Evidence map›Paper›PMID 16293596›Full record

ArticleBlood2006

A MAPK/HNRPK pathway controls BCR/ABL oncogenic potential by regulating MYC mRNA translation.

Mario Notari, Paolo Neviani, Ramasamy Santhanam, Bradley W Blaser, Ji-Suk Chang, Annamaria Galietta, Anne E Willis, Denis C Roy, Michael A Caligiuri, Guido Marcucci and 1 more

Open access · greenAbstract read
In one paragraph

Article in Blood, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

106 citing papers in PubMed, 214 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. ELP3 stabilizes c-Myc to promote tumorigenesis.Journal of molecular cell biology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Article
  12. Article
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  14. The Role of RNA-Binding Proteins in Hematological Malignancies.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

46 more citing papers are in PubMed but not listed here.

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

11 authors at 1 institution in 1 country.

Mario NotariHuman Cancer Genetics Program, The Ohio State University Medical Center, Columbus, OH 43240, USA.
Paolo Neviani
Ramasamy Santhanam
Bradley W Blaser
Ji-Suk Chang
Annamaria Galietta
Anne E Willis
Denis C Roy
Michael A Caligiuri
Guido Marcucci
Danilo Perrotti
Cancer Genetics (United States) · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Role of RNA-Binding Proteins in BCR/ABL LeukemogenesisR01CA095512 · NCI · OHIO STATE UNIVERSITY · PI PERROTTI, DANILO · 2003 to 2012
$2.2M
NCI NIH HHS CA095512NCI NIH HHS CA16058NCI NIH HHS R01 CA095512
6 · The paper itself

Abstract

Altered mRNA translation is one of the effects exerted by the BCR/ABL oncoprotein in the blast crisis phase of chronic myelogenous leukemia (CML). Here, we report that in BCR/ABL+ cell lines and in patient-derived CML blast crisis mononuclear and CD34+ cells, p210(BCR/ABL) increases expression and activity of the transcriptional-inducer and translational-regulator heterogeneous nuclear ribonucleoprotein K (hnRNP K or HNRPK) in a dose- and kinase-dependent manner through the activation of the MAPK(ERK1/2) pathway. Furthermore, HNRPK down-regulation and interference with HNRPK translation-but not transcription-regulatory activity impairs cytokine-independent proliferation, clonogenic potential, and in vivo leukemogenic activity of BCR/ABL-expressing myeloid 32Dcl3 and/or primary CD34+ CML-BC patient cells. Mechanistically, we demonstrate that decreased internal ribosome entry site (IRES)-dependent Myc mRNA translation accounts for the phenotypic changes induced by inhibition of the BCR/ABL-ERK-dependent HNRPK translation-regulatory function. Accordingly, MYC protein but not mRNA levels are increased in the CD34+ fraction of patients with CML in accelerated and blastic phase but not in chronic phase CML patients and in the CD34+ fraction of marrow cells from healthy donors. Thus, BCR/ABL-dependent enhancement of HNRPK translation-regulation is important for BCR/ABL leukemogenesis and, perhaps, it might contribute to blast crisis transformation.

Indexed as

Protein BiosynthesisAntigens, CD34Blast CrisisCell Line, TumorFusion Proteins, bcr-ablHeterogeneous-Nuclear Ribonucleoprotein KHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMitogen-Activated Protein KinasesProto-Oncogene Proteins c-mycRibonucleoproteinsRNA, MessengerTumor Cells, CulturedAntigens, CD34Fusion Proteins, bcr-ablHeterogeneous-Nuclear Ribonucleoprotein KHNRNPK protein, humanMitogen-Activated Protein KinasesMYC protein, humanProto-Oncogene Proteins c-mycRibonucleoproteinsRNA, Messenger

Identifiers

PMID16293596
PMCPMC1895740
OpenAlexW2166830325

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.