Evidence map›Paper›PMID 19520806›Full record

ArticleBlood2009

Src homology 2 domain-containing inositol-5-phosphatase and CCAAT enhancer-binding protein beta are targeted by miR-155 in B cells of Emicro-MiR-155 transgenic mice.

Stefan Costinean, Sukhinder K Sandhu, Irene M Pedersen, Esmerina Tili, Rossana Trotta, Danilo Perrotti, David Ciarlariello, Paolo Neviani, Jason Harb, Lauren Rachel Kauffman and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 160 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed, 1 pooled it
11.3field-weighted citation impact, top 1% 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

160 citing papers in PubMed, 1 synthesis or guideline pooled it, 287 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Review
  7. Exosomal microRNA as a key regulator of PI3K/AKT pathways in human tumors.Medical oncology (Northwood, London, England) · 2024
    Review
  8. Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Review
  10. Article
  11. MicroRNA-regulated B cells in obesity.Immunometabolism (Cobham, Surrey) · 2022
    Review
  12. Generation of MiRNA sponge constructs targeting multiple MiRNAs.Journal of clinical laboratory analysis · 2022
    Article
  13. Review
  14. Pathway Analysis for Cancer Research and Precision Oncology Applications.Advances in experimental medicine and biology · 2022
    Article
  15. Review
  16. Review
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  19. Review
  20. Article

100 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

12 authors at 2 institutions in 1 country.

Stefan CostineanComprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Sukhinder K Sandhu
Irene M Pedersen
Esmerina Tili
Rossana Trotta
Danilo Perrotti
David Ciarlariello
Paolo Neviani
Jason Harb
Lauren Rachel Kauffman
Aaditya Shidham
Carlo Maria Croce
The Ohio State University · USUniversity of California, San Diego · US

Funding

Role of miR155 in LeukemogenesisR01CA124541 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2008 to 2012
$1.8M
NCI NIH HHS 5R01CA124541NCI NIH HHS R01 CA124541
6 · The paper itself

Abstract

We showed that Emicro-MiR-155 transgenic mice develop acute lymphoblastic leukemia/high-grade lymphoma. Most of these leukemias start at approximately 9 months irrespective of the mouse strain. They are preceded by a polyclonal pre-B-cell proliferation, have variable clinical presentation, are transplantable, and develop oligo/monoclonal expansion. In this study, we show that in these transgenic mice the B-cell precursors have the highest MiR-155 transgene expression and are at the origin of the leukemias. We determine that Src homology 2 domain-containing inositol-5-phosphatase (SHIP) and CCAAT enhancer-binding protein beta (C/EBPbeta), 2 important regulators of the interleukin-6 signaling pathway, are direct targets of MiR-155 and become gradually more down-regulated in the leukemic than in the preleukemic mice. We hypothesize that miR-155, by down-modulating Ship and C/EBPbeta, initiates a chain of events that leads to the accumulation of large pre-B cells and acute lymphoblastic leukemia/high-grade lymphoma.

Indexed as

AnimalsCCAAT-Enhancer-Binding Protein-betaCell Transformation, NeoplasticDown-RegulationGene Expression Regulation, LeukemicInositol Polyphosphate 5-PhosphatasesInterleukin-6Lymphoma, B-CellMiceMice, TransgenicMicroRNAsPhosphoric Monoester HydrolasesPrecursor Cell Lymphoblastic Leukemia-LymphomaPrecursor Cells, B-LymphoidSignal TransductionCCAAT-Enhancer-Binding Protein-betaInositol Polyphosphate 5-PhosphatasesInterleukin-6MicroRNAsMirn155 microRNA, mousePhosphoric Monoester Hydrolases

Identifiers

PMID19520806
PMCPMC2727407
OpenAlexW2072076620

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.