Evidence map›Paper›PMID 32381091›Full record

ArticleJournal of nanobiotechnology2020

Negative depletion mediated brightfield circulating tumour cell identification strategy on microparticle-based microfluidic chip.

Shuibing Wang, Shaoli Hong, Shijia Cai, Jia Lei, Jinyao Chen, Nangang Zhang, Zhao Ai, Kan Liu, Man Tang

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Application of Microfluidics in Detection of Circulating Tumor Cells.Frontiers in bioengineering and biotechnology · 2022
    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

9 authors at 1 institution in 1 country.

Shuibing WangSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.
Shaoli HongSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.
Shijia CaiSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.
Jia LeiSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.
Jinyao ChenSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.
Nangang ZhangSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.
Zhao AiSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China.
Kan LiuSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China. liukan2002@gmail.com.
Man TangSchool of Electronic and Electrical Engineering, Wuhan Textile University, Wuhan, 430200, People's Republic of China. mtang@wtu.edu.cn.ORCID http://orcid.org/0000-0002-6821-5986
Wuhan Textile University · CN

Funding

National Natural Science Foundation of China 81372358National Natural Science Foundation of China 81527801
6 · The paper itself

Abstract

backgroundThe most convenient circulating tumor cells (CTCs) identification method is direct analysis of cells under bright field microscopy by which CTCs can be comprehensive studied based on morphology, phenotype or even cellular function. However, universal cell markers and a standard tumour cell map do not exist, thus limiting the clinical application of CTCs.

resultsThis paper focuses on an automatic and convenient negative depletion strategy for circulating tumour cell identification under bright field microscopy. In this strategy, immune microparticles (IMPs) are applied to negatively label white blood cells rather than the tumour cells, such that tumour cells can be directly distinguished under brightfield of the microscopy. In this way, all of the heterogeneous tumour cells and their phenotype properties can be retained for further cancer-related studies. In addition, a wedge-shaped microfluidic chip is constructed for heterogeneous CTC pre-purification and enrichment by size, thus significantly decreasing the interference of haematological cells. Additionally, all cell treatments are processed automatically, and the tumour cells can be rapidly counted and distinguished via customized cell analytical software, showing high detection efficiency and automation. This IMPs based negative cell labelling strategy can also be combined with other classic cell identification methods, thus demonstrating its excellent compatibility.

conclusionThis identification strategy features simple and harmless for tumour cells, as well as excellent accuracy and efficiency. And the low equipment demand and high automation level make it promise for extensive application in basic medical institutions.

Indexed as

Lab-On-A-Chip DevicesCell Line, TumorCell SeparationEquipment DesignHumansNeoplastic Cells, CirculatingBrightfieldCirculating tumour cellIdentificationMicrofluidic chipNegative depletion

Identifiers

PMID32381091
PMCPMC7206695
OpenAlexW3023015082

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.