Evidence map›Paper›PMID 26678430›Full record

ArticleScientific reports2015

A Fluorescent Tile DNA Diagnocode System for In Situ Rapid and Selective Diagnosis of Cytosolic RNA Cancer Markers.

Kyung Soo Park, Seung Won Shin, Min Su Jang, Woojung Shin, Kisuk Yang, Junhong Min, Seung-Woo Cho, Byung-Keun Oh, Jong Wook Bae, Sunghwan Jung and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Challenges and Perspectives of DNA Nanostructures in Biomedicine.Angewandte Chemie (International ed. in English) · 2020
    Review
  3. Review
  4. Article
  5. Article
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

12 authors at 5 institutions in 2 countries.

Kyung Soo ParkSchool of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, 440-746, South Korea.
Seung Won ShinSchool of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, 440-746, South Korea.
Min Su JangSchool of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, 440-746, South Korea.
Woojung ShinSchool of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, 440-746, South Korea.
Kisuk YangDepartment of Biotechnology, Yonsei University, Seoul, 120-749, South Korea.
Junhong MinSchool of Integrative Engineering, Chung-Ang University, Seoul, 156-756, South Korea.
Seung-Woo ChoDepartment of Biotechnology, Yonsei University, Seoul, 120-749, South Korea.
Byung-Keun OhDepartment of Chemical and Biomolecular Engineering, Sogang University, Seoul, 121-742, South Korea.
Jong Wook BaeSchool of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, 440-746, South Korea.
Sunghwan JungDepartment of Engineering Science and Mechanics, Virginia Tech, Blacksburg, VA 24061, USA.
Jeong-Woo ChoiDepartment of Chemical and Biomolecular Engineering, Sogang University, Seoul, 121-742, South Korea.
Soong Ho UmSchool of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, 440-746, South Korea.
Sungkyunkwan University · KRSogang University · KRYonsei University · KRChung-Ang University · KRVirginia Tech · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate cancer diagnosis often requires extraction and purification of genetic materials from cells, and sophisticated instrumentations that follow. Otherwise in order to directly treat the diagnostic materials to cells, multiple steps to optimize dose concentration and treatment time are necessary due to diversity in cellular behaviors. These processes may offer high precision but hinder fast analysis of cancer, especially in clinical situations that need rapid detection and characterization of cancer. Here we present a novel fluorescent tile DNA nanostructure delivered to cancer cytosol by employing nanoparticle technology. Its structural anisotropicity offers easy manipulation for multifunctionalities, enabling the novel DNA nanostructure to detect intracellular cancer RNA markers with high specificity within 30 minutes post treatment, while the nanoparticle property bypasses the requirement of treatment optimization, effectively reducing the complexity of applying the system for cancer diagnosis. Altogether, the system offers a precise and rapid detection of cancer, suggesting the future use in the clinical fields.

Indexed as

Biomarkers, TumorCytosolDNAFluorescence Resonance Energy TransferFluorescent DyesHumansMicroscopy, Electron, TransmissionNanostructuresNeoplasmsOligonucleotide Array Sequence AnalysisRNABiomarkers, TumorDNAFluorescent DyesRNA

Identifiers

PMID26678430
PMCPMC4683441
OpenAlexW2323619243

What OpenQuestion holds

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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.