Evidence map›Paper›PMID 30511022›Full record

ArticleCommunications biology2018

RollFISH achieves robust quantification of single-molecule RNA biomarkers in paraffin-embedded tumor tissue samples.

Chenglin Wu, Michele Simonetti, Carla Rossell, Marco Mignardi, Reza Mirzazadeh, Laura Annaratone, Caterina Marchiò, Anna Sapino, Magda Bienko, Nicola Crosetto and 1 more

Abstract read
In one paragraph

Article in Communications biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Insights Into Spatial Transcriptomics: Exploring Recent Technical Developments and Their Diverse Applications.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
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  3. Spatial Proofreading Amplification ofbioRxiv : the preprint server for biology · 2025
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  5. Article
  6. Review
  7. Article
  8. Review
  9. The dawn of spatial omics.Science (New York, N.Y.) · 2023
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Engineered Tools to Study Intercellular Communication.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Guidelines for the Optimization and Validation of In Situ Hybridization.Methods in molecular biology (Clifton, N.J.) · 2020
    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

11 authors.

Chenglin Wu1Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.
Michele Simonetti2Science for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.
Carla Rossell2Science for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.
Marco Mignardi1Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.
Reza Mirzazadeh2Science for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.
Laura Annaratone3Department of Medical Sciences, University of Turin, Corso Dogliotti 14, 10126 Turin, Italy.ORCID 0000-0001-5750-1445
Caterina Marchiò3Department of Medical Sciences, University of Turin, Corso Dogliotti 14, 10126 Turin, Italy.
Anna Sapino3Department of Medical Sciences, University of Turin, Corso Dogliotti 14, 10126 Turin, Italy.
Magda Bienko2Science for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.ORCID 0000-0002-6499-9082
Nicola Crosetto2Science for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.
Mats Nilsson1Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Tomtebodavägen 23a, 17165 Solna, Stockholm Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-molecule RNA fluorescence in situ hybridization (smFISH) represents a promising approach to quantify the expression of clinically useful biomarkers in tumor samples. However, routine application of smFISH to formalin-fixed, paraffin-embedded (FFPE) samples is challenging due to the low signal intensity and high background noise. Here we present RollFISH, a method combining the specificity of smFISH with the signal boosting of rolling circle amplification. We apply RollFISH to quantify widely used breast cancer biomarkers in cell lines and FFPE samples. Thanks to the high signal-to-noise ratio, we can visualize selected biomarkers at low magnification (20 × ) across entire tissue sections, and thus assess their spatial heterogeneity. Lastly, we apply RollFISH to quantify HER2 mRNA in 150 samples on a single tissue microarray, achieving a sensitivity and specificity of detection of HER2-positive samples of ~90%. RollFISH is a robust method for quantifying the expression and intratumor heterogeneity of biomarkers in FFPE tissues.

Identifiers

PMID30511022
PMCPMC6262000

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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.