Evidence map›Paper›PMID 17156427›Full record

ArticleBMC cell biology2006

Differential growth factor regulation of aspartyl-(asparaginyl)-beta-hydroxylase family genes in SH-Sy5y human neuroblastoma cells.

Stephanie A Lahousse, Jade J Carter, Xaolai J Xu, Jack R Wands, Suzanne M de la Monte

Open access · goldAbstract read
In one paragraph

Article in BMC cell biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

36 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Aspartate β-hydroxylase as a target for cancer therapy.Journal of experimental & clinical cancer research : CR · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Ferroportin deficiency impairs manganese metabolism in flatiron mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  18. Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Stephanie A LahousseDepartments of Medicine and Pathology, Rhode Island Hospital, Brown Medical School, and the Pathobiology Graduate Program, Brown University, Providence, RI, USA. Lahousses@niehs.nih.gov <Lahousses@niehs.nih.gov>
Jade J Carter
Xaolai J Xu
Jack R Wands
Suzanne M de la Monte
Brown University · USRhode Island Hospital · US

Funding

FASD Inhibition of ASPH-Notch Mediates Adolescent Cerebral White Matter Pathology-Potential Utility of Non-invasive Extracellular Vesicle AssaysR01AA011431 · NIAAA · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI SUZANNE M. DE LA MONTE · 1996 to 2026
$5.4M
Ethanol, IRS-1 Signaling and Neuronal MigrationR37AA011431 · NIAAA · RHODE ISLAND HOSPITAL · PI DE LA MONTE, SUZANNE M. · 2009 to 2018
$3.7M
EFFECTS OF ETHANOL ON INSULIN SIGNALING IN THE BRAINR01AA012908 · NIAAA · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI DE LA MONTE, SUZANNE M. · 2003 to 2013
$3.0M
PATHOGENESIS, IMMUNODIAGNOSIS AND THERAPY OF HCCR37CA035711 · NCI · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI WANDS, JACK R · 2000 to 2008
$2.9M
EFFECTS OF ALCOHOL ON THE LIVERR01AA002666 · NIAAA · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI WANDS, JACK R · 1985 to 2007
$2.6M
Research Training Program in GastroenterologyT32DK060415 · NIDDK · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI WANDS, JACK R · 2003 to 2013
$1.5M
ETHANOL, INSULIN/IGF SIGNALING AND NEURONAL MIGRATIONR56AA011431 · NIAAA · RHODE ISLAND HOSPITAL · PI DE LA MONTE, SUZANNE M. · 2008 to 2008
$312k
EFFECTS OF ALCOHOL ON THE LIVERR37AA002666 · NIAAA · MASSACHUSETTS GENERAL HOSPITAL · PI WANDS, JACK R · 1989 to 1997
–
PATHOGENESIS, IMMUNODIAGNOSIS, AND THERAPY OF HCCR01CA035711 · NCI · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI WANDS, JACK R · 1985 to 1999
–
NCI NIH HHS CA-35711NCI NIH HHS R01 CA035711NCI NIH HHS R37 CA035711NIAAA NIH HHS AA-02169NIAAA NIH HHS AA-02666NIAAA NIH HHS AA-11431NIAAA NIH HHS AA-12908NIAAA NIH HHS R01 AA002666NIAAA NIH HHS R01 AA011431NIAAA NIH HHS R01 AA012908NIAAA NIH HHS R37 AA002666NIAAA NIH HHS R37 AA011431NIAAA NIH HHS R56 AA011431NIDDK NIH HHS T32 DK060415NIDDK NIH HHS T32 DK60415
6 · The paper itself

Abstract

backgroundAspartyl (asparaginyl)-beta-hydroxylase (AAH) hydroxylates Asp and Asn residues within EGF-like domains of Notch and Jagged, which mediate cell motility and differentiation. This study examines the expression, regulation and function of AAH, and its related transcripts, Humbug and Junctin, which lack catalytic domains, using SH-Sy5y neuroblastoma cells.

resultsReal time quantitative RT-PCR demonstrated 8- or 9-fold higher levels of Humbug than AAH and Junctin, and lower levels of all 3 transcripts in normal human brains compared with neuroblastic tumor cells. AAH and Humbug expression were significantly increased in response to insulin and IGF-I stimulation, and these effects were associated with increased directional motility. However, over-expression of AAH and not Humbug significantly increased motility. Treatment with chemical inhibitors of Akt, Erk MAPK, or cyclin-dependent kinase 5 (Cdk-5) significantly reduced IGF-I stimulated AAH and Humbug expression and motility relative to vehicle-treated control cells. In addition, significantly increased AAH and Humbug expression and directional motility were observed in cells co-transfected with Cdk-5 plus its p35 or p25 regulatory partner. Further studies demonstrated that activated Cdk-5 mediated its stimulatory effects on AAH through Erk MAPK and PI3 kinase.

conclusionAAH and Humbug are over-expressed in SH-Sy5y neuroblastoma cells, and their mRNAs are regulated by insulin/IGF-1 signaling through Erk MAPK, PI3 kinase-Akt, and Cdk-5, which are known mediators of cell migration. Although AAH and Humbug share regulatory signaling pathways, AAH and not Humbug mediates directional motility in SH-Sy5y neuroblastoma cells.

Indexed as

Gene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticBrainCalcium-Binding ProteinsCell Line, TumorCell MovementDNA-Binding ProteinsExtracellular Signal-Regulated MAP KinasesGene Expression RegulationHumansHypoglycemic AgentsInsulinInsulin-Like Growth Factor IMembrane ProteinsMixed Function OxygenasesMuscle Proteinsaspartic acid 2-oxoglutarate-dependent dioxygenaseASPH protein, humanCalcium-Binding ProteinsDNA-Binding ProteinsExtracellular Signal-Regulated MAP KinasesHypoglycemic AgentsIGHMBP2 protein, humanInsulinInsulin-Like Growth Factor IMembrane ProteinsMixed Function OxygenasesMuscle ProteinsNerve Tissue Proteinsneuronal Cdk5 activator (p25-p35)Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTranscription Factors

Identifiers

PMID17156427
PMCPMC1764734
OpenAlexW2110685311

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.