Evidence map›Paper›PMID 27892928›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2017

Microfluidics-assisted fluorescence in situ hybridization for advantageous human epidermal growth factor receptor 2 assessment in breast cancer.

Huu Tuan Nguyen, Raphaël Trouillon, Seiya Matsuoka, Maryse Fiche, Laurence de Leval, Bettina Bisig, Martin Am Gijs

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Microfluidics combined with fluorescenceFrontiers in bioengineering and biotechnology · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Rapid micro fluorescenceBiomicrofluidics · 2018
    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

7 authors at 2 institutions in 1 country.

Huu Tuan NguyenLaboratory of Microsystems 2, École Polytechnique Fédérale de Lausanne EPFL, Lausanne, Switzerland.ORCID 0000-0001-6130-2828
Raphaël TrouillonLaboratory of Microsystems 2, École Polytechnique Fédérale de Lausanne EPFL, Lausanne, Switzerland.
Seiya MatsuokaLaboratory of Microsystems 2, École Polytechnique Fédérale de Lausanne EPFL, Lausanne, Switzerland.
Maryse FicheInstitute of Pathology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
Laurence de LevalInstitute of Pathology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
Bettina BisigInstitute of Pathology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
Martin Am GijsLaboratory of Microsystems 2, École Polytechnique Fédérale de Lausanne EPFL, Lausanne, Switzerland.
École Polytechnique Fédérale de Lausanne · CHUniversity Hospital of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence in situ hybridization (FISH) is one of the recommended techniques for human epidermal growth factor receptor 2 (HER2) status assessment on cancer tissues. Here we develop microfluidics-assisted FISH (MA-FISH), in which hybridization of the FISH probes with their target DNA strands is obtained by applying square-wave oscillatory flows of diluted probe solutions in a thin microfluidic chamber of 5 μl volume. By optimizing the experimental parameters, MA-FISH decreases the consumption of the expensive probe solution by a factor 5 with respect to the standard technique, and reduces the hybridization time to 4 h, which is four times faster than in the standard protocol. To validate the method, we blindly conducted HER2 MA-FISH on 51 formalin-fixed paraffin-embedded tissue slides of 17 breast cancer samples, and compared the results with standard HER2 FISH testing. HER2 status classification was determined according to published guidelines, based on average number of HER2 copies per cell and average HER2/CEP17 ratio. Excellent agreement was observed between the two methods, supporting the validity of MA-FISH and further promoting its short hybridization time and reduced reagent consumption.

Indexed as

Breast NeoplasmsDNA ProbesErb-b2 Receptor Tyrosine KinasesFemaleGene DosageHumansIn Situ Hybridization, FluorescenceMicrofluidicsReproducibility of ResultsSensitivity and SpecificityTime FactorsDNA ProbesERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID27892928
OpenAlexW2559076955

What OpenQuestion holds

Textmetadata
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.