Evidence map›Paper›PMID 31767345›Full record

ArticleBiosensors & bioelectronics2020

Post-enrichment circulating tumor cell detection and enumeration via deformability impedance cytometry.

Parham Ghassemi, Xiang Ren, Brittni M Foster, Bethany A Kerr, Masoud Agah

Open access · greenAbstract read
In one paragraph

Article in Biosensors & bioelectronics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
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

5 authors at 2 institutions in 1 country.

Parham GhassemiThe Bradley Department of Electrical and Computer Engineering, Virginia Tech, Blacksburg, VA, 24061, United States. Electronic address: pghassem@vt.edu.
Xiang RenThe Bradley Department of Electrical and Computer Engineering, Virginia Tech, Blacksburg, VA, 24061, United States. Electronic address: xren@vt.edu.
Brittni M FosterDepartment of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, United States. Electronic address: bmfoster@wakehealth.edu.
Bethany A KerrDepartment of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, United States. Electronic address: bkerr@wakehealth.edu.
Masoud AgahThe Bradley Department of Electrical and Computer Engineering, Virginia Tech, Blacksburg, VA, 24061, United States. Electronic address: agah@vt.edu.
Virginia Tech · USWake Forest University · US

Funding

CD117 Signaling as a Mechanism of Prostate Cancer MetastasisR00CA175291 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KERR, BETHANY AMBER · 2016 to 2018
$722k
High Throughput Mechanical Modulatory Assay for Breast Cancer Drug TestingR21CA210126 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI AGAH, MASOUD · 2016 to 2017
$395k
NCI NIH HHS R00 CA175291NCI NIH HHS R21 CA210126
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) in blood can provide valuable information when detecting, diagnosing, and monitoring cancer. This paper describes a system that consists of a constriction-based microfluidic sensor with embedded electrodes that can detect and enumerate cancer cells in blood. The biosensor measures impedance in terms of magnitude and phase at multiple frequencies as cells transit through the constriction channel. Cancer cells deform as they move through while blood cells remain intact, thus generating differential impedance profiles that can be used for detecting and counting CTCs. Two versions of this device are reported, one where the electrodes are embedded into the disposable microfluidic channel, and the other in which the disposable chip is externally fixed to a reusable substrate housing the electrodes. Both configurations were tested by spiking breast or prostate cancer cells into murine blood, and both detected all tumor cells passing through the narrow channels while being able to differentiate between the two cell lines. The chip in its current format has a throughput of 1 μL/min. While the throughput is scalable by integrating more constriction channels in parallel, the presented assay is intended for post-enrichment label-free enumeration and characterization of CTCs.

Indexed as

Biosensing TechniquesCell CountCell Line, TumorCell SeparationElectric ImpedanceHumansMicrofluidic Analytical TechniquesNeoplasmsNeoplastic Cells, CirculatingCancerCirculating tumor cellsImpedanceLiquid biopsyMicrofluidics

Identifiers

PMID31767345
PMCPMC6957725
OpenAlexW2983920626

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.