Evidence map›Paper›PMID 35520768›Full record

ArticleRSC advances2019

The label-free detection and distinction of CYP2C9-expressing and non-expressing cells by surface-enhanced Raman scattering substrates based on bimetallic AuNPs-AgNWs.

Xiaowei Cao, Shuai Chen, Zhenyu Wang, Yong Liu, Xiaowei Luan, Sicong Hou, Wei Li, Hongcan Shi

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 18% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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 3 institutions in 1 country.

Xiaowei CaoInstitute of Translational Medicine, Medical College, Yangzhou University Yangzhou 225001 PR China weili@yzu.edu.cn shihongcan@yzu.edu.cn.ORCID https://orcid.org/0000-0003-1845-9111
Shuai ChenInstitute of Translational Medicine, Medical College, Yangzhou University Yangzhou 225001 PR China weili@yzu.edu.cn shihongcan@yzu.edu.cn.
Zhenyu WangInstitute of Translational Medicine, Medical College, Yangzhou University Yangzhou 225001 PR China weili@yzu.edu.cn shihongcan@yzu.edu.cn.
Yong LiuSchool of Life Science and Medicine, Dalian University of Technology Panjin 124221 China.
Xiaowei LuanSchool of Life Science and Medicine, Dalian University of Technology Panjin 124221 China.
Sicong HouInstitute of Translational Medicine, Medical College, Yangzhou University Yangzhou 225001 PR China weili@yzu.edu.cn shihongcan@yzu.edu.cn.
Wei LiInstitute of Translational Medicine, Medical College, Yangzhou University Yangzhou 225001 PR China weili@yzu.edu.cn shihongcan@yzu.edu.cn.
Hongcan ShiInstitute of Translational Medicine, Medical College, Yangzhou University Yangzhou 225001 PR China weili@yzu.edu.cn shihongcan@yzu.edu.cn.
Yangzhou University · CNDalian University of Technology · CNState Administration of Traditional Chinese Medicine of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytochrome P450 2C9 (CYP2C9) is capable of catalyzing the biotransformation of endogenous compounds in cells, indicating that this enzyme could change the intracellular environment and is related to the pathogenesis of diseases. Currently, it is still a challenge to study the differences in cellular components between CYP2C9-expressing and non-expressing cells. In this study, employing a Au nanoparticles-Ag nanowires (AuNPs-AgNWs) decorated silicon wafer as a novel non-destructive and label-free tool, we applied surface-enhanced Raman scattering (SERS) spectroscopy to detect and distinguish the cellular composition of CYP2C9-expressing cells (293T-Mig-2C9) and non-expressing cells (293T-Mig-R1). AgNWs with high surface roughness were formed by modification of AuNPs onto their surface by electrostatic interactions, which enabled them to exhibit greatly enhanced SERS ability. Then, they were employed to fabricate SERS substrates

Identifiers

PMID35520768
PMCPMC9063916
OpenAlexW2943731610

What OpenQuestion holds

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LicenceCC BY
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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.