Evidence map›Paper›PMID 26973341›Full record

ArticleBMB reports2016

Critical role of protein L-isoaspartyl methyltransferase in basic fibroblast growth factor-mediated neuronal cell differentiation.

To Thi Mai Dung, Young-Su Yi, Jieun Heo, Woo Seok Yang, Ji Hye Kim, Han Gyung Kim, Jae Gwang Park, Byong Chul Yoo, Jae Youl Cho, Sungyoul Hong

Open access · goldAbstract readNews
In one paragraph

Article in BMB reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Protein Kinase C Theta Modulates PCMT1 through hnRNPL to Regulate FOXP3 Stability in Regulatory T Cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  3. Article
  4. 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

10 authors at 2 institutions in 1 country.

To Thi Mai DungDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Young-Su YiDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419; Department of Pharmaceutical Engineering, Cheongju University, Cheongju 28503, Korea.
Jieun HeoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Woo Seok YangDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Ji Hye KimDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Han Gyung KimDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Jae Gwang ParkDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Byong Chul YooColorectal Cancer Branch, Research Institute, National Cancer Center, Goyang 10408, Korea.
Jae Youl ChoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Sungyoul HongDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea.
Sungkyunkwan University · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to study the role of protein L-isoaspartyl methyltransferase (PIMT) in neuronal differentiation using basic fibroblast growth factor (bFGF)-induced neuronal differentiation, characterized by cell-body shrinkage, long neurite outgrowth, and expression of neuronal differentiation markers light and medium neurofilaments (NF). The bFGF-mediated neuronal differentiation of PC12 cells was induced through activation of mitogen-activated protein kinase (MAPK) signaling molecules [MAPK kinase 1/2 (MEK1/2), extracellular signal-regulated kinase 1/2 (ERK1/2), and p90RSK], and phosphatidylinositide 3-kinase (PI3K)/Akt signaling molecules PI3Kp110β, PI3Kp110γ, Akt, and mTOR. Inhibitors (adenosine dialdehyde and S-adenosylhomocysteine) of protein methylation suppressed bFGF-mediated neuronal differentiation of PC12 cells. PIMTeficiency caused by PIMT-specific siRNA inhibited neuronal differentiation of PC12 cells by suppressing phosphorylation of MEK1/2 and ERK1/2 in the MAPK signaling pathway and Akt and mTOR in the PI3K/Akt signaling pathway. Therefore, these results suggested that PIMT was critical for bFGF-mediated neuronal differentiation of PC12 cells and regulated the MAPK and Akt signaling pathways. [BMB Reports 2016; 49(8): 437-442].

Indexed as

AnimalsCell DifferentiationFibroblast Growth Factor 2Mitogen-Activated Protein KinasesNeuronsPC12 CellsPhosphatidylinositol 3-KinasesProtein D-Aspartate-L-Isoaspartate MethyltransferaseProto-Oncogene Proteins c-aktRatsSignal TransductionFibroblast Growth Factor 2Mitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesProtein D-Aspartate-L-Isoaspartate MethyltransferaseProto-Oncogene Proteins c-akt

Identifiers

PMID26973341
PMCPMC5070731
OpenAlexW2418110288

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.