Evidence map›Paper›PMID 26783561›Full record

ArticleThe Analyst2016

Amplification-free in situ KRAS point mutation detection at 60 copies per mL in urine in a background of 1000-fold wild type.

Ceyhun E Kirimli, Wei-Heng Shih, Wan Y Shih

Open access · greenAbstract read
In one paragraph

Article in The Analyst, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. 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

3 authors at 1 institution in 1 country.

Ceyhun E KirimliDrexel University, School of Biomedical Engineering, Science, and Health Systems, Philadelphia, Pennsylvania 19104, USA. shihwy@drexel.edu.
Wei-Heng ShihDrexel University, Department of Materials Science and Engineering, Philadelphia, Pennsylvania, USA.
Wan Y ShihDrexel University, School of Biomedical Engineering, Science, and Health Systems, Philadelphia, Pennsylvania 19104, USA. shihwy@drexel.edu.
Drexel University · US

Funding

Rapid, Accurate, and Low-Cost Stool Clostridium difficile Genetic TestR41AI112224 · NIAID · LENIMA FIELD DIAGNOSTICS, LLC · PI SHIH, WAN Y. · 2014 to 2014
$300k
A Low-Cost Portable Multiplex Serum Molecular Test for HBV and HCV DetectionR41AI120445 · NIAID · LENIMA FIELD DIAGNOSTICS, LLC · PI SHIH, WAN Y. · 2015 to 2015
$300k
NIAID NIH HHS 1R41AI112224NIAID NIH HHS 1R41AI120445NIAID NIH HHS R41 AI112224NIAID NIH HHS R41 AI120445
6 · The paper itself

Abstract

We have examined the in situ detection of a single-nucleotide KRAS mutation in urine using a (Pb(Mg1/3Nb2/3)O3)0.65(PbTiO3)0.35 (PMN-PT) piezoelectric plate sensor (PEPS) coated with a 17-nucleotide (nt) locked nucleic acid (LNA) probe DNA complementary to the KRAS mutation. To enhance the in situ mutant (MT) DNA detection specificity against the wild type (WT), detection was carried out in a flow with a flow rate of 4 mL min(-1) and at 63 °C with the PEPS vertically situated at the center of the flow in which both the temperature and the flow impingement force discriminated the wild type. Under such conditions, PEPS was shown to specifically detect KRAS MT in situ with 60 copies per mL analytical sensitivity in a background of clinically-relevant 1000-fold more WT in 30 min without DNA isolation, amplification, or labeling. For validation, this detection was followed with detection in a mixture of blue MT fluorescent reporter microspheres (FRMs) (MT FRMs) that bound to only the captured MT and orange WT FRMs that bound to only the captured WT. Microscopic examinations showed that the captured blue MT FRMs still outnumbered the orange WT FRMs by a factor of 4 to 1 even though WT was 1000-fold of MT in urine. Finally, multiplexed specific mutation detection was demonstrated using a 6-PEPS array each with a probe DNA targeting one of the 6 codon-12 KRAS mutations.

Indexed as

Point MutationPolymorphism, Single NucleotideBase SequenceBiosensing TechniquesHumansOligonucleotide ProbesOligonucleotidesProto-Oncogene Proteins p21(ras)KRAS protein, humanlocked nucleic acidOligonucleotide ProbesOligonucleotidesProto-Oncogene Proteins p21(ras)

Identifiers

PMID26783561
PMCPMC4747796
OpenAlexW2229396125

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.