Evidence map›Paper›PMID 38492362›Full record

ArticleBiosensors & bioelectronics2024

Label-free plasmonic spectral profiling of serum DNA.

Peng Zheng, Piyush Raj, Le Liang, Lintong Wu, Santosh Kumar Paidi, Jeong Hee Kim, Ishan Barman

Abstract read
In one paragraph

Article in Biosensors & bioelectronics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Plasmonic Gold Prism Array for Digital Surface-Enhanced Raman Spectroscopy Sensing.The journal of physical chemistry. C, Nanomaterials and interfaces · 2024
    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

7 authors.

Peng ZhengDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, United States.
Piyush RajDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, United States.
Le LiangDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, United States; The Institute for Advanced Studies, Wuhan University, Wuhan, 430072, China; Department of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, 430071, China.
Lintong WuDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, United States.
Santosh Kumar PaidiDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, United States.
Jeong Hee KimDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, United States.
Ishan BarmanDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, United States; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, United States; The Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, United States. Electronic address: ibarman@jhu.edu.

Funding

Next-generation optical nanoprobes: From quantum biosensing to cellular monitoringR35GM149272 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ISHAN BARMAN · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM149272
6 · The paper itself

Abstract

Genetic and epigenetic modifications are linked to the activation of oncogenes and inactivation of tumor suppressor genes. Likewise, the associated molecular alternations can best inform precision medicine for personalized tumor treatment. Therefore, performing characterization of genetic and epigenetic alternations at the molecular level represents a crucial step in early diagnosis and/or therapeutics of cancer. However, the prevailing methods for DNA analysis involve a series of tedious and complicated steps, in which important genetic and epigenetic information could be lost or altered. To provide a potential approach for non-invasive, direct, and efficient DNA analysis, herein, we present a promising strategy for label-free molecular profiling of serum DNA in its pristine form by fusing surface-enhanced Raman spectroscopy with machine learning on a superior plasmonic nanostructured platform. Using DNA methylation and single-point mutation as two case studies, the presented strategy allows a well-balanced sensitive and specific detection of epigenetic and genetic changes at the single-nucleotide level in serum. We envision the presented label-free strategy could serve as a versatile tool for direct molecular profiling in pristine forms of a wide range of biological markers and aid biomedical diagnostics as well as therapeutics.

Indexed as

Biosensing TechniquesMetal NanoparticlesNeoplasmsDNADNA MethylationEpigenesis, GeneticHumansSpectrum Analysis, RamanDNADNAMachine learningMethylationSERSSingle-point mutation

Identifiers

PMID38492362
PMCPMC11056035

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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.