Evidence map›Paper›PMID 19409613›Full record

ArticleLeukemia research2009

Downregulation of JUNB mRNA expression in advanced phase chronic myelogenous leukemia.

Koyu Hoshino, Alfonso Quintás-Cardama, Jerald Radich, Hongyui Dai, Hui Yang, Guillermo Garcia-Manero

Abstract read
In one paragraph

Article in Leukemia research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 25 citations in OpenAlex.

  1. JunB: a paradigm for Jun family in immune response and cancer.Frontiers in cellular and infection microbiology · 2023
    Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Inhibition of Ras-mediated signaling pathways in CML stem cells.Cellular oncology (Dordrecht, Netherlands) · 2015
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Koyu HoshinoDepartment of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX 77230-1402, USA.
Alfonso Quintás-Cardama
Jerald Radich
Hongyui Dai
Hui Yang
Guillermo Garcia-Manero
The University of Texas MD Anderson Cancer Center · USFred Hutch Cancer Center · USRosetta Stone (United States) · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KONOPLEVA, MARINA Y · 2003 to 2023
$43.7M
GENE EXPRESSION PROFILE OF PROGRESSION &RESPONSE IN CMLU01CA085053 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RADICH, JERALD P · 1999 to 2003
$1.6M
Cell Cycle Controlling Genes in Adult Acute LymphomaR21CA100067 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI GARCIA-MANERO, GUILLERMO · 2004 to 2005
$272k
NCI NIH HHS CA-100067NCI NIH HHS CA-85053NCI NIH HHS P50 CA100632NCI NIH HHS R21 CA100067
6 · The paper itself

Abstract

JUNB inactivation in transgenic mice results in a myeloproliferative disorder that closely resembles human chronic myelogenous leukemia (CML). It has been reported that downregulation of JUNB expression is a universal phenomenon in patients with CML due aberrant DNA methylation of its promoter. Based on this, we studied methylation and gene expression levels of JUNB in CML. We analyzed the methylation status of the JUNB gene in 6 cell lines and in 102 patients with CML using several bisulfite PCR assays. JUNB expression was analyzed using real-time PCR and gene expression profiling. JUNB methylation was not observed in any of the cell lines studied, and only in 3% of patients with CML. Despite the lack of JUNB methylation, JUNB was expressed at low levels both in CML cell lines (median dCT -6.86; range -5.87 to -9.61), and in patients with CML in blastic phase (BP) (median dCT -3.95; range -1.48 to -6.29) (p = 0.002). Finally, we evaluated JUNB expression in 82 additional patients with CML by gene expression arrays. We found that JUNB was significantly downregulated in advanced phase CML in contrast to chronic phase CML (median log ratio difference in expression = 0.53). Overall, our results indicate that JUNB expression is downregulated in advanced phase CML through a mechanism independent from DNA methylation.

Indexed as

AnimalsCell Line, TumorDNA MethylationDNA PrimersDown-RegulationGene Expression Regulation, NeoplasticHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMiceMice, TransgenicNeoplasm StagingPolymerase Chain ReactionPromoter Regions, GeneticProto-Oncogene Proteins c-junRestriction MappingRNA, MessengerDNA PrimersProto-Oncogene Proteins c-junRNA, MessengerRNA, Neoplasm

Identifiers

PMID19409613
PMCPMC3833718
OpenAlexW1971592699

What OpenQuestion holds

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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.