Evidence map›Paper›PMID 11960373›Full record

ArticleOncogene2002

Induction of the interleukin-2/15 receptor beta-chain by the EWS-WT1 translocation product.

Jenise C Wong, Sean B Lee, Moshe D Bell, Paul A Reynolds, Emilio Fiore, Ivan Stamenkovic, Vivi Truong, Jonathan D Oliner, William L Gerald, Daniel A Haber

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. 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
3.9field-weighted citation impact, top 7% 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, 47 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Soft tissue tumors associated with EWSR1 translocation.Virchows Archiv : an international journal of pathology · 2010
    Review
  13. Article
  14. Article
  15. Article
  16. 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

10 authors at 4 institutions in 1 country.

Jenise C WongMassachusetts General Hospital Cancer Center and Harvard Medical School, Charlestown, Massachusetts, MA 02129, USA.
Sean B Lee
Moshe D Bell
Paul A Reynolds
Emilio Fiore
Ivan Stamenkovic
Vivi Truong
Jonathan D Oliner
William L Gerald
Daniel A Haber
Massachusetts General Hospital · USMemorial Sloan Kettering Cancer Center · USAmgen (United States) · USHarvard University · US

Funding

Functional Properties of the Wilms' Tumor Gene WT1R37CA058596 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HABER, DANIEL A. · 2003 to 2011
$3.9M
MUTATIONAL AND FUNCTIONAL ANALYSIS OF WILMS'TUMORR01CA058596 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HABER, DANIEL A. · 1993 to 2002
$965k
EWS-WT1 GENE FUSION IN DESMOPLASTIC SMALL CELL TUMORR01CA068273 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI GERALD, WILLIAM L · 1996 to 1998
–
NCI NIH HHS CA58596NCI NIH HHS CA68273
6 · The paper itself

Abstract

EWS-WT1 is a chimeric transcription factor resulting from fusion of the N-terminal domain of the Ewing sarcoma gene EWS to the three C-terminal zinc fingers of the Wilms tumor suppressor WT1. This translocation underlies desmoplastic small round cell tumor (DSRCT), which is noted for the abundance of reactive stroma surrounding islets of tumor cells, suggestive of paracrine signals contributing to tumor cell proliferation. Hybridization to high-density oligonucleotide microarrays can be used to identify targets of EWS-WT1. Expression of EWS-WT1 from a tetracycline-regulated promoter leads to the induction of growth-associated genes, of which the most remarkable is the beta-chain of the interleukin-2/15 receptor (IL-2/15Rbeta). Potent transcriptional activation by the chimeric protein maps to two bindings sites within the IL-2/15Rbeta promoter. Analysis of primary DSRCT tumor specimens demonstrates high levels of IL-2/15Rbeta within the tumor cells, along with expression of IL-2 and IL-15 by the abundant hyperplastic endothelial cells within the reactive stroma. Activation of this cytokine signaling pathway is consistent with the nuclear localization of its downstream effectors, phosphorylated STAT3 and STAT5. These observations suggest that the transcriptional induction of a cytokine receptor by a tumor-associated translocation product enables a proliferative response of epithelial cancer cells to ligands secreted by the surrounding stroma.

Indexed as

Gene Expression Regulation, NeoplasticMilk ProteinsAbdominal NeoplasmsCarcinoma, Small CellDNA-Binding ProteinsElectrophoretic Mobility Shift AssayHumansImmunohistochemistryInterleukin-2Interleukin-2 Receptor beta SubunitInterleukin-5Janus Kinase 1Janus Kinase 3MaleOligonucleotide Array Sequence AnalysisOncogene Proteins, FusionDNA-Binding ProteinsEWS1-WT1 fusion protein, humanIL15RA protein, humanIL2RB protein, humanInterleukin-2Interleukin-2 Receptor beta SubunitInterleukin-5JAK1 protein, humanJAK3 protein, humanJanus Kinase 1Janus Kinase 3Milk ProteinsOncogene Proteins, FusionProtein-Tyrosine KinasesReceptors, InterleukinReceptors, Interleukin-15Receptors, Interleukin-2RNA, MessengerSTAT3 protein, humanSTAT3 Transcription FactorSTAT5 Transcription FactorTrans-Activators

Identifiers

PMID11960373
OpenAlexW1978335750

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.