Evidence map›Paper›PMID 24077027›Full record

ArticleNature nanotechnology2013

Sensitive capture of circulating tumour cells by functionalized graphene oxide nanosheets.

Hyeun Joong Yoon, Tae Hyun Kim, Zhuo Zhang, Ebrahim Azizi, Trinh M Pham, Costanza Paoletti, Jules Lin, Nithya Ramnath, Max S Wicha, Daniel F Hayes and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature nanotechnology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 168 papers.

0numbers the graph read from it
0cells of the map it votes in
168citing papers in PubMed
30.9field-weighted citation impact, top 1% 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

168 citing papers in PubMed, 531 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
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  7. Review
  8. Article
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  11. Article
  12. Article
  13. Review
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108 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Hyeun Joong YoonDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Tae Hyun Kim
Zhuo Zhang
Ebrahim Azizi
Trinh M Pham
Costanza Paoletti
Jules Lin
Nithya Ramnath
Max S Wicha
Daniel F Hayes
Diane M Simeone
Sunitha Nagrath
University of Michigan–Ann Arbor · USMichigan Center for Translational Pathology · US

Funding

ZINC GLUCONATE GLYCINE LOZENGES &VITAMIN C EFFECTS ON COMMON COLDM01RR000042 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ORAL, ELIF ARIOGLU · 1985 to 2007
$40.8M
Translational Research in GI CancerP50CA130810 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BRENNER, DEAN E. · 2010 to 2016
$11.8M
Engineering sensitive microfluidic multiplex technology for isolating circulatingDP2OD006672 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NAGRATH, SUNITHA · 2009 to 2009
$2.1M
NCI NIH HHS CA130810NCI NIH HHS P50 CA130810NCRR NIH HHS M01 RR000042NIH HHS 1DP2OD006672-01NIH HHS DP2 OD006672
6 · The paper itself

Abstract

The spread of cancer throughout the body is driven by circulating tumour cells (CTCs). These cells detach from the primary tumour and move from the bloodstream to a new site of subsequent tumour growth. They also carry information about the primary tumour and have the potential to be valuable biomarkers for disease diagnosis and progression, and for the molecular characterization of certain biological properties of the tumour. However, the limited sensitivity and specificity of current methods for measuring and studying these cells in patient blood samples prevents the realization of their full clinical potential. The use of microfluidic devices is a promising method for isolating CTCs. However, the devices are reliant on three-dimensional structures, which limits further characterization and expansion of cells on the chip. Here we demonstrate an effective approach to isolating CTCs from blood samples of pancreatic, breast and lung cancer patients, by using functionalized graphene oxide nanosheets on a patterned gold surface. CTCs were captured with high sensitivity at a low concentration of target cells (73 ± 32.4% at 3-5 cells per ml blood).

Indexed as

Neoplastic Cells, CirculatingBiomarkers, TumorBreast NeoplasmsCell Line, TumorCell SeparationFemaleGraphiteHumansLung NeoplasmsMCF-7 CellsMicrofluidic Analytical TechniquesNanostructuresPancreatic NeoplasmsSensitivity and SpecificityBiomarkers, TumorGraphite

Identifiers

PMID24077027
PMCPMC4017624
OpenAlexW1986688132

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.