Evidence map›Paper›PMID 19716809›Full record

ArticleBiochemical and biophysical research communications2009

Phosphorylation of ARD1 by IKKbeta contributes to its destabilization and degradation.

Hsu-Ping Kuo, Dung-Fang Lee, Weiya Xia, Chien-Chen Lai, Long-Yuan Li, Mien-Chie Hung

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Conformational plasticity links structural instability of NAA10Computational and structural biotechnology journal · 2024
    Article
  3. NAA10 as a New Prognostic Marker for Cancer Progression.International journal of molecular sciences · 2020
    Review
  4. Article
  5. Review
  6. Article
  7. ARD1/NAA10 acetylation in prostate cancer.Experimental & molecular medicine · 2018
    Review
  8. Review
  9. Article
  10. Article
  11. Arrest-defective-1 protein (ARD1): tumor suppressor or oncoprotein?American journal of translational research · 2010
    Article
  12. TNFalpha induces HIF-1alpha expression through activation of IKKbeta.Biochemical and biophysical research communications · 2009
    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 5 institutions in 2 countries.

Hsu-Ping KuoDepartment of Molecular and Cellular Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Dung-Fang Lee
Weiya Xia
Chien-Chen Lai
Long-Yuan Li
Mien-Chie Hung
The University of Texas Health Science Center at Houston · USChina Medical University · TWChina Medical University Hospital · TWNational Chung Hsing University · TWThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS MD ANDERSON SPORE IN OVARIAN CANCERP50CA083639 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BAST, ROBERT C · 1999 to 2015
$33.0M
UTMDACC SPORE in Breast CancerP50CA116199 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BERRY, DONALD A · 2005 to 2009
$11.9M
Tyrosine Kinase-Dependant and - Independent Pathways of EGFR in Breast Cancer ProP01CA099031 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HUNG, MIEN-CHIE · 2003 to 2014
$11.6M
Tumor Progression of Nuclear EGFR in Breast CancerR01CA109311 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HUNG, MIEN-CHIE · 2004 to 2014
$3.0M
NCI NIH HHS CA16672,NCI NIH HHS P01 CA099031NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA083639NCI NIH HHS P50 CA116199NCI NIH HHS P50 CA83639NCI NIH HHS R01 CA109311
6 · The paper itself

Abstract

IkappaB kinase beta (IKKbeta), a major kinase downstream of various proinflammatory signals, mediates multiple cellular functions through phosphorylation and regulation of its substrates. On the basis of protein sequence analysis, we identified arrest-defective protein 1 (ARD1), a protein involved in apoptosis and cell proliferation processes in many human cancer cells, as a new IKKbeta substrate. We provided evidence showing that ARD1 is indeed a bona fide substrate of IKKbeta. IKKbeta physically associated with ARD1 and phosphorylated it at Ser209. Phosphorylation by IKKbeta destabilized ARD1 and induced its proteasome-mediated degradation. Impaired growth suppression was observed in ARD1 phosphorylation-mimic mutant (S209E)-transfected cells as compared with ARD1 non-phosphorylatable mutant (S209A)-transfected cells. Our findings of molecular interactions between ARD1 and IKKbeta may enable further understanding of the upstream regulation mechanisms of ARD1 and of the diverse functions of IKKbeta.

Indexed as

AcetyltransferasesAmino Acid SequenceAnimalsCell Line, TumorCell ProliferationConserved SequenceEnzyme StabilityHumansI-kappa B KinaseMiceMolecular Sequence DataN-Terminal Acetyltransferase AN-Terminal Acetyltransferase EPhosphorylationProteasome Endopeptidase ComplexAcetyltransferasesI-kappa B KinaseNAA10 protein, humanN-Terminal Acetyltransferase AN-Terminal Acetyltransferase EProteasome Endopeptidase Complex

Identifiers

PMID19716809
PMCPMC2753275
OpenAlexW2074878099

What OpenQuestion holds

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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.