Evidence map›Paper›PMID 34663896›Full record

ArticleScientific reports2021

Negative enrichment of circulating tumor cells from unmanipulated whole blood with a 3D printed device.

Chia-Heng Chu, Ruxiu Liu, Tevhide Ozkaya-Ahmadov, Brandi E Swain, Mert Boya, Bassel El-Rayes, Mehmet Akce, Mehmet Asim Bilen, Omer Kucuk, A Fatih Sarioglu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 11 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

10 authors at 2 institutions in 1 country.

Chia-Heng ChuSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, USA.
Ruxiu LiuSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, USA.
Tevhide Ozkaya-AhmadovSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, USA.
Brandi E SwainSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, USA.
Mert BoyaSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, USA.
Bassel El-RayesWinship Cancer Institute, Emory University, Atlanta, USA.
Mehmet AkceWinship Cancer Institute, Emory University, Atlanta, USA.
Mehmet Asim BilenWinship Cancer Institute, Emory University, Atlanta, USA.
Omer KucukWinship Cancer Institute, Emory University, Atlanta, USA.
A Fatih SariogluSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, USA. sarioglu@gatech.edu.
Emory University · USGeorgia Institute of Technology · US

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
NCI NIH HHS P30 CA138292NIH HHS P30CA138292
6 · The paper itself

Abstract

Reliable and routine isolation of circulating tumor cells (CTCs) from peripheral blood would allow effective monitoring of the disease and guide the development of personalized treatments. Negative enrichment of CTCs by depleting normal blood cells ensures against a biased selection of a subpopulation and allows the assay to be applied on different tumor types. Here, we report an additively manufactured microfluidic device that can negatively enrich viable CTCs from clinically-relevant volumes of unmanipulated whole blood samples. Our device depletes nucleated blood cells based on their surface antigens and the smaller anucleated cells based on their size. Enriched CTCs are made available off the device in suspension making our technique compatible with standard immunocytochemical, molecular and functional assays. Our device could achieve a ~ 2.34-log depletion by capturing > 99.5% of white blood cells from 10 mL of whole blood while recovering > 90% of spiked tumor cells. Furthermore, we demonstrated the capability of the device to isolate CTCs from blood samples collected from patients (n = 15) with prostate and pancreatic cancers in a pilot study. A universal CTC assay that can differentiate tumor cells from normal blood cells with the specificity of clinically established membrane antigens yet require no label has the potential to enable routine blood-based tumor biopsies at the point-of-care.

Indexed as

AdultAgedCell CountCell Line, TumorCell SeparationFemaleHumansLab-On-A-Chip DevicesLeukocytesMaleMicrofluidic Analytical TechniquesMiddle AgedNeoplastic Cells, CirculatingPilot ProjectsPrinting, Three-Dimensional

Identifiers

PMID34663896
PMCPMC8523721
OpenAlexW3207330440

What OpenQuestion holds

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LicenceCC BY
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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.