Evidence map›Paper›PMID 32594259›Full record

ArticleMikrochimica acta2020

Functionalized reduced graphene oxide with aptamer macroarray for cancer cell capture and fluorescence detection.

Wenhui Qian, Zhaoyi Miao, Xiao-Jing Zhang, Xiao-Tong Yang, Ying-Ying Tang, Yu Ying Tang, Lin Yu Hu, Su Li, Dong Zhu, Haibo Cheng

Abstract read
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In one paragraph

Article in Mikrochimica acta, 2020. 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
–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. Review
  2. Review
  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

10 authors.

Wenhui QianSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Zhaoyi MiaoSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Xiao-Jing ZhangSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Xiao-Tong YangSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Ying-Ying TangSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Yu Ying TangSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Lin Yu HuSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Su LiSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China.
Dong ZhuSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, People's Republic of China. dongzhu@njucm.edu.cn.
Haibo ChengJiangsu Collaborative Innovation Center of Traditional Chinese Medicine Prevention and Treatment of Tumor, the First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210023, China. hbcheng@njucm.edu.cn.

Funding

National Natural Science Foundation of China 81573388National Natural Science Foundation of China 81573910National Natural Science Foundation of China 81930117
6 · The paper itself

Abstract

An integrated aptamer macroarray functionalized with reduced graphene oxide (rGO) to specifically capture and sensitively detect cancer cells is reported. The capture for cancer cells is based on effective recognition of the modified rGO surface through the aptamer against epithelial cell adhesion molecule (EpCAM). The rough structure of rGO enhances morphologic interactions between rGO film interface and the cancer cells, while super-hydrophilicity of modified rGO hinders nonspecific cell capture. The synergistic interactions offer the aptamer macroarray high efficiency of cancer cell capture. By means of a turn-on fluorescence strategy based on the conformation change of the aptamer induced by the target recognition, the enriched cancer cells can be directly read out at excitation/emission wavelengths of 550/680 nm without washing, separation, and dying steps. The working range is 1 × 10

Indexed as

Neoplastic Cells, CirculatingAptamers, NucleotideBase SequenceCell Line, TumorCell SeparationEpithelial Cell Adhesion MoleculeFluorescenceFluorescence Resonance Energy TransferGraphiteHumansHuman Umbilical Vein Endothelial CellsImmobilized Nucleic AcidsLimit of DetectionPyrenesAptamers, NucleotideEPCAM protein, humanEpithelial Cell Adhesion Moleculegraphene oxideGraphiteImmobilized Nucleic AcidsPyrenesAptamer macroarrayReduced graphene oxide filmSensitively detect cancer cellsSpecifically capture cancer cells

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.