Evidence map›Paper›PMID 21625996›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2011

Anaplastic lymphoma kinase (ALK) inhibitor response in neuroblastoma is highly correlated with ALK mutation status, ALK mRNA and protein levels.

Floor A M Duijkers, José Gaal, Jules P P Meijerink, Pieter Admiraal, Rob Pieters, Ronald R de Krijger, Max M van Noesel

Open access · hybridAbstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Neuroblastoma, a Paradigm for Big Data Science in Pediatric Oncology.International journal of molecular sciences · 2016
    Review
  10. Article
  11. Article
  12. Anaplastic Lymphoma Kinase as a Cancer Target in Pediatric Malignancies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Review
  13. Article
  14. Article
  15. Review
  16. 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 2 institutions in 1 country.

Floor A M DuijkersDepartment of Pediatric Oncology-Hematology, Erasmus MC- Sophia Children's Hospital, Dr. Molewaterplein 60, 3015 GJ, Rotterdam, The Netherlands. f.duijkers@erasmusmc.nl
José Gaal
Jules P P Meijerink
Pieter Admiraal
Rob Pieters
Ronald R de Krijger
Max M van Noesel
Erasmus MC - Sophia Children’s Hospital · NLErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn pediatric neuroblastoma (NBL), high anaplastic lymphoma kinase (ALK) levels appear to be correlated with an unfavorable prognosis, regardless of ALK mutation status. This suggests a therapeutic role for ALK inhibitors in NBL patients. We examined the correlation between levels of ALK, phosphorylated ALK (pALK) and downstream signaling proteins and response to ALK inhibition in a large panel of both ALK mutated and wild type (WT) NBL cell lines.

methodsWe measured protein levels by western blot and ALK inhibitor sensitivity (TAE684) by viability assays in 19 NBL cell lines of which 6 had a point mutation and 4 an amplification of the ALK gene.

resultsALK 220 kDa (p = 0.01) and ALK 140 kDa (p = 0.03) protein levels were higher in ALK mutant than WT cell lines. Response to ALK inhibition was significantly correlated with ALK protein levels (p < 0.01). ALK mutant cell lines (n = 4) were 14,9 fold (p < 0,01) more sensitive to ALK inhibition than eight WT cell lines.

conclusionNBL cell lines often express ALK at high levels and are responsive to ALK inhibitors. Mutated cell lines express ALK at higher levels, which may define their superior response to ALK inhibition.

Indexed as

Gene Expression Regulation, NeoplasticAnaplastic Lymphoma KinaseCell DifferentiationCell Line, TumorCell SurvivalExtracellular Signal-Regulated MAP KinasesGene DosageHumansMutationNeuroblastomaNeuronsPhosphorylationProtein Kinase InhibitorsPyrimidinesReceptor Protein-Tyrosine KinasesRNA, MessengerALK protein, humanAnaplastic Lymphoma KinaseExtracellular Signal-Regulated MAP KinasesNVP-TAE684Protein Kinase InhibitorsPyrimidinesReceptor Protein-Tyrosine KinasesRNA, Messenger

Identifiers

PMID21625996
PMCPMC3219872
OpenAlexW1991590017

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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.