Evidence map›Paper›PMID 34455465›Full record

ArticlePediatric surgery international2022

KDM5B promotes cell migration by regulating the noncanonical Wnt/PCP pathway in Hirschsprung's disease.

Ting Yao, Zhilin Xu, Zenghui Hao, You Yu, Bingxue Liang, Shuyu Wang

Abstract read
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In one paragraph

Article in Pediatric surgery international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 82% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 1 country.

Ting YaoDepartment of Pediatric Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China.
Zhilin XuDepartment of Pediatric Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China.
Zenghui HaoDepartment of Pediatric Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China.
You YuDepartment of Pediatric Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China.
Bingxue LiangDepartment of Pediatric Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China.
Shuyu WangDepartment of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China. shuyuwang_hyd@hotmail.com.ORCID http://orcid.org/0000-0002-4688-066X
Harbin Medical University · CN

Funding

the doctoral fund of the first affiliated hospital of harbin medical university 2020B22
6 · The paper itself

Abstract

purposeWe measured the expression of the histone demethylase lysine-specific demethylase 5B (KDM5B) in the bowels of patients with Hirschsprung's disease (HSCR) and investigated the molecular mechanism by which KDM5B promotes the migration of neuronal PC12 cells.

methodsKDM5B expression was detected in the ganglionic and aganglionic colon of patients with HSCR (n = 10) and controls (n = 10). The expression and localization of KDM5B were assessed using immunohistochemical and immunofluorescence staining. Real-time PCR and Western blotting were performed to quantify KDM5B expression. The migration was determined using Transwell and wound-healing assays. G-LISA, GTPase pulldown and luciferase-based reporter gene assays were performed to evaluate the key components of Wnt/planar cell polarity (PCP) signaling in vitro.

resultsOur current study showed that KDM5B colocalized with neurons. KDM5B expression was reduced in HSCR specimens, while the aganglionic segments showed the greatest reduction. KDM5B knockdown inhibited the migration of PC12 cells. Moreover, inhibition of KDM5B decreased the expression of key genes in the Wnt/PCP pathway, and its inhibitory effect on PC12 cell migration was reversed by Wnt5a treatment.

conclusionsKDM5B promotes neuronal migration via the Wnt/PCP pathway. A potential role for KDM5B in altered enteric nervous system development in HSCR warrants further investigation.

Indexed as

Hirschsprung DiseaseCell MovementColonGangliaHumansIntestinesJumonji Domain-Containing Histone DemethylasesNuclear ProteinsRepressor ProteinsJumonji Domain-Containing Histone DemethylasesKDM5B protein, humanNuclear ProteinsRepressor ProteinsHirschsprung’s diseaseHistone demethylaseKDM5BNeural crest cellsWnt/PCP pathway

Identifiers

PMID34455465
OpenAlexW3196748774

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.