Evidence map›Paper›PMID 24551273›Full record

ArticleInternational journal of clinical and experimental pathology2014

Expression analysis of BMP2, BMP5, BMP10 in human colon tissues from Hirschsprung disease patients.

Mei Wu, Wenwen Chen, Jie Mi, Dong Chen, Weilin Wang, Hong Gao

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. BMP signaling pathway member expression is enriched in enteric neural progenitors and required for zebrafish enteric nervous system development.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Article
  2. Expression of bone morphogenetic protein 10 in cases with endometrial carcinoma and its clinical significance.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Article
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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.

Mei WuKey Laboratory of Health Ministry for Congenital Malformations, Shengjing Hospital of China Medical University Shenyang, Liaoning, People's Republic of China.
Wenwen ChenImaging and Nuclear Medicine, Shengjing Hospital of China Medical University 36 Sanhao Street, Shenyang, Liaoning, 110004, The People's Republic of China.
Jie MiKey Laboratory of Health Ministry for Congenital Malformations, Shengjing Hospital of China Medical University Shenyang, Liaoning, People's Republic of China.
Dong ChenKey Laboratory of Health Ministry for Congenital Malformations, Shengjing Hospital of China Medical University Shenyang, Liaoning, People's Republic of China.
Weilin WangPediatric Surgery, Shengjing Hospital of China Medical University 36 Sanhao Street, Shenyang, Liaoning, 110004, The People's Republic of China.
Hong GaoKey Laboratory of Health Ministry for Congenital Malformations, Shengjing Hospital of China Medical University Shenyang, Liaoning, People's Republic of China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveBone morphogenetic proteins (BMPs) are members of the transforming growth factor β (TGF β) superfamily. BMP2, BMP5 and BMP10 exert their biological functions by interacting with membrane bound receptors belonging to the serine/threonine kinase family. Hirschsprung disease (HSCR) is characterized by the absence of intramural ganglion cells in the nerve plexuses of the distal gut. However, putative Notch function in enteric nervous system (ENS) development and the etiology of HSCR is unknown.

methodsAganglionic and ganglionic colon segment tissues of 50 HSCR patients were investigated for the expression pattern of BMP2, BMP5 and BMP10 using real-time RT-PCR, Western blot analysis and immunohistochemical staining.

resultsThe mRNA levels of BMP2, BMP5 and BMP10 in the stenotic colon segment from HSCR patients were significantly higher than those in the normal ones. Similar increased expressions of them in the stenotic colon segments were detected by Western blotting coupled with densitometry analysis. Lastly, immunohistologicl stain showed significant BMP2, 5 and 10 increases in mucous and muscular layers from stenotic colon segments compared to normal segments.

conclusionsBMP2, BMP5 and BMP10 are elevated in the stenotic colon segment of HSCR, and BMPs signaling plays a pivotal role in the development of HSCR.

Indexed as

Blotting, WesternBone Morphogenetic Protein 2Bone Morphogenetic Protein 5Bone Morphogenetic ProteinsChild, PreschoolColonFemaleHirschsprung DiseaseHumansImmunohistochemistryInfantIntestinal MucosaMaleReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionRNA, MessengerBMP10 protein, humanBMP2 protein, humanBMP5 protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 5Bone Morphogenetic ProteinsRNA, MessengerBone morphogenetic proteins (BMPs)enteric nervous system (ENS)ganglion cellHirschsprung disease (HSCR)stenotic colon

Identifiers

PMID24551273
PMCPMC3925897
OpenAlexW67503039

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.