Evidence map›Paper›PMID 20473389›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2010

Microfluidic electroporation of tumor and blood cells: observation of nucleus expansion and implications on selective analysis and purging of circulating tumor cells.

Ning Bao, Thuc T Le, Ji-Xin Cheng, Chang Lu

Open access · greenAbstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
8.4field-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

22 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
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  6. Impact of Pulsed Electric Field Ablation on His Bundle Conduction: A Preclinical Canine Study.Medical science monitor : international medical journal of experimental and clinical research · 2024
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  14. Shape-dependent optoelectronic cell lysis.Angewandte Chemie (International ed. in English) · 2014
    Article
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  16. Article
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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

4 authors at 3 institutions in 2 countries.

Ning BaoDepartment of Agricultural and Biological Engineering, Purdue University, 225 S. University Street, West Lafayette, Indiana 47907, USA.
Thuc T Le
Ji-Xin Cheng
Chang Lu
Purdue University West Lafayette · USIn-Q-Tel · USNantong University · CN

Funding

Nonlinear Optical Imaging to Evaluate Obesity Associated Health RisksF32HL089074 · NHLBI · PURDUE UNIVERSITY · PI LE, THUC TRONG · 2007 to 2009
$148k
NHLBI NIH HHS F32 HL089074
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) refer to cells that detach from a primary tumor, circulate in the blood stream, and may settle down at a secondary site and form metastases. The detection and characterization of CTCs are clinically useful for diagnosis and prognosis purposes. However, there has been very little work on purging CTCs from the blood. In this study, we systematically studied electroporation of tumor and blood cells in the context of selective purging and analysis of CTCs, using M109 and mouse blood cells as models. Electroporation is a simple and effective method for disruption of the cell membrane by applying an external electric field. We applied a microfluidic flow-through electroporation to process cells with various electroporation durations and field intensities. With duration of 100-300 ms, we found that the thresholds for electroporation-induced lysis started at 300-400 V cm(-1) for M109, 400-500 V cm(-1) for white blood cells and 1100-1200 V cm(-1) for red blood cells. Due to the substantial difference, we demonstrated the selective electroporation of tumor cells among blood cells and the scale-up of the flow-through electroporation devices for processing samples of millilitre volumes. Using Coherent Anti-stokes Raman Scattering (CARS) and fluorescence microscopy tools, we observed the dramatic increase in the size of the nucleus of a tumor cell in response to the applied field. We suggest that the nucleus expansion is a newly discovered mechanism responsible for rapid tumor cell death resulted from electroporation.

Indexed as

AnimalsBlood CellsCell FractionationCell NucleusCell SeparationElectroporationEquipment DesignEquipment Failure AnalysisHumansMiceMicrofluidic Analytical TechniquesNeoplasmsNeoplastic Cells, Circulating

Identifiers

PMID20473389
PMCPMC2872780
OpenAlexW2132597046

What OpenQuestion holds

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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.