Evidence map›Paper›PMID 40626205›Full record

ReviewSmart molecules : open access2023

Smart DNA sensors-based molecular identification for cancer subtyping.

Yingying Gao, Mengyi Xiong, Chaonan Gong, Bo Wang, Longwei Bai, Xiao-Bing Zhang

Abstract readReview
In one paragraph

Review in Smart molecules : open access, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  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

6 authors.

Yingying GaoMolecular Science and Biomedicine Laboratory State Key Laboratory of Chemo/Biosensing and Chemometrics Collaborative Innovation Center for Chemistry and Molecular Medicine College of Chemistry and Chemical Engineering Hunan University Changsha Hunan China.
Mengyi XiongMolecular Science and Biomedicine Laboratory State Key Laboratory of Chemo/Biosensing and Chemometrics Collaborative Innovation Center for Chemistry and Molecular Medicine College of Chemistry and Chemical Engineering Hunan University Changsha Hunan China.
Chaonan GongMolecular Science and Biomedicine Laboratory State Key Laboratory of Chemo/Biosensing and Chemometrics Collaborative Innovation Center for Chemistry and Molecular Medicine College of Chemistry and Chemical Engineering Hunan University Changsha Hunan China.
Bo WangMolecular Science and Biomedicine Laboratory State Key Laboratory of Chemo/Biosensing and Chemometrics Collaborative Innovation Center for Chemistry and Molecular Medicine College of Chemistry and Chemical Engineering Hunan University Changsha Hunan China.
Longwei BaiMolecular Science and Biomedicine Laboratory State Key Laboratory of Chemo/Biosensing and Chemometrics Collaborative Innovation Center for Chemistry and Molecular Medicine College of Chemistry and Chemical Engineering Hunan University Changsha Hunan China.
Xiao-Bing ZhangMolecular Science and Biomedicine Laboratory State Key Laboratory of Chemo/Biosensing and Chemometrics Collaborative Innovation Center for Chemistry and Molecular Medicine College of Chemistry and Chemical Engineering Hunan University Changsha Hunan China.ORCID https://orcid.org/0000-0002-4010-0028

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular subtyping of cancer can greatly help to understand the development of disease and predict tumor behavior. Exploring detection methods for precise subtyping is appealing to prognosis and personalized therapy. During the past decades, DNA-based biosensors have exhibited great potential in cancer diagnosis due to their structural programmability and functional diversity. Despite the encouraging progress that has been made, there remains an issue in improving the accuracy and sensitivity of cancer subtyping due to the complex process of disease, especially in preclinical or clinical applications. To accelerate the development of DNA sensors in the identification of cancer subtypes, in this review, we summarized their advances in molecular subtyping by analyzing the heterogeneity in categories and levels of biomarkers between cancer subtypes. The strategies toward genomic and proteomic heterogeneity in cells or on the cell surface, as well as the cancer excretions including extracellular vesicles (EVs) and microRNA (miRNAs) in serum, are summarized. Current challenges and the opportunities of DNA-based sensors in this field are also discussed.

Indexed as

biomarkersDNA sensorslogical computingmolecular subtyping

Identifiers

PMID40626205
PMCPMC12118291

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.