Evidence map›Paper›PMID 17360941›Full record

ArticleBlood2007

A novel fusion of RBM6 to CSF1R in acute megakaryoblastic leukemia.

Ting-lei Gu, Thomas Mercher, Jeffrey W Tyner, Valerie L Goss, Denise K Walters, Melanie G Cornejo, Cynthia Reeves, Lana Popova, Kimberly Lee, Michael C Heinrich and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  8. Article
  9. Review
  10. RNA-Binding Proteins in Acute Leukemias.International journal of molecular sciences · 2020
    Review
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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

16 authors at 5 institutions in 2 countries.

Ting-lei GuCell Signaling Technology, Danvers, MA 01923, USA.
Thomas Mercher
Jeffrey W Tyner
Valerie L Goss
Denise K Walters
Melanie G Cornejo
Cynthia Reeves
Lana Popova
Kimberly Lee
Michael C Heinrich
John Rush
Masanori Daibata
Isao Miyoshi
D Gary Gilliland
Brian J Druker
Roberto D Polakiewicz
Cell Signaling Technology (United States) · USHoward Hughes Medical Institute · USBrigham and Women's Hospital · USKōchi University · JPOregon Health & Science University · US

Funding

TYROSINE KINASE ONCOGENESIS IN MYELOID LEUKEMIAP01CA066996 · NCI · DANA-FARBER CANCER INSTITUTE · PI SCOTT A ARMSTRONG · 1996 to 2026
$52.5M
NCI NIH HHS P01 CA066996NCI NIH HHS R01 CA66996
6 · The paper itself

Abstract

Activated tyrosine kinases have been frequently implicated in the pathogenesis of cancer, including acute myeloid leukemia (AML), and are validated targets for therapeutic intervention with small-molecule kinase inhibitors. To identify novel activated tyrosine kinases in AML, we used a discovery platform consisting of immunoaffinity profiling coupled to mass spectrometry that identifies large numbers of tyrosine-phosphorylated proteins, including active kinases. This method revealed the presence of an activated colony-stimulating factor 1 receptor (CSF1R) kinase in the acute megakaryoblastic leukemia (AMKL) cell line MKPL-1. Further studies using siRNA and a small-molecule inhibitor showed that CSF1R is essential for the growth and survival of MKPL-1 cells. DNA sequence analysis of cDNA generated by 5'RACE from CSF1R coding sequences identified a novel fusion of the RNA binding motif 6 (RBM6) gene to CSF1R gene generated presumably by a t(3;5)(p21;q33) translocation. Expression of the RBM6-CSF1R fusion protein conferred interleukin-3 (IL-3)-independent growth in BaF3 cells, and induces a myeloid proliferative disease (MPD) with features of megakaryoblastic leukemia in a murine transplant model. These findings identify a novel potential therapeutic target in leukemogenesis, and demonstrate the utility of phosphoproteomic strategies for discovery of tyrosine kinase alleles.

Indexed as

AnimalsCell LineCell Line, TumorCell ProliferationCell SurvivalChromosomes, Human, Pair 3Chromosomes, Human, Pair 5HumansLeukemia, Megakaryoblastic, AcuteMiceNeoplasm TransplantationOncogene Proteins, FusionProtein-Tyrosine KinasesReceptor, Macrophage Colony-Stimulating FactorRNA-Binding ProteinsSequence Analysis, DNAOncogene Proteins, FusionProtein-Tyrosine KinasesRBM6 protein, humanReceptor, Macrophage Colony-Stimulating FactorRNA-Binding Proteins

Identifiers

PMID17360941
PMCPMC1896120
OpenAlexW2079564298

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.