Evidence map›Paper›PMID 30303958›Full record

ArticlePloS one2018

Novel RNA aptamers targeting gastrointestinal cancer biomarkers CEA, CA50 and CA72-4 with superior affinity and specificity.

Qing Pan, Carmen O K Law, Mingo M H Yung, K C Han, Yuen Lam Pon, Terrence Chi Kong Lau

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. 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 at 1 institution in 1 country.

Qing PanDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China.
Carmen O K LawDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China.
Mingo M H YungDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China.
K C HanDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China.
Yuen Lam PonDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China.
Terrence Chi Kong LauDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China.ORCID 0000-0002-7505-7306
City University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer is the third most common cause of death from cancer in the world and it remains difficult to cure in Western countries, primarily because most patients present with advanced disease. Currently, CEA, CA50 and CA72-4 are commonly used as tumor markers for gastric cancer by immunoassays. However, the drawback and conundrum of immunoassay are the unceasing problem in standardization of quality of antibodies and time/effort for the intensive production. Therefore, there is an urgent need for the development of a standardized assay to detect gastric cancer at the early stage. Aptamers are DNA or RNA oligonucleotides with structural domain which recognize ligands such as proteins with superior affinity and specificity when compared to antibodies. In this study, SELEX (Systematic Evolution of Ligands by Exponential enrichment) technique was adopted to screen a random 30mer RNA library for aptamers targeting CEA, CA50 and CA72-4 respectively. Combined with high-throughput sequencing, we identified 6 aptamers which specifically target for these three biomarkers of gastrointestinal cancer. Intriguingly, the predicted secondary structures of RNA aptamers from each antigen showed significant structural similarity, suggesting the structural recognition between the aptamers and the antigens. Moreover, we determined the dissociation constants of all the aptamers to their corresponding antigens by fluorescence spectroscopy, which further demonstrated high affinities between the aptamers and the antigens. In addition, immunostaining of gastric adenocarcinoma cell line AGS using CEA Aptamer probe showed positive fluorescent signal which proves the potential of the aptamer as a detection tool for gastric cancer. Furthermore, substantially decreased cell viability and growth were observed when human colorectal cell line LS-174T was transfected with each individual aptamers. Taking together, these novel RNA aptamers targeting gastrointestinal cancer biomarker CEA, CA50 and CA72-4 will aid further development and standardization of clinical diagnostic method with better sensitivity and specificity, and potentially future therapeutics development of gastric cancer.

Indexed as

AdenocarcinomaAntigens, Tumor-Associated, CarbohydrateAptamers, NucleotideBiomarkers, TumorCarcinoembryonic AntigenCell Line, TumorCell SurvivalDNAGastrointestinal NeoplasmsGene LibraryHeLa CellsHumansPrognosisRNA, NeoplasmSELEX Aptamer TechniqueSensitivity and SpecificityAntigens, Tumor-Associated, CarbohydrateAptamers, NucleotideBiomarkers, TumorCA-50 antigenCA-72-4 antigenCarcinoembryonic AntigenDNARNA, Neoplasm

Identifiers

PMID30303958
PMCPMC6179186
OpenAlexW2950630417

What OpenQuestion holds

Textmetadata
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.