Evidence map›Paper›PMID 30259795›Full record

ArticleTissue engineering. Part A2019

Extracellular Matrix Degradation Products Downregulate Neoplastic Esophageal Cell Phenotype.

Lindsey T Saldin, Shil Patel, Li Zhang, Luai Huleihel, George S Hussey, David G Nascari, Lina M Quijano, Xue Li, Divya Raghu, Anant K Bajwa and 8 more

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 8 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

18 authors at 4 institutions in 1 country.

Lindsey T Saldin1 Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.
Shil Patel2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Li Zhang2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Luai Huleihel2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
George S Hussey2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
David G Nascari2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Lina M Quijano2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Xue Li2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Divya Raghu2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Anant K Bajwa1 Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.
Nicholas G Smith2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Christopher C Chung2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Ashten N Omstead3 Esophageal and Lung Institute, Allegheny Health Network, Pittsburgh, Pennsylvania.
Juliann E Kosovec3 Esophageal and Lung Institute, Allegheny Health Network, Pittsburgh, Pennsylvania.
Blair A Jobe3 Esophageal and Lung Institute, Allegheny Health Network, Pittsburgh, Pennsylvania.
Neill J Turner2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Ali H Zaidi3 Esophageal and Lung Institute, Allegheny Health Network, Pittsburgh, Pennsylvania.
Stephen F Badylak2 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
McGowan Institute for Regenerative Medicine · USUniversity of Pittsburgh · USAllegheny Health Network · USLung Institute · US

Funding

Understanding Esophageal Adenocarcinoma Progression Using Inflammatory and Neoplastic Extracellular Matrix HydrogelsF31CA210694 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SALDIN, LINDSEY T. · 2016 to 2017
$80k
NCI NIH HHS F31 CA210694
6 · The paper itself

Abstract

impact statementExtracellular matrix (ECM) biomaterials were used to treat esophageal cancer patients after cancer resection and promoted regrowth of normal mucosa without recurrence of cancer. The present study investigates the mechanisms by which these materials were successful to prevent the cancerous phenotype. ECM downregulated neoplastic esophageal cell function (proliferation, metabolism), but normal esophageal epithelial cells were unaffected

Indexed as

Down-RegulationAnimalsApoptosisAutophagyCell CycleCell Line, TumorCell ProliferationCell ShapeDNA ReplicationEsophageal NeoplasmsExtracellular MatrixGene Expression Regulation, NeoplasticHumansPhenotypePhosphatidylinositol 3-KinasesPhosphorylationPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktcell/matrix interactiondynamic reciprocityesophageal cancerextracellular matrix bioscaffoldgene expression

Identifiers

PMID30259795
PMCPMC6450457
OpenAlexW2893789215

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.