Evidence map›Paper›PMID 19131339›Full record

ArticleThe Journal of biological chemistry2009

Oxidative stress promotes transcriptional up-regulation of Fyn in BCR-ABL1-expressing cells.

Yin Gao, Adrienne Howard, Kechen Ban, Joya Chandra

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Combination of HDAC and FYN inhibitors in synovial sarcoma treatment.Frontiers in cell and developmental biology · 2024
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
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  11. Article
  12. Oxidative stress responses and NRF2 in human leukaemia.Oxidative medicine and cellular longevity · 2015
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Tyrosine phosphorylation controls nuclear export of Fyn, allowing Nrf2 activation of cytoprotective gene expression.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    Article
  19. 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

4 authors at 1 institution in 1 country.

Yin GaoDepartment of Pediatrics Research, Unit 853, Children's Cancer Hospital at M. D. Anderson, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Adrienne Howard
Kechen Ban
Joya Chandra
The University of Texas MD Anderson Cancer Center · US

Funding

Role of Redox Dependent Signaling in LeukemiaR01CA115811 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CHANDRA, JOYA · 2007 to 2010
$1.3M
NCI NIH HHS R01 CA 115811
6 · The paper itself

Abstract

Signaling initiated by the BCR-ABL1 kinase causes chronic myelogenous leukemia (CML). Recently, we reported that expression of Fyn, a Src kinase, is heightened in CML cells and patient specimens and confers in vitro and in vivo proliferative advantages. Fyn is regulated by redox, and because BCR-ABL1 raises intracellular oxidant levels, which have been implicated in CML progression, we explored the molecular regulation of Fyn. Here we identify the transcription factors that drive redox- and BCR-ABL1-dependent Fyn expression. Promoter deletion analysis in 293T, BaF3, BaF3-p210, and K562 cells identified the region essential for basal transcriptional activity. Mutation of Sp1 and Egr1 binding sites within the essential region diminished Fyn promoter activity and identified Egr1 as conferring redox sensitivity. Gel shift and chromatin immunoprecipitation assays confirmed the binding of Sp1 and Egr1 to the promoter fragments. Importantly, knockdown of Sp1 or Egr1 with small interference RNA or inhibition of Sp1 binding by mithramycin A repressed Fyn protein expression. Our work is the first to define transcription factors that are responsible for endogenous, oxidative stress-dependent and BCR-ABL1-dependent Fyn expression.

Indexed as

Early Growth Response Protein 1Fusion Proteins, bcr-ablHumansK562 CellsOxidation-ReductionOxidative StressProto-Oncogene Proteins c-fynResponse ElementsRNA, Small InterferingSp1 Transcription FactorTranscription, GeneticUp-RegulationEarly Growth Response Protein 1EGR1 protein, humanFusion Proteins, bcr-ablFYN protein, humanProto-Oncogene Proteins c-fynRNA, Small InterferingSp1 Transcription Factor

Identifiers

PMID19131339
PMCPMC2652262
OpenAlexW2078518903

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.