Evidence map›Paper›PMID 19229297›Full record

ArticleThe EMBO journal2009

Transcription and signalling pathways involved in BCR-ABL-mediated misregulation of 24p3 and 24p3R.

Zhi Sheng, Shu-Zong Wang, Michael R Green

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  3. NOXA expression drives synthetic lethality to RUNX1 inhibition in pancreatic cancer.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  14. Transcription factor ATF5 is required for terminal differentiation and survival of olfactory sensory neurons.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  15. Article
  16. Article
  17. Article
  18. The v-myc-induced Q83 lipocalin is a siderocalin.The Journal of biological chemistry · 2010
    Article
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Zhi ShengHoward Hughes Medical Institute, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Shu-Zong Wang
Michael R Green
University of Massachusetts Chan Medical School · USHoward Hughes Medical Institute · US

Funding

Role of Lipocalin 24p3 in Apoptosis and LeukemiaR01CA115817 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GREEN, MICHAEL R · 2006 to 2010
$1.3M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA115817
6 · The paper itself

Abstract

Lipocalin 24p3 is a secreted protein that can induce apoptosis in cells containing the 24p3 cell surface receptor, 24p3R. The oncoprotein BCR-ABL activates 24p3 and represses 24p3R expression. Thus, BCR-ABL(+) cells synthesise and secrete 24p3, which induces apoptosis in normal 24p3R-containing cells but not in BCR-ABL(+) cells. The cell signalling and transcription factor pathways by which BCR-ABL misregulates expression of 24p3 and 24p3R remain to be elucidated. Here we show that BCR-ABL upregulates 24p3 expression through activation of the JAK/STAT pathway, which culminates in binding of Stat5 to the 24p3 promoter. We find that 24p3R expression is regulated by Runx transcription factors, and that BCR-ABL induces a switch in binding from Runx3, an activator of 24p3R expression, to Runx1, a repressor of 24p3R expression, through a Ras signalling pathway. Finally, we show that repression of 24p3R by BCR-ABL is a critical feature of the mechanism by which imatinib kills BCR-ABL(+) cells. Our results reveal diverse signalling/transcription pathways that regulate 24p3 and 24p3R expression in response to BCR-ABL and are directly relevant to the treatment of BCR-ABL(+) disease.

Indexed as

Signal TransductionTranscription, GeneticAnimalsBenzamidesCore Binding Factor Alpha 2 SubunitDown-RegulationFemaleFusion Proteins, bcr-ablHumansImatinib MesylateLipocalinsMaleMiceMice, Inbred StrainsMice, SCIDPiperazinesBenzamidesCore Binding Factor Alpha 2 SubunitFusion Proteins, bcr-ablImatinib MesylateLipocalinsPiperazinesProto-Oncogene Proteins p21(ras)PyrimidinesReceptors, Cell Surface

Identifiers

PMID19229297
PMCPMC2670863
OpenAlexW2129684490

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.