Evidence map›Paper›PMID 23947293›Full record

ArticleAnalytical chemistry2013

Modular microsystem for the isolation, enumeration, and phenotyping of circulating tumor cells in patients with pancreatic cancer.

J W Kamande, M L Hupert, M A Witek, H Wang, R J Torphy, U Dharmasiri, S K Njoroge, J M Jackson, R D Aufforth, A Snavely and 2 more

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 108 citations in OpenAlex.

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  14. Microfluidic gasketless interconnects sealed by superhydrophobic surfaces.Journal of microelectromechanical systems : a joint IEEE and ASME publication on microstructures, microactuators, microsensors, and microsystems · 2020
    Article
  15. An integrated, optofluidic system with aligned optical waveguides, microlenses, and coupling prisms for fluorescence sensing.Journal of microelectromechanical systems : a joint IEEE and ASME publication on microstructures, microactuators, microsensors, and microsystems · 2020
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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

12 authors at 4 institutions in 2 countries.

J W KamandeDepartment of Chemistry, Louisiana State University , 232 Choppin Hall, Baton Rouge, Louisiana 70803-1804, United States.
M L Hupert
M A Witek
H Wang
R J Torphy
U Dharmasiri
S K Njoroge
J M Jackson
R D Aufforth
A Snavely
J J Yeh
S A Soper
University of North Carolina at Chapel Hill · USBioFluidica (United States) · USUNC Lineberger Comprehensive Cancer CenterLouisiana State University · US

Funding

spFRET for Expression Profiling mRNA: Discovering Markers for Stroke DiagnosisR01EB010087 · NIBIB · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI BAIRD, ALISON E, SOPER, STEVEN ALLAN · 2011 to 2014
$2.5M
Acute Myeloid Leukemia: MRD Analysis Using Modular uFluidics and uFlow CytometryR21CA173279 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SOPER, STEVEN ALLAN · 2013 to 2015
$757k
NCI NIH HHS HHSN261201000066CNCI NIH HHS HHSN261201000066INCI NIH HHS N43CO-2010-00066NCI NIH HHS R21 CA173279NIBIB NIH HHS R01 EB010087NIBIB NIH HHS R01-EB010087
6 · The paper itself

Abstract

In this manuscript, we discuss the development and clinical use of a thermoplastic modular microsystem for the high-throughput analysis of CTCs directly from whole blood. The modular system offers some innovative features that address challenges currently associated with many CTC platforms; it can exhaustively process 7.5 mL of blood in less than 45 min with recoveries >90%. In addition, the system automates the postselection CTC processing steps and thus, significantly reduces assay turnaround time (from selection to enumeration <1.5 h as compared to >8 h for many reported CTC platforms). The system is composed of 3 functional modules including (i) a thermoplastic CTC selection module composed of high aspect ratio (30 μm × 150 μm) channels containing anti-EpCAM antibodies that is scalable in terms of throughput by employing channel numbers ranging from 50 to 320; the channel number is user selected to accommodate the volume of blood that must be processed; (ii) an impedance sensor module for label-less CTC counting; and (iii) a staining and imaging module for the placement of released cells into a 2D array within a common imaging plane for phenotypic identification. To demonstrate the utility of this system, blood samples from patients with local resectable and metastatic pancreatic ductal adenocarcinoma (PDAC) were analyzed. We demonstrate the ability to select EpCAM positive CTCs from PDAC patients in high purity (>86%) and with excellent yields (mean = 53 CTCs per mL for metastatic PDAC patients) using our modular system. In addition, we demonstrate the ability to detect CTCs in PDAC patients with local resectable disease (mean = 11 CTCs per mL).

Indexed as

Microfluidic Analytical TechniquesCell SeparationHumansNeoplastic Cells, CirculatingPancreatic NeoplasmsPhenotypeTumor Cells, Cultured

Identifiers

PMID23947293
PMCPMC3832346
OpenAlexW2047936820

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.