Evidence map›Paper›PMID 33212417›Full record

ArticleTranslational oncology2021

Diagnostic value of quantification of circulating free DNA for gall bladder cancer using a chemiluminescence DNA biosensor system based on DNA G-quadruplex/ hemin enzyme.

Hua Ying, Sun Fengying, Hu Feng, Wu Yanhong, Xia Xianru, Tang Xiaolei

Open access · goldAbstract read
In one paragraph

Article in Translational oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. The footprint of gut microbiota in gallbladder cancer: a mechanistic review.Frontiers in cellular and infection microbiology · 2024
    Review
  6. Molecular Diagnosis and Cancer Prognosis-A Concise Review.Diagnostics (Basel, Switzerland) · 2023
    Review
  7. Review
  8. Article
  9. 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

6 authors at 3 institutions in 1 country.

Hua YingVascular disease research center, Basic Medical Laboratory, the Second affiliated Hospital of Wannan Medical College, Kangfu Road 10# of Jinghu District, Wuhu 241000, China; School of Nursing, Wannan Medical College, Wuhu 241000, China.
Sun FengyingDepartment of Clinical Laboratory, The second people's hospital of Wuhu city, Wuhu 241000, China.
Hu FengDepartment of blood transfusion, Yijishan Hospital of Wannan Medical College, Wuhu 241000, China.
Wu YanhongDepartment of immunology and microbiology, Wannan Medical College, Wuhu 241000, China.
Xia XianruDepartment of Clinical Laboratory, Affiliated Taihe hospital of Hubei Univiersity of Medicine, Renminnan Road 32# of Maojian District, Shiyan 442008, China.
Tang XiaoleiVascular disease research center, Basic Medical Laboratory, the Second affiliated Hospital of Wannan Medical College, Kangfu Road 10# of Jinghu District, Wuhu 241000, China. Electronic address: 278471655@qq.com.
Wannan Medical College · CNTaihe Hospital · CNWuhu Fourth People Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gall bladder cancer (GBC) is an insidious but rapidly progressed disease with a poor prognosis and high mortality rate. To explore a novel method for GBC diagnosis, we quantified circulating free DNA (cfDNA) in serum samples from 228 participants, including 83 patients with GBC, 75 patients with cholecystitis, and 70 healthy donors, using a chemiluminescence DNA biosensor system based on DNA G-quadruplex/hemin enzyme. We measured β-actin gene expression to evaluate serum cfDNA levels representing as chemiluminescence intensity with the addition of sufficient probes. We analyzed associations of cfDNA quantities in serum samples and corresponding pathological stages and found that the concentration of cfDNA was significantly higher in GBC group than in the healthy control and cholecystitis groups. The levels of cfDNA were significantly associated with TNM stage, lymph node involvement, metastasis, and jaundice. The ROC curves showed that the diagnostic value of chemiluminescence DNA biosensor system was nearly equivalent to that of qPCR. Our method can distinguish patients with GBC from healthy donors and patients with cholecystitis clearly; however, this method was not available to distinguish patients with cholecystitis from the healthy controls. In summary, cfDNA maybe serve as a new diagnostic and noninvasive marker for the diagnosis of GBC using chemiluminescence DNA biosensor system based on DNA G-quadruplex/hemin enzyme.

Indexed as

Chemiluminescence dna biosensorCirculating free dna (CFDNA)DiagnosisDNA G-quadruplex/hemin enzymeGall bladder carcinoma (GBC)

Identifiers

PMID33212417
PMCPMC7679247
OpenAlexW3104922845

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.