Evidence map›Paper›PMID 19636063›Full record

ArticleBlood2009

A pluripotency signature predicts histologic transformation and influences survival in follicular lymphoma patients.

Andrew J Gentles, Ash A Alizadeh, Su-In Lee, June H Myklebust, Catherine M Shachaf, Babak Shahbaba, Ronald Levy, Daphne Koller, Sylvia K Plevritis

Open access · greenAbstract 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 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

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  19. Identifying Network Perturbation in Cancer.PLoS computational biology · 2016
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Andrew J GentlesDepartment of Radiology, Stanford University School of Medicine, Lucas Center for MR Spectroscopy and Imaging, Stanford, CA 94305, USA. andrewg@stanford.edu
Ash A Alizadeh
Su-In Lee
June H Myklebust
Catherine M Shachaf
Babak Shahbaba
Ronald Levy
Daphne Koller
Sylvia K Plevritis
Stanford University · USUniversity of California, Irvine · US

Funding

TRIGGERING CELL DEATH IN B CELL LYMPHOMAP01CA034233 · NCI · STANFORD UNIVERSITY · PI FELSHER, DEAN W · 1985 to 2010
$19.5M
Computational Modeling of Cancer BiologyU56CA112973 · NCI · STANFORD UNIVERSITY · PI PLEVRITIS, SYLVIA KATINA · 2004 to 2009
$2.9M
NCI NIH HHS P01 CA034233NCI NIH HHS P01-CA34233NCI NIH HHS U56 CA112973NCI NIH HHS U56CA112973
6 · The paper itself

Abstract

Histologic transformation (HT) of follicular lymphoma to diffuse large B-cell lymphoma (DLBCL-t) is associated with accelerated disease course and drastically worse outcome, yet the underlying mechanisms are poorly understood. We show that a network of gene transcriptional modules underlies HT. Central to the network hierarchy is a signature strikingly enriched for pluripotency-related genes. These genes are typically expressed in embryonic stem cells (ESCs), including MYC and its direct targets. This core ESC-like program was independent of proliferation/cell-cycle and overlapped but was distinct from normal B-cell transcriptional programs. Furthermore, we show that the ESC program is correlated with transcriptional programs maintaining tumor phenotype in transgenic MYC-driven mouse models of lymphoma. Although our approach was to identify HT mechanisms rather than to derive an optimal survival predictor, a model based on ESC/differentiation programs stratified patient outcomes in 2 independent patient cohorts and was predictive of propensity of follicular lymphoma tumors to transform. Transformation was associated with an expression signature combining high expression of ESC transcriptional programs with reduced expression of stromal programs. Together, these findings suggest a central role for an ESC-like signature in the mechanism of HT and provide new clues for potential therapeutic targets.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell CycleCell DifferentiationDisease Models, AnimalEmbryonic Stem CellsFemaleHumansLymphoma, FollicularLymphoma, Large B-Cell, DiffuseMaleMiceMice, TransgenicPluripotent Stem CellsProto-Oncogene Proteins c-mycTranscription, GeneticProto-Oncogene Proteins c-myc

Identifiers

PMID19636063
PMCPMC2759646
OpenAlexW2100640770

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.