Evidence map›Paper›PMID 20812256›Full record

ArticleBiotechnology and bioengineering2011

Cellular arrays for large-scale analysis of transcription factor activity.

Abigail D Bellis, Beatriz Peňalver-Bernabé, Michael S Weiss, Michael E Yarrington, Maria V Barbolina, Angela K Pannier, Jacqueline S Jeruss, Linda J Broadbelt, Lonnie D Shea

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  13. Lentiviral arrays for live-cell dynamic monitoring of gene and pathway activity during stem cell differentiation.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
  14. Article
  15. Article
  16. Transcription factor networks in invasion-promoting breast carcinoma-associated fibroblasts.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2013
    Article
  17. Article
  18. Article
  19. 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

9 authors at 3 institutions in 1 country.

Abigail D BellisDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208-3120, USA.
Beatriz Peňalver-Bernabé
Michael S Weiss
Michael E Yarrington
Maria V Barbolina
Angela K Pannier
Jacqueline S Jeruss
Linda J Broadbelt
Lonnie D Shea
Northwestern University · USUniversity of Illinois Chicago · USUniversity of Nebraska–Lincoln · US

Funding

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
The Oncogenic Significance of Cyclin Overexpression and Smad 3 Tumor SuppressionK22CA138776 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JERUSS, JACQUELINE SARA · 2010 to 2012
$561k
Transfected cell arrays for cancer researchR21CA125285 · NCI · NORTHWESTERN UNIVERSITY · PI SHEA, LONNIE D · 2007 to 2008
$328k
NCI NIH HHS K22 CA138776NCI NIH HHS R21 CA125285NIGMS NIH HHS T32 GM008449PHS HHS R21 006520
6 · The paper itself

Abstract

Identifying molecular mechanisms or therapeutic targets is typically based on large-scale cellular analysis that measures the abundance of mRNA or protein; however, abundance does not necessarily correlate with activity. We report a method for direct large-scale quantification of active pathways that employs a cellular array with parallel gene delivery of constructs that report pathway activity. The reporter constructs encode luciferase, whose expression is influenced by binding of transcription factors (TFs), which are the downstream targets of signaling pathways. Luciferase levels are quantified by bioluminescence imaging (BLI), which allows for rapid, non-invasive measurements. Activity profiles by BLI of 32 TFs were robust, consistent, and reproducible, and correlated with standard cell lysis techniques. The array identified five TFs with differential activity during phorbol-12-myristate-13-acetate (PMA)-induced differentiation of breast cancer cells. A system for rapid, large-scale, BLI quantification of pathway activity provides an enabling technology for mechanistic studies of cellular responses and processes.

Indexed as

Gene Expression ProfilingMicroarray AnalysisGene Expression RegulationGenes, ReporterLuciferasesLuminescent MeasurementsMetabolic Networks and PathwaysTranscription FactorsLuciferasesTranscription Factors

Identifiers

PMID20812256
PMCPMC3022829
OpenAlexW2128187647

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.