Evidence map›Paper›PMID 10793082›Full record

ArticleThe American journal of pathology2000

Expression of the ALK tyrosine kinase gene in neuroblastoma.

L Lamant, K Pulford, D Bischof, S W Morris, D Y Mason, G Delsol, B Mariamé

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

81 citing papers in PubMed, 229 citations in OpenAlex.

  1. Review
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  3. Article
  4. Comparison ofHeliyon · 2024
    Article
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  16. Article
  17. Review
  18. Targets and Antibody Formats for Immunotherapy of Neuroblastoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
    Review
  19. Review
  20. Observational

21 more citing papers are in PubMed but not listed here.

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 3 countries.

L LamantDepartment of Pathology, Centre Hospitalo-Universitaire Purpan, Toulouse, France.
K Pulford
D Bischof
S W Morris
D Y Mason
G Delsol
B Mariamé
John Radcliffe Hospital · GBCentre National de la Recherche Scientifique · FRSt. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
NPM-ALK AND ALK IN LYMPHOMA AND NORMAL DEVELOPMENTR01CA069129 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MORRIS, STEPHAN W · 1996 to 2006
$2.0M
NCI NIH HHS CA 21765NCI NIH HHS CA 69129NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA069129
6 · The paper itself

Abstract

ALK (anaplastic lymphoma kinase) is a tyrosine kinase receptor, expressed as part of the chimeric NPM-ALK protein, in anaplastic large cell lymphomas (ALCLs) exhibiting the t(2;5)(p23;q35) translocation. As a result of this translocation, the NPM (nucleophosmin) gene is fused to the portion of the ALK gene encoding its intracytoplasmic segment. In normal mouse tissues, mRNA encoding the Alk receptor has been found only in neural cells, suggesting involvement of this receptor in the development of the nervous system. The purpose of the present study was to examine the presence of ALK transcripts and protein in normal human tissues and a variety of cell lines and human tumors. Emphasis was placed on neuroblastomas because other tyrosine kinase receptors are expressed in human neuroblastomas. Fifty-six cell lines, including 29 lines of neural origin, and lymphoid and nonlymphoid tissue specimens, including 24 neuroblastomas, were investigated for ALK expression, using reverse transcriptase-polymerase chain reaction, Western blotting, and immunohistochemistry. The results confirmed that mRNA encoding ALK protein was not detectable in any normal or neoplastic hematopoietic tissue tested, except for t(2;5)-positive ALCL. The salient finding was that 13 of the 29 cell lines of neural origin and 22 of 24 neuroblastomas were found to express ALK transcripts and ALK protein. However, no correlation was evident between any known prognostic factors and the level of ALK expression.

Indexed as

Anaplastic Lymphoma KinaseBlotting, WesternChildChild, PreschoolGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHumansImmunohistochemistryInfantInfant, NewbornNeuroblastomaPrecipitin TestsProtein-Tyrosine KinasesReceptor Protein-Tyrosine KinasesReverse Transcriptase Polymerase Chain ReactionRNA, MessengerALK protein, humanAlk protein, mouseAnaplastic Lymphoma KinaseProtein-Tyrosine KinasesReceptor Protein-Tyrosine KinasesRNA, Messenger

Identifiers

PMID10793082
PMCPMC1876934
OpenAlexW1975686452

What OpenQuestion holds

Textmetadata
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.