Sciences, Koç University, Istanbul, Turkey.ORCID 0000-0003-1966-3886
Koç University · TRJoslin Diabetes Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The corpus luteum is the major source of progesterone, the essential hormone for female reproductive function. While progesterone activity has been the subject of extensive research for decades, characterization of non-canonical progesterone receptor/signaling pathways provided a new perspective for understanding the complex signal transduction mechanisms exploited by the progesterone hormone. Deciphering these mechanisms has significant implications in the management of luteal phase disorders and early pregnancy complications. The purpose of this review is to highlight the complex mechanisms through which progesterone-induced signaling mediates luteal granulosa cell activity in the corpus luteum. Here, we review the literature and discuss the up-to-date evidence on how paracrine and autocrine effects of progesterone regulate luteal steroidogenic activity. We also review the limitations of the published data and highlight future research priorities.

Indexed as

Corpus LuteumProgesteroneFemaleGranulosa CellsHormonesHumansPregnancySignal TransductionHormonesProgesteroneangiogenesisapoptosischolesterolcorpus luteumgranulosa cellluteotrophinpregnancyprogesteronesteroidogenesis

Identifiers

PMID37289566
PMCPMC10631818
OpenAlexW4379878856

What Socratic 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 Socratic graph.