Evidence map›Paper›PMID 36758042›Full record

ArticlePloS one2023

Detection of BRAF mutations in malignant melanoma and colorectal cancer by SensiScreen® FFPE BRAF qPCR assay.

Anna Lahn Sørensen, Mariann Guldmann-Christensen, Michael Børgesen, Rasmus Koefoed Petersen, Katharina Flugt, Julie Mejer Holmgaard Duelund, Majbritt Hauge Kyneb, Jan Lorenzen, Emma Pipó-Ollé, Samantha Epistolio and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 99% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

16 authors at 3 institutions in 2 countries.

Anna Lahn SørensenPentaBase A/S, Odense, Denmark.ORCID 0000-0001-9002-8995
Mariann Guldmann-ChristensenDepartment of Pathology, Laboratory of Research and Development, Aarhus University Hospital, Aarhus, Denmark.
Michael BørgesenPentaBase A/S, Odense, Denmark.
Rasmus Koefoed PetersenPentaBase A/S, Odense, Denmark.
Katharina FlugtPentaBase A/S, Odense, Denmark.
Julie Mejer Holmgaard DuelundDepartment of Pathology, Laboratory of Research and Development, Aarhus University Hospital, Aarhus, Denmark.
Majbritt Hauge KynebDanish Technological Institute, Aarhus, Denmark.
Jan LorenzenDanish Technological Institute, Aarhus, Denmark.
Emma Pipó-OlléPentaBase A/S, Odense, Denmark.
Samantha EpistolioInstitute of Pathology EOC, Ente Ospedaliero Cantonale, Locarno, Switzerland.ORCID 0000-0003-1236-2722
Alice RivaInstitute of Pathology EOC, Ente Ospedaliero Cantonale, Locarno, Switzerland.
Giulia DazioInstitute of Pathology EOC, Ente Ospedaliero Cantonale, Locarno, Switzerland.
Elisabetta MerloInstitute of Pathology EOC, Ente Ospedaliero Cantonale, Locarno, Switzerland.
Tine MeyerDepartment of Pathology, Laboratory of Research and Development, Aarhus University Hospital, Aarhus, Denmark.
Ulf Bech ChristensenPentaBase A/S, Odense, Denmark.
Milo FrattiniInstitute of Pathology EOC, Ente Ospedaliero Cantonale, Locarno, Switzerland.
Ente Ospedaliero Cantonale · CHAarhus University Hospital · DKDanish Technological Institute · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in BRAF exon 15 lead to conformational changes in its activation loops, resulting in constitutively active BRAF proteins which are implicated in the development of several human cancer types. Different BRAF inhibitors have been developed and introduced in clinical practice. Identification of BRAF mutations influences the clinical evaluation, treatment, progression and for that reason a sensitive and specific identification of BRAF mutations is on request from the clinic. Here we present the SensiScreen® FFPE BRAF qPCR Assay that uses a novel real-time PCR-based method for BRAF mutation detection based on PentaBases proprietary DNA analogue technology designed to work on standard real-time PCR instruments. The SensiScreen® FFPE BRAF qPCR Assay displays high sensitivity, specificity, fast and easy-to-use. The SensiScreen® FFPE BRAF qPCR Assay was validated on two different FFPE tumour biopsy cohorts, one cohort included malignant melanoma patients previously analyzed by the Cobas® 4800 BRAF V600 Mutation Test, and one cohort from colorectal cancer patients previously analyzed by mutant-enriched PCR and direct sequencing. All BRAF mutant malignant melanoma patients were confirmed with the SensiScreen® FFPE BRAF qPCR Assay and additional four new mutations in the malignant melanoma cohort were identified. All the previously identified BRAF mutations in the colorectal cancer patients were confirmed, and additional three new mutations not identified with direct sequencing were detected. Also, one new BRAF mutation not previously identified with ME-PCR was found. Furthermore, the SensiScreen® FFPE BRAF qPCR Assay identified the specific change in the amino acid. The SensiScreen® FFPE BRAF qPCR Assay will contribute to a more specific, time and cost saving approach to better identify and characterize mutations in patients affected by cancer, and consequently permits a better BRAF characterization that is fundamental for therapy decision.

Indexed as

Colorectal NeoplasmsMelanomaCutaneous Malignant MelanomaDNA Mutational AnalysisHumansMutationProto-Oncogene Proteins B-rafReal-Time Polymerase Chain ReactionBRAF protein, humanProto-Oncogene Proteins B-raf

Identifiers

PMID36758042
PMCPMC9910728
OpenAlexW4319655900

What OpenQuestion holds

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LicenceCC BY
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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.