Evidence map›Paper›PMID 36207395›Full record

ArticleCommunications biology2022

Rapid quantification of miRNAs using dynamic FRET-FISH.

Juyoung Kim, Chanshin Kang, Soochul Shin, Sungchul Hohng

Abstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
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  3. Review
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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

4 authors.

Juyoung KimDepartment of Physics and Astronomy, and Institute of Applied Physics, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0002-6317-1988
Chanshin KangDepartment of Physics and Astronomy, and Institute of Applied Physics, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0002-2108-1730
Soochul ShinDepartment of Physics and Astronomy, and Institute of Applied Physics, Seoul National University, Seoul, Republic of Korea. tlstncjf@snu.ac.kr.
Sungchul HohngDepartment of Physics and Astronomy, and Institute of Applied Physics, Seoul National University, Seoul, Republic of Korea. shohng@snu.ac.kr.ORCID 0000-0002-7131-2138

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are short regulatory RNAs that control gene expression at the post-transcriptional level. Various miRNAs playing important roles in cancer development are emerging as promising diagnostic biomarkers for early cancer detection. Accurate miRNA detection, however, remains challenging because they are small and highly homologous. Recently developed miRNA detection techniques based on single-molecule imaging enabled highly specific miRNA quantification without amplification, but the time required for these techniques to detect a single miRNA was larger than 10 minutes, making rapid profiling of numerous miRNAs impractical. Here we report a rapid miRNA detection technique, dynamic FRET-FISH, in which single-molecule imaging at high probe concentrations and thus high-speed miRNA detection is possible. Dynamic FRET-FISH can detect miRNAs in 10 s at 1.2 μM probe concentration while maintaining the high-specificity of single-nucleotide discrimination. We expect dynamic FRET-FISH will be utilized for early detection of cancers by profiling hundreds of cancer biomarkers in an hour.

Indexed as

MicroRNAsBiomarkers, TumorFluorescence Resonance Energy TransferNucleotidesBiomarkers, TumorMicroRNAsNucleotides

Identifiers

PMID36207395
PMCPMC9546913

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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.