Evidence map›Paper›PMID 36332335›Full record

ArticleBiosensors & bioelectronics2023

miRNA probe integrated biosensor platform using bimetallic nanostars for amplification-free multiplexed detection of circulating colorectal cancer biomarkers in clinical samples.

Aidan J Canning, Xinrong Chen, Joy Q Li, William R Jeck, Hsin-Neng Wang, Tuan Vo-Dinh

Open access · greenAbstract read
In one paragraph

Article in Biosensors & bioelectronics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 39 citations in OpenAlex.

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  11. An Acoustofluidic Picoinjector.Sensors and actuators. B, Chemical · 2024
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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

6 authors at 2 institutions in 1 country.

Aidan J CanningFitzpatrick Institute for Photonics, Duke University, Durham, NC, 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
Xinrong ChenDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
Joy Q LiFitzpatrick Institute for Photonics, Duke University, Durham, NC, 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
William R JeckDepartment of Pathology, Duke University Medical Center, Durham, NC, 27708, USA; Duke Cancer Institute, Duke School of Medicine, Durham, NC, 27708, USA.
Hsin-Neng WangFitzpatrick Institute for Photonics, Duke University, Durham, NC, 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
Tuan Vo-DinhFitzpatrick Institute for Photonics, Duke University, Durham, NC, 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC, 27708, USA; Department of Chemistry, Duke University, Durham, NC, 27708, USA; Duke Cancer Institute, Duke School of Medicine, Durham, NC, 27708, USA. Electronic address: tuan.vodinh@duke.edu.
Duke University · USDuke Cancer Institute

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI Laura Fish · 1985 to 2026
$174.8M
Integrated Acoustofluidic Plasmonic Molecular Diagnostic System for Detecting MicroRNA BiomarkersR01GM135486 · NIGMS · DUKE UNIVERSITY · PI VO-DINH, TUAN · 2020 to 2023
$1.8M
NCI NIH HHS P30 CA014236NIGMS NIH HHS R01 GM135486
6 · The paper itself

Abstract

There is a critical need for sensitive and rapid detection technologies utilizing molecular biotargets such as microRNAs (miRNAs), which regulate gene expression and are a promising class of diagnostic biomarkers for disease detection. Here, we present the development and fabrication of a highly reproducible and robust plasmonic bimetallic nanostar biosensing platform to detect miRNA targets using surfaced-enhanced Raman scattering (SERS)-based gene probes called the inverse Molecular Sentinel (iMS). We investigated and optimized the integration of iMS gene probes onto this SERS substrate, achieving ultra-sensitive detection with limits of detection of 6.8 and 16.7 zmol within the sensing region for two miRNA sequences of interest. Finally, we demonstrated the biomedical usefulness of this nanobiosensor platform with the multiplexed detection of upregulated miRNA targets, miR21 and miR221, from colorectal cancer patient plasma. The resulting SERS data are in excellent agreement with PCR data obtained from patient samples and can distinguish between healthy and cancerous patient samples. These results underline the potential of the iMS-integrated substrate nanobiosensing platform for rapid and sensitive diagnostics of cancer biomarkers for point-of-care applications.

Indexed as

Biosensing TechniquesColorectal NeoplasmsMetal NanoparticlesMicroRNAsBiomarkers, TumorGoldHumansLimit of DetectionSpectrum Analysis, RamanBiomarkers, TumorGoldMicroRNAsMIRN21 microRNA, humanBiosensorEarly detectionmiRNA detectionPlasmonic nanoparticleSERS Substrate

Identifiers

PMID36332335
PMCPMC9881606
OpenAlexW4308039007

What Socratic 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 Socratic graph.