Evidence map›Paper›PMID 33042766›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2020

Dual-Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity-Based Microfluidic Interfaces.

Yoon-Tae Kang, Thomas Hadlock, Ting-Wen Lo, Emma Purcell, Anusha Mutukuri, Shamileh Fouladdel, Monica De Silva Raguera, Heather Fairbairn, Vasudha Murlidhar, Alison Durham and 2 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

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  20. Plasmon-Enhanced Single Extracellular Vesicle Analysis for Cholangiocarcinoma Diagnosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    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

12 authors.

Yoon-Tae KangDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.ORCID https://orcid.org/0000-0003-1596-7815
Thomas HadlockDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.ORCID https://orcid.org/0000-0002-9123-4982
Ting-Wen LoDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Emma PurcellDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Anusha MutukuriDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Shamileh FouladdelDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Monica De Silva RagueraDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Heather FairbairnDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Vasudha MurlidharDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.
Alison DurhamUniversity of Michigan-Michigan Medicine 1910 Taubman Center 1500 E. Medical Center Drive Ann Arbor MI 48109 USA.
Scott A McLeanRoger Cancer Center University of Michigan 1500 E Medical Center Ann Arbor 48109 USA.
Sunitha NagrathDepartment of Chemical Engineering and Biointerface Institute University of Michigan 2800 Plymouth Road, NCRC B10-A184 Ann Arbor MI 48109 USA.ORCID https://orcid.org/0000-0002-1497-7977

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is among the most aggressive cancers, and its rate of incidence continues to grow. Early detection of melanoma has been hampered due to the lack of promising markers for testing. Recent advances in liquid biopsy have proposed noninvasive alternatives for cancer diagnosis and monitoring. Circulating tumor cells (CTCs) and cancer-exosomes are gaining influence as promising biomarkers because of their cancer-associated molecular markers and signatures. However, technologies that offer the dual-isolation of CTCs and exosomes using a single sample have not been thoroughly developed. The dual-utilization OncoBean (DUO) device is conjugated with melanoma specific antibodies, MCAM and MCSP, enabling simultaneous CTC and exosome isolations. Using blood samples from patients, CTCs and exosomes are specifically isolated from a single sample and then undergo molecular profiling for comprehensive study. Melanoma patients have 0-17CTCs mL

Indexed as

circulating tumor cellsdual isolation and profilingmelanomamicrofluidicstumor exosomes

Identifiers

PMID33042766
PMCPMC7539202

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Registered trials

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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.