Evidence map›Paper›PMID 28636636›Full record

ArticlePloS one2017

SensiScreen®KRAS exon 2-sensitive simplex and multiplex real-time PCR-based assays for detection of KRAS exon 2 mutations.

Alice Riva, Michael BØrgesen, Mariann Guldmann-Christensen, Majbritt Hauge Kyneb, Kirsten Voogd, Christina Andersen, Samantha Epistolio, Elisabetta Merlo, Tine Yding Wolff, Stephen Hamilton-Dutoit and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 55% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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 2 institutions in 1 country.

Alice RivaLaboratory of Molecular Pathology, Institute of Pathology, Locarno, Switzerland.
Michael BØrgesenPentaBase Aps, Odense, Denmark.
Mariann Guldmann-ChristensenLaboratory of Research and Development, Department of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Majbritt Hauge KynebLife Science Division, Danish Technological Institute, Aarhus, Denmark.
Kirsten VoogdLaboratory of Research and Development, Department of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Christina AndersenPentaBase Aps, Odense, Denmark.
Samantha EpistolioLaboratory of Molecular Pathology, Institute of Pathology, Locarno, Switzerland.
Elisabetta MerloLaboratory of Molecular Pathology, Institute of Pathology, Locarno, Switzerland.
Tine Yding WolffLife Science Division, Danish Technological Institute, Aarhus, Denmark.
Stephen Hamilton-DutoitLaboratory of Research and Development, Department of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Jan LorenzenLife Science Division, Danish Technological Institute, Aarhus, Denmark.
Ulf Bech ChristensenPentaBase Aps, Odense, Denmark.
Milo FrattiniLaboratory of Molecular Pathology, Institute of Pathology, Locarno, Switzerland.ORCID http://orcid.org/0000-0003-2334-3412
Aarhus University Hospital · DKDanish Technological Institute · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activating mutations in codon 12 and codon 13 of the KRAS (Kirsten rat sarcoma viral oncogene homolog) gene are implicated in the development of several human cancer types and influence their clinical evaluation, treatment and prognosis. Numerous different methods for KRAS genotyping are currently available displaying a wide range of sensitivities, time to answer and requirements for laboratory equipment and user skills. Here we present SensiScreen® KRAS exon 2 simplex and multiplex CE IVD assays, that use a novel real-time PCR-based method for KRAS mutation detection based on PentaBase's proprietary DNA analogue technology and designed to work on standard real-time PCR instruments. By means of the included BaseBlocker™ technology, we show that SensiScreen® specifically amplifies the mutated alleles of interest with no or highly subdued amplification of the wild type allele. Furthermore, serial dilutions of mutant DNA in a wild type background demonstrate that all SensiScreen® assays display a limit of detection that falls within the range of 0.25-1%. Finally, in three different colorectal cancer patient populations, SensiScreen® assays confirmed the KRAS genotype previously determined by commonly used methods for KRAS mutation testing, and notably, in two of the populations, SensiScreen® identified additional mutant positive cases not detected by common methods.

Indexed as

ExonsBiological AssayCohort StudiesColorectal NeoplasmsDNA, NeoplasmGenotypeHumansMultiplex Polymerase Chain ReactionMutationProto-Oncogene Proteins p21(ras)Real-Time Polymerase Chain ReactionTumor Cells, CulturedDNA, NeoplasmKRAS protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID28636636
PMCPMC5479524
OpenAlexW2697066943

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.