Evidence map›Paper›PMID 32627398›Full record

ArticleAdvanced biosystems2019

Analyzing Mechanisms of Metastatic Cancer Cell Adhesive Phenotype Leveraging Preparative Adhesion Chromatography Microfluidic.

Katherine G Birmingham, Meghan J O'Melia, Dongjo Ban, Janna Mouw, Erin E Edwards, Adam I Marcus, John McDonald, Susan N Thomas

Abstract read
In one paragraph

Article in Advanced biosystems, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Targeting CD24 as a novel immunotherapy for solid cancers.Cell communication and signaling : CCS · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cell Separations and Sorting.Analytical chemistry · 2020
    Review
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.

Katherine G BirminghamGeorge W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, 30332, USA.ORCID 0000-0002-7802-7516
Meghan J O'MeliaWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, 30332, USA.ORCID 0000-0003-2223-1849
Dongjo BanSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Janna MouwWinship Cancer Institute, Emory University, Atlanta, GA, 30322, USA.
Erin E EdwardsParker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Adam I MarcusWinship Cancer Institute, Emory University, Atlanta, GA, 30322, USA.
John McDonaldParker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, 30332, USA.ORCID 0000-0002-4263-8155
Susan N ThomasGeorge W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, 30332, USA.ORCID 0000-0003-4651-232X

Funding

Research Training Program Plan on Cell and Tissue Engineering (CTEng)T32GM008433 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 1991 to 2021
$7.1M
uSHEAR Technology for Cancer Cell PurificaitonR21CA202849 · NCI · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J, THOMAS, SUSAN NAPIER · 2016 to 2018
$600k
NCI NIH HHS R21 CA202849NIGMS NIH HHS T32 GM008433NIH HHS R21 CA202849NIH HHS T32 GM-008433
6 · The paper itself

Abstract

An integrated, parallel-plate microfluidic device is engineered to interrogate and fractionate cells based on their adhesivity to a substrate surface functionalized with adhesive ligand in a tightly controlled flow environment to elucidate associated cell-intrinsic pathways. Wall shear stress levels and endothelial presentation of E-selectin are modeled after the inflamed vasculature microenvironment in order to simulate in vitro conditions under which in vivo hematogenous metastasis occurs. Based on elution time from the flow channel, the collection of separate fractions of cells-noninteracting and interacting-at high yields and viabilities enables multiple postperfusion analyses, including flow cytometry, in vivo metastasis modeling, and transcriptomic analysis. This platform enables the interrogation of flow-regulated cell molecular profiles, such as (co)expression levels of natively expressed selectin ligands sLe

Indexed as

Cell Adhesion MoleculesAnimalsCell AdhesionCell Line, TumorChromatographyColonic NeoplasmsEquipment DesignE-SelectinHumansMiceMice, SCIDMicrofluidic Analytical TechniquesNeoplasm MetastasisPhenotypeCell Adhesion MoleculesE-SelectinSELE protein, humancolon cancerE-selectinmetastasismicrofluidicsialyl Lewis x

Identifiers

PMID32627398
PMCPMC7657380

What Socratic 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 Socratic graph.