Evidence map›Paper›PMID 27882941›Full record

ArticleCell death & disease2016

TGF-β signaling controls FSHR signaling-reduced ovarian granulosa cell apoptosis through the SMAD4/miR-143 axis.

Xing Du, Lifan Zhang, Xinyu Li, Zengxiang Pan, Honglin Liu, Qifa Li

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

63 citing papers in PubMed, 130 citations in OpenAlex.

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  13. Inhibition ofCells · 2024
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  14. Review
  15. miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis.Journal of animal science and biotechnology · 2023
    Article
  16. Article
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3 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Xing DuCollege of Animal Science and Technology, Department of Animal Genetics, Breeding and Reproduction, Nanjing Agricultural University, Nanjing, China.
Lifan ZhangCollege of Animal Science and Technology, Department of Animal Genetics, Breeding and Reproduction, Nanjing Agricultural University, Nanjing, China.
Xinyu LiCollege of Animal Science and Technology, Department of Animal Genetics, Breeding and Reproduction, Nanjing Agricultural University, Nanjing, China.
Zengxiang PanCollege of Animal Science and Technology, Department of Animal Genetics, Breeding and Reproduction, Nanjing Agricultural University, Nanjing, China.
Honglin LiuCollege of Animal Science and Technology, Department of Animal Genetics, Breeding and Reproduction, Nanjing Agricultural University, Nanjing, China.
Qifa LiCollege of Animal Science and Technology, Department of Animal Genetics, Breeding and Reproduction, Nanjing Agricultural University, Nanjing, China.
Nanjing Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Follicle-stimulating hormone receptor (FSHR) and its intracellular signaling control mammalian follicular development and female infertility. Our previous study showed that FSHR is downregulated during follicular atresia of porcine ovaries. However, its role and regulation in follicular atresia remain unclear. Here, we showed that FSHR knockdown induced porcine granulosa cell (pGC) apoptosis and follicular atresia, and attenuated the levels of intracellular signaling molecules such as PKA, AKT and p-AKT. FSHR was identified as a target of miR-143, a microRNA that was upregulated during porcine follicular atresia. miR-143 enhanced pGC apoptosis by targeting FSHR, and reduced the levels of intracellular signaling molecules. SMAD4, the final molecule in transforming growth factor (TGF)-β signaling, bound to the promoter and induced significant downregulation of miR-143 in vitro and in vivo. Activated TGF-β signaling rescued miR-143-reduced FSHR and intracellular signaling molecules, and miR-143-induced pGC apoptosis. Overall, our findings offer evidence to explain how TGF-β signaling influences and FSHR signaling for regulation of pGC apoptosis and follicular atresia by a specific microRNA, miR-143.

Indexed as

ApoptosisSignal TransductionAnimalsBase SequenceFemaleFollicular AtresiaGene Knockdown TechniquesGranulosa CellsMicroRNAsModels, BiologicalPromoter Regions, GeneticProtein BindingReceptors, FSHSmad4 ProteinSus scrofaTransforming Growth Factor betaMicroRNAsReceptors, FSHSmad4 ProteinTransforming Growth Factor beta

Identifiers

PMID27882941
PMCPMC5260897
OpenAlexW2550547921

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.