Evidence map›Paper›PMID 12147653›Full record

ArticleJournal of clinical pathology2002

Loss of nuclear expression of the p33(ING1b) inhibitor of growth protein in childhood acute lymphoblastic leukaemia.

G S Nouman, J J Anderson, K M Wood, J Lunec, A G Hall, M M Reid, B Angus

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Ectopic expression of p33Oncology letters · 2015
    Article
  3. A novel tumor suppressor gene in basal cell carcinoma: inhibition of growth factor-2.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  4. Article
  5. Article
  6. The ING family tumor suppressors: from structure to function.Cellular and molecular life sciences : CMLS · 2011
    Review
  7. Article
  8. Inhibitor of growth tumor suppressors in cancer progression.Cellular and molecular life sciences : CMLS · 2010
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
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

7 authors at 3 institutions in 2 countries.

G S NoumanPathology Department, Royal Victoria Infirmary, University of Newcastle, Queens Victoria Road, Newcastle upon Tyne, NE1 4PH, UK.
J J Anderson
K M Wood
J Lunec
A G Hall
M M Reid
B Angus
Royal Victoria Infirmary · GBNewcastle University · GBUniversity of Newcastle Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsp33(ING1b) is a tumour suppressor protein involved in growth control and apoptosis. Suppression of p33(ING1b) expression is associated with the loss of cellular growth control and immortalisation, whereas its overexpression causes cell cycle arrest. Moreover, normal p33(ING1b) expression is essential for optimal function of p53. Acute lymphoblastic leukaemia (ALL) is the most common malignancy of childhood, accounting for one third of all childhood malignancies. A variety of cytogenetic abnormalities have been described but there is no single abnormality common to all cases. Deregulation of the TP53 pathway is a common genetic abnormality in human malignancies. However, TP53 mutations are uncommon in ALL. It is possible that alternative mechanisms of regulation of the TP53 apoptosis pathway, such as modulation of p33(ING1b) expression, may be important in ALL. The aim of this study was to assess the expression of p33(ING1b) in childhood ALL.

methodsOne hundred and forty five patients with childhood ALL were investigated in this immunohistochemical study of the expression of p33(ING1b).

resultsLoss of nuclear expression of p33(ING1b) was seen in 78% of cases. This was associated with increased cytoplasmic expression of the protein. Kaplan Meier survival analysis demonstrated a trend towards a better prognosis for patients with tumours that had lost nuclear p33(ING1b).

conclusionThese results suggest that the loss of nuclear p33(ING1b) expression may be an important molecular event in the pathogenesis of childhood ALL.

Indexed as

AdolescentBiomarkers, TumorCell Cycle ProteinsCell NucleusChildChild, PreschoolCytoplasmDNA-Binding ProteinsFemaleFollow-Up StudiesGenes, Tumor SuppressorHumansInfantInfant, NewbornInhibitor of Growth Protein 1Intracellular Signaling Peptides and ProteinsBiomarkers, TumorCell Cycle ProteinsDNA-Binding ProteinsING1 protein, humanInhibitor of Growth Protein 1Intracellular Signaling Peptides and ProteinsNeoplasm ProteinsNuclear ProteinsProteinsTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID12147653
PMCPMC1769716
OpenAlexW2100636148

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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.