Evidence map›Paper›PMID 36806197›Full record

ArticleCell death discovery2023

A regulatory network controlling ovarian granulosa cell death.

Liu Yang, Xing Du, Siqi Wang, Chenggang Lin, Qiqi Li, Qifa Li

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.0field-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

11 citing papers in PubMed, 21 citations in OpenAlex.

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  11. miR-423 sponged by lncRNA NORHA inhibits granulosa cell apoptosis.Journal of animal science and biotechnology · 2023
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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

6 authors at 1 institution in 1 country.

Liu YangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Xing DuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Siqi WangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Chenggang LinCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Qiqi LiCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Qifa LiCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China. liqifa@njau.edu.cn.ORCID http://orcid.org/0000-0002-7985-3799
Nanjing Agricultural University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32072693
6 · The paper itself

Abstract

Follicular atresia triggered by granulosa cell (GC) apoptosis severely reduces female fertility and accelerates reproductive aging. GC apoptosis is a complex process regulated by multiple factors, regulatory axes, and signaling pathways. Here, we report a novel, small regulatory network involved in GC apoptosis and follicular atresia. miR-187, a miRNA down-regulated during follicular atresia in sows, maintains TGFBR2 mRNA stability in sow GCs by directly binding to its 5'-UTR. miR-187 activates the transforming growth factor-β (TGF-β) signaling pathway and suppresses GC apoptosis via TGFBR2 activation. NORHA, a pro-apoptotic lncRNA expressed in sow GCs, inhibits TGFBR2-mediated activation of the TGF-β signaling pathway by sponging miR-187. In contrast, NORFA, a functional lncRNA associated with sow follicular atresia and GC apoptosis, enhances miR-187 and TGFBR2 expression by inhibiting NORHA and activating NFIX. Our findings define a simple regulatory network that controls GC apoptosis and follicular atresia, providing new insights into the mechanisms of GC apoptosis, follicular atresia, and female fertility.

Identifiers

PMID36806197
PMCPMC9941584
OpenAlexW4321367851

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.