Evidence map›Paper›PMID 31792349›Full record

ArticleBritish journal of cancer2020

Quantification of HER1, HER2 and HER3 by time-resolved Förster resonance energy transfer in FFPE triple-negative breast cancer samples.

Alexandre Ho-Pun-Cheung, Hervé Bazin, Florence Boissière-Michot, Caroline Mollevi, Joëlle Simony-Lafontaine, Emeline Landas, Jean-Pierre Bleuse, Thierry Chardès, Jean-François Prost, André Pèlegrin and 3 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Advances in PET/CT Imaging for Breast Cancer.Journal of clinical medicine · 2023
    Review
  6. Review
  7. Article
  8. Article
  9. The Radiolabeled HER3 Targeting Molecules for Tumor Imaging.Iranian journal of pharmaceutical research : IJPR · 2021
    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

13 authors at 5 institutions in 1 country.

Alexandre Ho-Pun-CheungICM, Institut régional du Cancer de Montpellier, Montpellier, France.
Hervé BazinCisBio SA, Codolet, France.
Florence Boissière-MichotICM, Institut régional du Cancer de Montpellier, Montpellier, France.
Caroline MolleviICM, Institut régional du Cancer de Montpellier, Montpellier, France.
Joëlle Simony-LafontaineICM, Institut régional du Cancer de Montpellier, Montpellier, France.
Emeline LandasCisBio SA, Codolet, France.
Jean-Pierre BleuseICM, Institut régional du Cancer de Montpellier, Montpellier, France.
Thierry ChardèsInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM, Université de Montpellier, Institut régional du Cancer de Montpellier (ICM), Montpellier, France.
Jean-François ProstGamaMabs Pharma SA, Centre Pierre Potier, Toulouse, France.
André PèlegrinInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM, Université de Montpellier, Institut régional du Cancer de Montpellier (ICM), Montpellier, France.
William JacotICM, Institut régional du Cancer de Montpellier, Montpellier, France.
Gérard MathisCisBio SA, Codolet, France.
Evelyne Lopez-CrapezICM, Institut régional du Cancer de Montpellier, Montpellier, France. evelyne.crapez@icm.unicancer.fr.
Cisbio (France) · FRInstitut de Recherche en Cancérologie de Montpellier · FRInstitut Regional du Cancer de MontpellierUniversité de Montpellier · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) has a worse prognosis compared with other breast cancer subtypes, and biomarkers to identify patients at high risk of recurrence are needed. Here, we investigated the expression of human epidermal receptor (HER) family members in TNBC and evaluated their potential as biomarkers of recurrence.

methodsWe developed Time Resolved-Förster Resonance Energy Transfer (TR-FRET) assays to quantify HER1, HER2 and HER3 in formalin-fixed paraffin-embedded (FFPE) tumour tissues. After assessing the performance and precision of our assays, we quantified HER protein expression in 51 TNBC specimens, and investigated the association of their expression with relapse-free survival.

resultsThe assays were quantitative, accurate, and robust. In TNBC specimens, HER1 levels ranged from ≈4000 to more than 2 million receptors per cell, whereas HER2 levels varied from ≈1000 to 60,000 receptors per cell. HER3 expression was very low (less than 5500 receptors per cell in all samples). Moderate HER2 expression was significantly associated with higher risk of recurrence (HR = 3.93; P = 0.003).

conclusionsOur TR-FRET assays accurately quantify HER1, HER2 and HER3 in FFPE breast tumour specimens. Moderate HER2 expression may represent a novel prognostic marker in patients with TNBC.

Indexed as

AdultAgedAged, 80 and overCarcinoma, Ductal, BreastDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleFluorescence Resonance Energy TransferHumansImmunohistochemistryMiddle AgedNeoplasm Recurrence, LocalPrognosisReceptor, ErbB-3Triple Negative Breast NeoplasmsEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesERBB3 protein, humanErbB ReceptorsReceptor, ErbB-3

Identifiers

PMID31792349
PMCPMC7000684
OpenAlexW2991100602

What OpenQuestion holds

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LicenceCC BY
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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.