Evidence map›Paper›PMID 18922927›Full record

ArticleCancer research2008

Utilization of pathway signatures to reveal distinct types of B lymphoma in the Emicro-myc model and human diffuse large B-cell lymphoma.

Seiichi Mori, Rachel E Rempel, Jeffrey T Chang, Guang Yao, Anand S Lagoo, Anil Potti, Andrea Bild, Joseph R Nevins

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

50 citing papers in PubMed, 72 citations in OpenAlex.

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  18. Uncovering the Role of RNA-Binding Protein hnRNP K in B-Cell Lymphomas.Journal of the National Cancer Institute · 2020
    Article
  19. Eμ-TCL1xMyc: A Novel Mouse Model for Concurrent CLL and B-Cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    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

8 authors at 2 institutions in 1 country.

Seiichi MoriDepartment of Molecular Genetics and Microbiology, Duke Institute for Genome Sciences and Policy, Duke University Medical Center, Durham, North Carolina 27708, USA.
Rachel E Rempel
Jeffrey T Chang
Guang Yao
Anand S Lagoo
Anil Potti
Andrea Bild
Joseph R Nevins
Duke Medical Center · USUniversity of Utah · US

Funding

Integration of Oncogenic Networks in Cancer PhenotypesU54CA112952 · NCI · DUKE UNIVERSITY · PI NEVINS, JOSEPH R · 2004 to 2009
$12.4M
Oncogenic Gene Regulatory NetworksR01CA106520 · NCI · DUKE UNIVERSITY · PI CHI, JEN-TSAN ASHLEY · 2005 to 2014
$2.9M
Functional Components of the Rb/E2F and p53 PathwaysR00LM009837 · NLM · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHANG, JEFFREY T · 2010 to 2012
$699k
Functional Components of the Rb/E2F and p53 PathwaysK99LM009837 · NLM · DUKE UNIVERSITY · PI CHANG, JEFFREY T · 2008 to 2009
$180k
NCI NIH HHS R01 CA106520NCI NIH HHS R01CA106520NCI NIH HHS U54 CA112952NCI NIH HHS U54CA112952NLM NIH HHS K99 LM009837NLM NIH HHS R00 LM009837
6 · The paper itself

Abstract

The Emu-myc transgenic mouse has provided a valuable model for the study of B-cell lymphoma. Making use of gene expression analysis and, in particular, expression signatures of cell signaling pathway activation, we now show that several forms of B lymphoma can be identified in the Emu-myc mice associated with time of tumor onset. Furthermore, one form of Emu-myc tumor with pre-B character is shown to resemble human Burkitt lymphoma, whereas others exhibit more differentiated B-cell characteristics and show similarity with human diffuse large B-cell lymphoma in the pattern of gene expression, as well as oncogenic pathway activation. Importantly, we show that signatures of oncogenic pathway activity provide further dissection of the spectrum of diffuse large B-cell lymphoma, identifying a subset of patients who have very poor prognosis and could benefit from more aggressive or novel therapeutic strategies. Taken together, these studies provide insight into the complexity of the oncogenic process and a novel strategy for dissecting the heterogeneity of B lymphoma.

Indexed as

Disease Models, AnimalGene Expression ProfilingGenes, mycAnimalsHumansLymphoma, B-CellLymphoma, Large B-Cell, DiffuseMiceMice, Inbred C57BLMice, TransgenicPrognosisSignal TransductionTime Factors

Identifiers

PMID18922927
PMCPMC3617051
OpenAlexW2129757408

What OpenQuestion holds

Textmetadata
LicenceTDM
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.