Evidence map›Paper›PMID 25303361›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2014

Dynamic transcription factor activity and networks during ErbB2 breast oncogenesis and targeted therapy.

M S Weiss, B Peñalver Bernabé, S Shin, S Asztalos, S J Dubbury, M D Mui, A D Bellis, D Bluver, D A Tonetti, J Saez-Rodriguez and 3 more

Abstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

13 authors.

M S WeissChemical and Biological Engineering Department, Northwestern University, Evanston, IL, USA. l-shea@northwestern.edu j-jeruss@northwestern.edu broadbelt@northwestern.edu.
B Peñalver Bernabé
S Shin
S Asztalos
S J Dubbury
M D Mui
A D Bellis
D Bluver
D A Tonetti
J Saez-Rodriguez
L J Broadbelt
J S Jeruss
L D Shea

Funding

CORE: ADMINISTRATIVEP50GM081892 · NIGMS · UNIVERSITY OF CHICAGO · PI WHITE, KEVIN P. · 2008 to 2013
$15.9M
Developing Capacity to Evaluate Training Programs via Development of Human, Institutional and Social CapitalT32GM008449 · NIGMS · NORTHWESTERN UNIVERSITY · PI LEONARD, JOSHUA NATHANIEL · 1993 to 2023
$7.8M
An in vivo metastasis sensorR01CA173745 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BACKMAN, VADIM, SHEA, LONNIE D · 2012 to 2016
$4.2M
Measuring signaling pathway dynamics during tissue growth in hydrogelsR01GM097220 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JERUSS, JACQUELINE SARA, SHEA, LONNIE D · 2012 to 2015
$1.4M
NCI NIH HHS R01 CA173745NIGMS NIH HHS P50 GM081892NIGMS NIH HHS P50GM081892NIGMS NIH HHS R01 GM097220NIGMS NIH HHS R01GM097220NIGMS NIH HHS T32 GM008449NIGMS NIH HHS T32GM008449
6 · The paper itself

Abstract

Tissue development and disease progression are multi-stage processes controlled by an evolving set of key regulatory factors, and identifying these factors necessitates a dynamic analysis spanning relevant time scales. Current omics approaches depend on incomplete biological databases to identify critical cellular processes. Herein, we present TRACER (TRanscriptional Activity CEll aRrays), which was employed to quantify the dynamic activity of numerous transcription factor (TFs) simultaneously in 3D and networks for TRACER (NTRACER), a computational algorithm that allows for cellular rewiring to establish dynamic regulatory networks based on activity of TF reporter constructs. We identified major hubs at various stages of culture associated with normal and abnormal tissue growth (i.e., ELK-1 and E2F1, respectively) and the mechanism of action for a targeted therapeutic, lapatinib, through GATA-1, which were confirmed in human ErbB2 positive breast cancer patients and human ErbB2 positive breast cancer cell lines that were either sensitive or resistant to lapatinib.

Indexed as

Adaptor Proteins, Signal TransducingAntineoplastic AgentsBreast NeoplasmsCarcinogenesisCell Line, TumorCell SurvivalComputer SimulationFemaleHumansLapatinibModels, BiologicalMolecular Targeted TherapyProtein Array AnalysisQuinazolinesTranscriptional ActivationTranscription FactorsAdaptor Proteins, Signal TransducingAntineoplastic AgentsERBIN protein, humanLapatinibQuinazolinesTranscription Factors

Identifiers

PMID25303361
PMCPMC4237672

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.