Evidence map›Paper›PMID 22341213›Full record

ArticleBiomaterials2012

The impact of adhesion peptides within hydrogels on the phenotype and signaling of normal and cancerous mammary epithelial cells.

Michael S Weiss, Beatriz Peñalver Bernabé, Ariella Shikanov, Dennis A Bluver, Michael D Mui, Seungjin Shin, Linda J Broadbelt, Lonnie D Shea

Abstract read
In one paragraph

Article in Biomaterials, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

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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 1 institution in 1 country.

Michael S WeissDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208-3120, USA.
Beatriz Peñalver Bernabé
Ariella Shikanov
Dennis A Bluver
Michael D Mui
Seungjin Shin
Linda J Broadbelt
Lonnie D Shea
Northwestern University · US

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
U54: The Oncofertility Consortium: Fertility Preservation for Woman (1 of 10)UL1DE019587 · NIDCR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WOODRUFF, TERESA K · 2008 to 2011
$3.7M
P30A: Biomaterials Core (6 of 10)PL1EB008542 · NIBIB · NORTHWESTERN UNIVERSITY · PI SHEA, LONNIE D · 2007 to 2011
$2.3M
Transfected cell arrays for cancer researchR21CA125285 · NCI · NORTHWESTERN UNIVERSITY · PI SHEA, LONNIE D · 2007 to 2008
$328k
NCI NIH HHS R21 CA125285NCI NIH HHS R21CA125285NIBIB NIH HHS PL1 EB008542NIBIB NIH HHS PL1EB008542NIDCR NIH HHS UL1 DE019587NIDCR NIH HHS UL1DE019587NIGMS NIH HHS P50 GM081892NIGMS NIH HHS T32 GM008449NIGMS NIH HHS T32GM008449
6 · The paper itself

Abstract

The microenviroment contributes to directing mammary epithelial cell (MEC) development and the progression of breast cancer. Three-dimensional culture models have been used to support formation of structures that display varying degrees of disorganization that parallel the degree of cancer. Synthetic hydrogels were employed to investigate the mechanisms by which specific adhesion signals in the microenvironment directed development. Polyethylene glycol-based hydrogels supported 3D growth of MECs and directed formation of a range of phenotypes that were functions of genotype, and identity and concentration of adhesion peptides RGD and YIGSR. Non-cancerous and cancerous MECs responded differentially to the same adhesion cues and produced variable structural organizations. An analysis of dynamic signaling pathways revealed differential activities of transcription factors within the MAPK and JAK/STAT pathways in response to genotype and adhesion. These results directly implicate adhesion in cancer development and demonstrate that AP1, CREB, STAT1, and STAT3 all contribute to the genotype dependence of cellular response to adhesion peptides. The tools presented in this work could be applied to other systems and connect extracellular cues with intracellular signaling to molecularly dissect tissue development and further biomaterials development.

Indexed as

Amino Acid SequenceBreast NeoplasmsCell AdhesionCell Line, TumorCell SurvivalEpithelial CellsFemaleHumansHydrogelsMammary Glands, HumanMolecular Sequence DataPeptidesPhenotypePolyethylene GlycolsRegression AnalysisSignal TransductionHydrogelsPeptidesPolyethylene Glycols

Identifiers

PMID22341213
PMCPMC3288720
OpenAlexW2074023684

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.