Evidence map›Paper›PMID 29118923›Full record

ArticleAmerican journal of translational research2017

DDX3 binding with CK1ε was closely related to motor neuron degeneration of ALS by affecting neurite outgrowth.

Yanchun Chen, Qing Wang, Qiaozhen Wang, Huancai Liu, Fenghua Zhou, Yawen Zhang, Meng Yuan, Chunyan Zhao, Yingjun Guan, Xin Wang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

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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

10 authors at 1 institution in 2 countries.

Yanchun ChenDepartment of Histology and Embryology, Weifang Medical UniversityWeifang, Shandong, PR China.
Qing WangDepartment of Human Anatomy, Weifang Medical UniversityWeifang, Shandong, PR China.
Qiaozhen WangDepartment of Human Anatomy, Weifang Medical UniversityWeifang, Shandong, PR China.
Huancai LiuDepartment of Joint Surgery, Affiliated Hospital, Weifang Medical UniversityWeifang, Shandong, PR China.
Fenghua ZhouDepartment of Pathology, Weifang Medical UniversityWeifang, Shandong, PR China.
Yawen ZhangDepartment of Histology and Embryology, Weifang Medical UniversityWeifang, Shandong, PR China.
Meng YuanDepartment of Histology and Embryology, Weifang Medical UniversityWeifang, Shandong, PR China.
Chunyan ZhaoDepartment of Histology and Embryology, Weifang Medical UniversityWeifang, Shandong, PR China.
Yingjun GuanDepartment of Histology and Embryology, Weifang Medical UniversityWeifang, Shandong, PR China.
Xin WangDepartment of Histology and Embryology, Weifang Medical UniversityWeifang, Shandong, PR China.
Weifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a chronic neurodegenerative disease characterized by progressive degeneration of motor neurons. The pathogenesis of ALS remains largely unknown. RNA helicase DDX3 is a multifunctional protein involved in several steps of gene expression. Casein kinase 1ε (CK1ε) is an important signal molecule of Wnt signaling pathway and is closely related to neurite growth. However, the roles of DDX3 and CK1ε in the pathogenesis of ALS remain unclear. In this study, we first investigated the expression of DDX3 and CK1ε in the spinal cord of SOD1-G93A ALS transgenic mice using RT-PCR, Western blot and immunohistochemical technique. Results showed that the altered expression of DDX3 and CK1ε was found in the spinal cord of ALS mice. DDX3 and CK1ε positive cells were mainly distributed in the anterior horn of spinal cord and co-localized with neurons not with glial cells, suggesting that the altered expression of DDX3 and CK1ε was closely related to motor neuron degeneration of ALS. Moreover, we selected NSC34 cell line and transfected pEGFP-G93A-SOD1 plasmid to further examine the mechanism. Knockdown of DDX3 that uses small interfering RNA (siRNA) decreased the mRNA and protein levels of CK1ε significantly and inhibited neurite outgrowth of SOD1 mutant NSC34 cells in vitro. Co-immunoprecipitation kit confirmed that DDX3 could band with CK1ε in vivo. Our data suggested that DDX3 binding with CK1ε was closely related to motor neuron degeneration of ALS by affecting neurite outgrowth. Thus, elucidating the underlying mechanisms of ALS is crucial for future development of ALS treatments.

Indexed as

Amyotrophic lateral sclerosisCK1εDDX3NSC34 cellsSOD1-G93A transgenic mice

Identifiers

PMID29118923
PMCPMC5666070
OpenAlexW2947152919

What OpenQuestion holds

Textmetadata
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Registered trials

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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.