Evidence map›Paper›PMID 27579887›Full record

ArticleCell cycle (Georgetown, Tex.)2016

Hmgn5 functions downstream of Hoxa10 to regulate uterine decidualization in mice.

Dang-Dang Li, Shu-Yi Zhao, Zhan-Qing Yang, Cui-Cui Duan, Chuan-Hui Guo, Hong-Liang Zhang, Shuang Geng, Zhan-Peng Yue, Bin Guo

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. High Mobility Group Proteins in Sepsis.Frontiers in immunology · 2022
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

9 authors at 2 institutions in 1 country.

Dang-Dang Lia College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Shu-Yi Zhaoa College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Zhan-Qing Yanga College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Cui-Cui Duanb Institute of Agro-food Technology , Jilin Academy of Agricultural Sciences , Changchun , P. R. China.
Chuan-Hui Guoa College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Hong-Liang Zhanga College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Shuang Genga College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Zhan-Peng Yuea College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Bin Guoa College of Veterinary Medicine , Jilin University , Changchun , P. R. China.
Jilin University · CNJilin Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although Hmgn5 is involved in the regulation of cellular proliferation and differentiation, its physiological function during decidualization is still unknown. Here we showed that Hmgn5 was highly expressed in the decidual cells. Silencing of Hmgn5 expression by specific siRNA reduced the proliferation of uterine stromal cells and expression of Ccnd3 and Cdk4 in the absence or presence of estrogen and progesterone, whereas overexpression of Hmgn5 exhibited the opposite effects. Simultaneously, Hmgn5 might induce the expression of Prl8a2 and Prl3c1 which were 2 well-known differentiation markers for decidualization. In the uterine stromal cells, cAMP analog 8-Br-cAMP and progesterone could up-regulate the expression of Hmgn5, but the up-regulation was impeded by H89 and RU486, respectively. Attenuation of Hmgn5 expression could block the differentiation of uterine stromal cells in response to cAMP and progesterone. Further studies found that regulation of cAMP and progesterone on Hmgn5 expression was mediated by Hoxa10. During in vitro decidualization, knockdown of Hmgn5 could abrogate Hoxa10-induced upregulation of Prl8a2 and Prl3c1, while overexpression of Hmgn5 reversed the inhibitory effects of Hoxa10 siRNA on the expression of Prl8a2 and Prl3c1. In the stromal cells undergoing decidualization, Hmgn5 might act downstream of Hoxa10 to regulate the expression of Cox-2, Vegf and Mmp2. Collectively, Hmgn5 may play an important role during mouse decidualization.

Indexed as

AnimalsCell DifferentiationCell ProliferationCyclic AMPCyclooxygenase 2DeciduaFemaleHMGN ProteinsHomeobox A10 ProteinsHomeodomain ProteinsIn Situ HybridizationMatrix Metalloproteinase 2MicePregnancyProgesteroneReal-Time Polymerase Chain ReactionCyclic AMPCyclooxygenase 2Hmgn5 protein, mouseHMGN ProteinsHomeobox A10 ProteinsHomeodomain ProteinsHoxa10 protein, mouseMatrix Metalloproteinase 2ProgesteroneRNA, MessengerVascular Endothelial Growth Factor AdecidualizationHmgn5mousestromal celluterus

Identifiers

PMID27579887
PMCPMC5053560
OpenAlexW2513134584

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.