Evidence map›Paper›PMID 30430922›Full record

ArticleTissue engineering. Part C, Methods2019

A High-Throughput Workflow to Study Remodeling of Extracellular Matrix-Based Microtissues.

Katherine A Cummins, Alexandra L Crampton, David K Wood

Erratum issuedAbstract read
In one paragraph

Article in Tissue engineering. Part C, Methods, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Katherine A CumminsDepartment of Biomedical Engineering, University of Minnesota-Twin Cities, Minneapolis, Minnesota.
Alexandra L CramptonDepartment of Biomedical Engineering, University of Minnesota-Twin Cities, Minneapolis, Minnesota.
David K WoodDepartment of Biomedical Engineering, University of Minnesota-Twin Cities, Minneapolis, Minnesota.

Funding

Matrix remodeling in microfluidic co-cultureR21HL132256 · NHLBI · MAYO CLINIC ROCHESTER · PI TSCHUMPERLIN, DANIEL J. · 2016 to 2017
$443k
Functionally maturing iPSC-derived human hepatocytes in 3D microgelsR21ES027622 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KHETANI, SALMAN R · 2017 to 2018
$427k
NHLBI NIH HHS R21 HL132256NIEHS NIH HHS R21 ES027622
6 · The paper itself

Abstract

impact statementThe described microtissue-microwell workflow is uniquely suited for high-throughput study of extracellular matrix (ECM) remodeling at the molecular, cellular, and tissue levels and demonstrates possibilities of studying progressive, heterogeneous diseases in a way that is meaningful for drug discovery and development. We outline several assays that can be utilized in studying tissue-level diseases and functions that involve cell-ECM interactions and ECM remodeling (e.g., cancer, fibrosis, wound healing) in pursuit of an improved three-dimensional cell culturing system. Finally, we demonstrate the ability to cryopreserve cells encapsulated in microtissue constructs while remaining highly viable, proliferative, and retaining cell functions that are involved in ECM remodeling.

Indexed as

Cell ProliferationCells, CulturedExtracellular MatrixExtracellular Matrix ProteinsFibroblastsHumansHuman Umbilical Vein Endothelial CellsTissue EngineeringWorkflowExtracellular Matrix Proteins3D cell culturedropletsECM remodelinghigh-throughput screeningmicrofluidicsmicrotissues

Identifiers

PMID30430922
PMCPMC6352510

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.