Evidence map›Paper›PMID 29304017›Full record

ArticleSensors (Basel, Switzerland)2018

Genotyping of KRAS Mutational Status by the In-Check Lab-on-Chip Platform.

Maria Guarnaccia, Rosario Iemmolo, Floriana San Biagio, Enrico Alessi, Sebastiano Cavallaro

Open access · goldAbstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2018. 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
0.4field-weighted citation impact, top 36% 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, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

5 authors at 2 institutions in 1 country.

Maria GuarnacciaInstitute of Neurological Sciences, Italian National Research Council, Via Paolo Gaifami 18, 95126 Catania, Italy. maria.guarnaccia@cnr.it.
Rosario IemmoloInstitute of Neurological Sciences, Italian National Research Council, Via Paolo Gaifami 18, 95126 Catania, Italy. iemmolo.rosario@gmail.com.ORCID 0000-0002-9297-8115
Floriana San BiagioSTMicroelectronics, Stradale Primosole 50, 95121 Catania, Italy. floriana.sanbiagio@st.com.
Enrico AlessiAnalog, MEMS & Sensor Group-HealthCare Business Development Unit, STMicroelectronics, Stradale Primosole 50, 95121 Catania, Italy. enrico.alessi@st.com.ORCID 0000-0002-5710-2636
Sebastiano CavallaroInstitute of Neurological Sciences, Italian National Research Council, Via Paolo Gaifami 18, 95126 Catania, Italy. sebastiano.cavallaro@cnr.it.ORCID 0000-0001-7590-1792
Institute of Neurological Sciences · ITSTMicroelectronics (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The KRAS oncogene is involved in the pathogenesis of several types of cancer, particularly colorectal cancer (CRC). The most frequent mutations in this gene are associated with poor survival, increased tumor aggressiveness and resistance to therapy with anti-epidermal growth factor receptor (EGFR) antibodies. For this reason, KRAS mutation testing has become increasingly common in clinical practice for personalized cancer treatments of CRC patients. Detection methods for KRAS mutations are currently expensive, laborious, time-consuming and often lack of diagnostic sensitivity and specificity. In this study, we describe the development of a Lab-on-Chip assay for genotyping of KRAS mutational status. This assay, based on the In-Check platform, integrates microfluidic handling, a multiplex polymerase chain reaction (PCR) and a low-density microarray. This integrated sample-to-result system enables the detection of KRAS point mutations, including those occurring in codons 12 and 13 of exon 2, 59 and 61 of exon 3, 117 and 146 of exon 4. Thanks to its miniaturization, automation, rapid analysis, minimal risk of sample contamination, increased accuracy and reproducibility of results, this Lab-on-Chip platform may offer immediate opportunities to simplify KRAS genotyping into clinical routine.

Indexed as

Colorectal NeoplasmsDNA Mutational AnalysisGenotypeHumansMutationProto-Oncogene Proteins p21(ras)Reproducibility of ResultsKRAS protein, humanProto-Oncogene Proteins p21(ras)diagnosticKRASLab-on-ChipMicroarraynucleic acids analysisPCR

Identifiers

PMID29304017
PMCPMC5795341
OpenAlexW2783865703

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.