Evidence map›Paper›PMID 39317806›Full record

ArticleFunctional & integrative genomics2024

Transcription factor YY1 adversely governs ovarian granulosa cell growth in PCOS by transcription activation-mediated CDKN1C upregulation.

Shitao Dong, Youbin Liu, Zhimin Yang

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Article in Functional & integrative genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

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4 · The record

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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.

Shitao DongDepartment of Reproductve Medical, Affiliated Hospital of Zunyi Medical University, No. 149, Dalian Road, Huichuan Distyrict, Zunyi, 563000, China.
Youbin LiuDepartment of Reproductve Medical, Affiliated Hospital of Zunyi Medical University, No. 149, Dalian Road, Huichuan Distyrict, Zunyi, 563000, China.
Zhimin YangDepartment of Reproductve Medical, Affiliated Hospital of Zunyi Medical University, No. 149, Dalian Road, Huichuan Distyrict, Zunyi, 563000, China. dsthzy123@126.com.

Funding

Effect of Different Doses of Tributyltin Interference on Embryo Loss Rate in Polycystic Syndrome Pregnancy Model Mice Zunshi Kehe HZ Zi (2022) No. 246
6 · The paper itself

Abstract

backgroundPolycystic ovary syndrome (PCOS) is a common endocrine and metabolic disease in women of childbearing age, making it imperative to explore more biomarkers for PCOS. Furthermore, previous studies have reported that cyclin dependent kinase inhibitor 1 C (CDKN1C) might be associated with PCOS progression. However, the molecular mechanism of CDKN1C involved in PCOS is poorly defined.

methodsCDKN1C and Yin-Yang-1 (YY1) expression levels were determined using real-time quantitative polymerase chain reaction (RT-qPCR) and Western blot assay. Cell viability, proliferation, cell cycle progression, and cell apoptosis were analyzed using 3-(4, 5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2-H-tetrazolium bromide (MTT), 5-ethynyl-2'-deoxyuridine (EdU), and flow cytometry assays. Caspase 3 activity was examined using a commercial kit. Binding between YY1 and CDKN1C promoter was predicted by JASPAR and verified using Chromatin immunoprecipitation (ChIP) and dual-luciferase reporter assays.

resultsCDKN1C and YY1 were highly expressed in PCOS granulosa cells (GCs). Furthermore, CDKN1C silencing could promote cell proliferation and cell cycle process and repress cell apoptosis in human ovarian granulosa cell line KGN cells. For mechanistic analysis, YY1 is directly bound to the promoter of CDKN1C and transcriptional-regulated CDKN1C expression.

conclusionYY1-activated CDKN1C might block KGN cell proliferation and induce cell apoptosis, providing a possible therapeutic target for PCOS treatment.

Indexed as

ApoptosisCell ProliferationCyclin-Dependent Kinase Inhibitor p57Granulosa CellsPolycystic Ovary SyndromeTranscriptional ActivationUp-RegulationYY1 Transcription FactorAdultFemaleHumansPromoter Regions, GeneticCDKN1C protein, humanCyclin-Dependent Kinase Inhibitor p57YY1 protein, humanYY1 Transcription FactorCDKN1CKGN cellsPCOSProliferationYY1

Identifiers

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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.