Evidence map›Paper›PMID 32923312›Full record

ArticleNanotheranostics2020

Multiplex detection of ctDNA mutations in plasma of colorectal cancer patients by PCR/SERS assay.

Nana Lyu, Vinoth Kumar Rajendran, Russell J Diefenbach, Kellie Charles, Stephen J Clarke, Alexander Engel, Sydney 1000 Colorectal Cancer Study Investigators*, Helen Rizos, Mark P Molloy, Yuling Wang

Open access · goldAbstract read
In one paragraph

Article in Nanotheranostics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 39 citations in OpenAlex.

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  13. Current status of ctDNA in precision oncology for hepatocellular carcinoma.Journal of experimental & clinical cancer research : CR · 2021
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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

10 authors at 5 institutions in 1 country.

Nana LyuDepartment of Molecular Sciences, Macquarie University, Sydney, Australia.
Vinoth Kumar RajendranDepartment of Molecular Sciences, Macquarie University, Sydney, Australia.
Russell J DiefenbachDepartment of Biomedical Sciences, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, Australia.
Kellie CharlesSchool of Medical Sciences, Discipline of Pharmacology, The University of Sydney, Australia.
Stephen J ClarkeRoyal North Shore Hospital, Department of Medical Oncology, The University of Sydney, Australia.
Alexander EngelRoyal North Shore Hospital, Colorectal Surgical Unit, The University of Sydney, Australia.
Sydney 1000 Colorectal Cancer Study Investigators*
Helen RizosDepartment of Biomedical Sciences, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, Australia.
Mark P MolloyBowel Cancer and Biomarker Laboratory, Kolling Institute, The University of Sydney, Australia.
Yuling WangDepartment of Molecular Sciences, Macquarie University, Sydney, Australia.
Macquarie University · AURoyal North Shore Hospital · AUThe University of Sydney · AUCancer Institute of New South Wales · AUMelanoma Institute Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular diagnostic testing of KRAS and BRAF mutations has become critical in the management of colorectal cancer (CRC) patients. Some progress has been made in liquid biopsy detection of mutations in circulating tumor DNA (ctDNA), which is a fraction of circulating cell-free DNA (cfDNA), but slow analysis for DNA sequencing methods has limited rapid diagnostics. Other methods such as quantitative PCR and more recently, droplet digital PCR (ddPCR), have limitations in multiplexed capacity and the need for expensive specialized equipment. Hence, a robust, rapid and facile strategy is needed for detecting multiple ctDNA mutations to improve the management of CRC patients. To address this significant problem, herein, we propose a new application of multiplex PCR/SERS (surface-enhanced Raman scattering) assay for the detection of ctDNA in CRC, in a fast and non-invasive manner to diagnose and stratify patients for effective treatment.

Indexed as

Colorectal NeoplasmsCirculating Tumor DNAHCT116 CellsHumansLiquid BiopsyMultiplex Polymerase Chain ReactionMutationSensitivity and SpecificitySpectrum Analysis, RamanCirculating Tumor DNACRCctDNAddPCRmultiplex detectionPCR/SERS assay

Identifiers

PMID32923312
PMCPMC7484630
OpenAlexW3082448482

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.