Evidence map›Paper›PMID 34561533›Full record

ArticleCommunications biology2021

Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device.

Jose Montoya Mira, Ajay A Sapre, Brett S Walker, Jesus Bueno Alvarez, Kyle T Gustafson, Eugene Tu, Jared M Fischer, Melissa H Wong, Sadik Esener, Yu-Jui Chiu

Abstract read
In one paragraph

Article in Communications biology, 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
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. [Recent advances in responsive isolation, release and clinical application of circulating tumor cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. 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

10 authors.

Jose Montoya Mira *Knight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA.
Ajay A Sapre *Knight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA.
Brett S WalkerDepartment of Surgery, Oregon Health & Science University, Portland, OR, 97239, USA.
Jesus Bueno AlvarezKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA.
Kyle T GustafsonKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA.
Eugene TuKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA.
Jared M FischerKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA.ORCID http://orcid.org/0000-0002-0062-0870
Melissa H WongThe Knight Cancer Institute, Oregon Health & Science University, Portland, OR, 97201, USA.
Sadik EsenerKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA.ORCID http://orcid.org/0000-0002-6873-0478
Yu-Jui ChiuKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, Portland, OR, 97201, USA. chiuyu@ohsu.edu.ORCID http://orcid.org/0000-0002-5382-106X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular circulating biomarkers from the primary tumor such as circulating tumor cells (CTCs) and circulating hybrid cells (CHCs) have been described to harbor tumor-like phenotype and genotype. CHCs are present in higher numbers than CTCs supporting their translational potential. Methods for isolation of CHCs do not exist and are restricted to low-throughput, time consuming, and biased methodologies. We report the development of a label-free dielectrophoretic microfluidic platform facilitating enrichment of CHCs in a high-throughput and rapid fashion by depleting healthy peripheral blood mononuclear cells (PBMCs). We demonstrated up to 96.5% depletion of PBMCs resulting in 18.6-fold enrichment of cancer cells. In PBMCs from pancreatic adenocarcinoma patients, the platform enriched neoplastic cells identified by their KRAS mutant status using droplet digital PCR with one hour of processing. Enrichment was achieved in 75% of the clinical samples analyzed, establishing this approach as a promising way to non-invasively analyze tumor cells from patients.

Indexed as

Biomarkers, TumorEquipment DesignHumansLab-On-A-Chip DevicesLeukocytes, MononuclearMCF-7 CellsMedical OncologyNeoplastic Cells, CirculatingBiomarkers, Tumor

Identifiers

PMID34561533
PMCPMC8463600

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.