Evidence map›Paper›PMID 19141577›Full record

ArticleThe Journal of clinical endocrinology and metabolism2009

Transcriptional profiling with a pathway-oriented analysis identifies dysregulated molecular phenotypes in the endometrium of patients with polycystic ovary syndrome.

Jin Yeong Kim, Haengseok Song, Hyunjoo Kim, Hee Jung Kang, Jin Hyun Jun, Sung Ran Hong, Mi Kyoung Koong, In Sun Kim

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Integrative Multi-omics Analysis for Prioritization of Candidate Genes in Polycystic Ovary Syndrome.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Article
  6. Journal of advanced research · 2022
    Article
  7. Review
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  12. Article
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  15. Immunometabolism, pregnancy, and nutrition.Seminars in immunopathology · 2018
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Jin Yeong KimDepartment of Obstetrics andGynecology, Cheil General Hospital and Women's Healthcare Center, Kwangdong University College of Medicine, Seoul, Korea.
Haengseok Song
Hyunjoo Kim
Hee Jung Kang
Jin Hyun Jun
Sung Ran Hong
Mi Kyoung Koong
In Sun Kim
Cheil General Hospital and Women's Healthcare Center · KRKorea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextPolycystic ovary syndrome (PCOS) is a common endocrine disorder characterized by chronic oligo/anovulation, hyperandrogenemia, infertility, and metabolic alterations related to insulin resistance. These abnormalities in PCOS may have complex effects on pathophysiology of the endometrium, contributing to infertility and endometrial disorders.

objectiveThe objective of this study was to examine dysregulated signaling pathways in the endometrium of patients with PCOS (PCOSE) by analyzing expression profiles with a pathway-oriented method.

designMicroarrays, RT-PCR, laser capture microdissection, and immunohistochemistry were performed with endometrial tissues.

settingThis study was performed at a university hospital laboratory. PATIENTS: This study comprised 12 regularly cycling women and 12 PCOS patients.

main outcome measureDysregulated signaling pathways in PCOSE were identified as a gene set.

resultsHierarchical clustering revealed distinct expression profiles for PCOSE and the endometrium of normal cycling women. Gene sets associated with androgen signaling were not enriched in PCOSE, although they affect ovarian physiology of PCOS patients. Several biological pathways including cell cycle, apoptosis, glycolysis, and integrin-Rho-cytoskeleton network were aberrantly down-regulated in PCOSE. Expression of genes constituting these gene sets enriched in normal cycling women was systemically down-regulated in PCOSE. Laser capture microdissection-coupled real-time RT-PCR and immunohistochemistry further demonstrated that cell proliferation in the stroma, but not the epithelium, is significantly reduced in PCOSE.

conclusionsSystemic down-regulation of various signaling pathways in PCOSE with extremely prolonged proliferative phase provides insight into the abnormal phenotypes that reflect pathophysiology of PCOS in the endometrium, possibly leading to increased risks of endometrial disorders.

Indexed as

Gene Expression ProfilingTranscription, GeneticAdultAndrogensDehydroepiandrosterone SulfateEndometriumEstradiolEstrogensFemaleFollicle Stimulating HormoneHumansLuteinizing HormoneMenstrual CycleOligonucleotide Array Sequence AnalysisPhenotypePolycystic Ovary SyndromeAndrogensDehydroepiandrosterone SulfateEstradiolEstrogensFollicle Stimulating HormoneLuteinizing HormoneRNATestosterone

Identifiers

PMID19141577
PMCPMC2682468
OpenAlexW2044185104

What OpenQuestion holds

Textmetadata
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.