Evidence map›Paper›PMID 37552462›Full record

ArticleAnalytical sciences : the international journal of the Japan Society for Analytical Chemistry2023

Trigger-activated autonomous DNA machine for amplified liver cancer biomarker microRNA21 imaging.

Jiqin Su, Maolin Wang, Peiyi Lin, Zhishu Huang, Guibin Li, Xiangru Chen, Huidi Yan, Lixin Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Electrochemical analysis of miRNA for liquid biopsy.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2026
    Article
  2. Article
  3. Review
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

8 authors at 1 institution in 1 country.

Jiqin SuThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China.
Maolin WangThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China.
Peiyi LinThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China.
Zhishu HuangThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China.
Guibin LiThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China.
Xiangru ChenThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China.
Huidi YanThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China. yhd351252@163.com.
Lixin ZhouThe Second Affiliated Hospital of Xiamen Medical College, Xiamen, 361021, Fujian, China. zhoulix318@163.com.
The Second Affiliated Hospital of Xiamen Medical College

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA-21 (miRNA-21) is a kind of RNA that exists in biological fluids such as blood, urine and saliva. It has over expression in liver cancer and has different expression in different stages of cancer. However, due to the characteristics of small base number, short length, low abundance and easy degradation of miRNA-21, the detection of miRNA-21 is a challenging subject. Visualization, sensitive, specific and stable detection of tumor suppressor or oncogene microRNAs (miRNAs) remains challenging and is highly significant for clinical diagnostics. To solve this problem, we have developed a target-triggered hybridization assembly DNA machine for intracellular miRNA imaging based on strand displacement amplification (SDA) and branched hybridization chain reaction (B-HCR). In this approach, the target miRNA could hybridize with the template probe to trigger the SDA, resulting in the formation of nicked fragments (NFs) that hybridized with hairpin probe1 (HP1). The opened HP1 could hybridize with hairpin probe2 (HP2), leading to the self-assembly of hyperbranched DNA nanostructures through B-HCR. As expected, the newly developed method exhibits a detection limit down to 11.3 pM miRNA-21 and achieves high selectivity toward miRNA-21 against other interfering miRNAs. Due to its superior sensitivity and selectivity, our method can be further used to detect miRNA-21 in human serum samples. By taking advantage of intelligent design, the proposed method was also used for image miRNA-21 expression levels in different cell lines. This method shows a broad application in clinical diagnosis.

Indexed as

Biosensing TechniquesLiver NeoplasmsMicroRNAsBiomarkers, TumorChromosomal Proteins, Non-HistoneDNAHumansLimit of DetectionNucleic Acid Amplification TechniquesBiomarkers, TumorChromosomal Proteins, Non-HistoneDNAMicroRNAsMIRN21 microRNA, humanBranched hybridization chain reaction (B-HCR)ImagingmiRNAStrand-displacement amplification (SDA)

Identifiers

PMID37552462
OpenAlexW4385664844

What OpenQuestion holds

Textmetadata
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.