Evidence map›Paper›PMID 25973037›Full record

ArticleInternational journal of clinical and experimental pathology2015

The expression of marker for endometrial stem cell and fibrosis was increased in intrauterine adhesious.

Jianguo Hu, Biao Zeng, Xingwei Jiang, Lina Hu, Ying Meng, Yi Zhu, Min Mao

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

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  15. Tiaoshen Tongluo Attenuates Fibrosis by Modulating the TGF-Evidence-based complementary and alternative medicine : eCAM · 2021
    Article
  16. Article
  17. An update on stem cell therapy for Asherman syndrome.Journal of assisted reproduction and genetics · 2020
    Review
  18. Article
  19. Article
  20. The role of KDR in intrauterine adhesions may involve the TGF-β1/Smads signaling pathway.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    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

7 authors at 1 institution in 1 country.

Jianguo HuDepartment of Obstetrics and Gynecology, Second Affiliated Hospital, Chongqing Medical University Chongqing 400010, China.
Biao ZengDepartment of Obstetrics and Gynecology, Second Affiliated Hospital, Chongqing Medical University Chongqing 400010, China.
Xingwei JiangDepartment of Obstetrics and Gynecology, Second Affiliated Hospital, Chongqing Medical University Chongqing 400010, China.
Lina HuDepartment of Obstetrics and Gynecology, Second Affiliated Hospital, Chongqing Medical University Chongqing 400010, China.
Ying MengDepartment of Obstetrics and Gynecology, Second Affiliated Hospital, Chongqing Medical University Chongqing 400010, China.
Yi ZhuDepartment of Obstetrics and Gynecology, Second Affiliated Hospital, Chongqing Medical University Chongqing 400010, China.
Min MaoDepartment of Obstetrics and Gynecology, Second Affiliated Hospital, Chongqing Medical University Chongqing 400010, China.
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objective of the present study was to evaluate whether fibrotic markers and endometrial stem cell markers were abnormal expressed in endometrium of intrauterine adhesions and a female mouse model for intrauterine adhesions.

methodsWe revaluated endometrial fibrosis using Masson's stain. We detected the expression of endometrium stem cell markers (CD146 and CD140b) and fibrosis markers (TGF-Beta, CTGF, collagen protein I and collagen protein III) in endometrial tissue with intrauterine adhesions using real-time PCR and S-P (Streptavidin-Peroxidase) immunohistochemistry. We create a female mouse model for intrauterine adhesions using mechanical injury, and then revalue the expression of endometrial stem cell markers and fibrosis markers in endometrial tissue of mouse model for intrauterine adhesions.

resultsThe ratio of the area with endometrial fibrosis to total endometrial area in intrauterine adhesious significantly increased compared with the normal endometrial tissue (P < 0.05); The expression levels of fibrotic markers and endometrial stem cell markers were higher in the endometrial tissue with intrauterine adhesious compared to normal endometrial tissue (P < 0.05). The animal experiments showed that the ratio of the area with endometrial fibrosis to total endometrial area significantly increased compared with the control group (P < 0.05); The expression levels of fibrotic markers and endometrial stem cell markers were higher in the endometrial tissue compared to the control group (P < 0.05).

conclusionAberrant activation of fibrosis may be involved in the pathology of intrauterine adhesious.

Indexed as

AdultAnimalsBiomarkersBlotting, WesternDisease Models, AnimalEndometriumFemaleFibrosisHumansImmunohistochemistryMiceMiddle AgedReal-Time Polymerase Chain ReactionStem CellsUterine DiseasesUterusBiomarkersfibrosisintrauterine adhesiousStem cells

Identifiers

PMID25973037
PMCPMC4396235
OpenAlexW2410323842

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.