Evidence map›Paper›PMID 30533973›Full record

ArticleSensors and actuators. B, Chemical2019

Microfluidic Exponential Rolling Circle Amplification for Sensitive microRNA Detection Directly from Biological Samples.

Hongmei Cao, Xin Zhou, Yong Zeng

Abstract read
In one paragraph

Article in Sensors and actuators. B, Chemical, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Review
  3. Anion recognition properties of acridine-urea conjugate in bulk and silica nanopore systems.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Article
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  5. Article
  6. Review
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  8. Review
  9. Article
  10. Review
  11. Ultrafast Detection of Exosomal RNAsACS applied nano materials · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. Mitochondrial isolation: when size matters.Wellcome open research · 2020
    Review
  16. Review
  17. Review
  18. Review
  19. Article
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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

3 authors at 2 institutions in 1 country.

Hongmei CaoDepartment of Chemistry, University of Kansas, Lawrence, KS 66045.
Xin ZhouDepartment of Chemistry, University of Kansas, Lawrence, KS 66045.
Yong ZengDepartment of Chemistry, University of Kansas, Lawrence, KS 66045.
University of Kansas · USThe University of Kansas Cancer Center · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
Understanding the mechanobiology of stem cells in a microengineered 3D cardiac tissue environment with cardiomyopathyP20GM103638 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI HOLMSTROM, ERIK D · 2012 to 2021
$22.1M
Integrated exosomes profiling for minimally invasive diagnosis and monitoring of cancerR33CA214333 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI GODWIN, ANDREW K., SAMUEL, GLENSON · 2017 to 2019
$1.2M
Integrated Microfluidic Exosome Profiling for Early Detection of CancerR21CA186846 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI ZENG, YONG · 2014 to 2016
$645k
Integrated Digital Microfluidic Platforms for Next-Generation GlycomicsR21CA207816 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI ZENG, YONG · 2016 to 2017
$585k
Microfluidic Integrative Circulating miRNA Profiling for Cancer DiagnosisR21EB024101 · NIBIB · UNIVERSITY OF KANSAS LAWRENCE · PI DOYLE, PATRICK S, ZENG, YONG · 2017 to 2018
$411k
NCI NIH HHS R21 CA186846NCI NIH HHS R21 CA207816NCI NIH HHS R33 CA214333NIBIB NIH HHS R21 EB024101NIGMS NIH HHS P20 GM103418NIGMS NIH HHS P20 GM103638
6 · The paper itself

Abstract

There is an urgent need of sensitive bioanalytical platforms for sensitive and precise quantification of low-abundance microRNA targets in complex biological samples, including liquid biopsies of tumors. Many of current miRNA biosensing methods require laborious sample pretreatment procedures, including extraction of total RNA, which largely limits their biomedical and clinical applications. Herein we developed an integrated Microfluidic Exponential Rolling Circle Amplification (MERCA) platform for sensitive and specific detection of microRNAs directly in minimally processed samples. The MERCA system integrates and streamlines solid-phase miRNA isolation, miRNA-adapter ligation, and a dualphase exponential rolling circle amplification (eRCA) assay in one analytical workflow. By marrying the advantages of microfluidics in leveraging bioassay performance with the high sensitivity of eRCA, our method affords a remarkably low limit of detection at <10 zeptomole levels, with the ability to discriminate single-nucleotide difference. Using the MERCA chip, we demonstrated quantitative detection of miRNAs in total RNA, raw cell lysate, and cellderived exosomes. Comparing with the parallel TaqMan RT-qPCR measurements verified the adaptability of the MERCA system for detection of miRNA biomarkers in complex biological materials. In particular, high sensitivity of our method enables direct detection of low-level exosomal miRNAs in as few as 2 × 10

Indexed as

cell-derived exosomescomplex biological samplesMicrofluidic Exponential Rolling Circle Amplification (MERCA)microRNA detectionraw cell lysate

Identifiers

PMID30533973
PMCPMC6284813
OpenAlexW2895587884

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.