Evidence map›Paper›PMID 24349364›Full record

ArticlePloS one2013

Impacts of CA9 gene polymorphisms on urothelial cell carcinoma susceptibility and clinicopathologic characteristics in Taiwan.

Shian-Shiang Wang, Yu-Fan Liu, Yen-Chuan Ou, Chuan-Shu Chen, Jian-Ri Li, Shun-Fa Yang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. The impacts ofJournal of Cancer · 2023
    Article
  3. Gene expression of carbonic anhydrase 9 (CA9) inJournal of medicine and life · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Effect ofInternational journal of medical sciences · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Impacts of ICAM-1 gene polymorphisms on urothelial cell carcinoma susceptibility and clinicopathologic characteristics in Taiwan.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    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.

Shian-Shiang WangInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan ; Division of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
Yu-Fan LiuDepartment of Biomedical Sciences, Chung Shan Medical University, Taichung, Taiwan.
Yen-Chuan OuDivision of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
Chuan-Shu ChenDivision of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
Jian-Ri LiDivision of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
Shun-Fa YangInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan ; Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.
Taichung Veterans General Hospital · TWChung Shan Medical University · TWChung Shan Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarbonic anhydrase 9 (CA9) is reportedly overexpressed in several types of carcinomas and is generally considered a marker of malignancy. The current study explored the effect of CA9 gene polymorphisms on the susceptibility of developing urothelial cell carcinoma (UCC) and the clinicopathological status. METHODOLOGY AND PRINCIPAL

findingsA total of 442 participants, including 221 healthy people and 221 patients with UCC, were recruited for this study. Four single-nucleotide polymorphisms (SNPs) of the CA9 gene were assessed by a real-time PCR with the TaqMan assay. After adjusting for other co-variants, the individuals carrying at least one A allele at CA9 rs1048638 had a 2.303-fold risk of developing UCC than did wild-type (CC) carriers. Furthermore, UCC patients who carried at least one A allele at rs1048638 had a higher invasive stage risk (p< 0.05) than did patients carrying the wild-type allele. Moreover, among the UCC patients with smoker, people with at least one A allele of CA9 polymorphisms (rs1048638) had a 4.75-fold (95% CI = 1.204-18.746) increased risk of invasive cancer.

conclusionThe rs1048638 polymorphic genotypes of CA9 might contribute to the prediction of susceptibility to and pathological development of UCC. This is the first study to provide insight into risk factors associated with CA9 variants in carcinogenesis of UCC in Taiwan.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticAgedAged, 80 and overAllelesAntigens, NeoplasmCarbonic Anhydrase IXCarbonic AnhydrasesCarcinomaCase-Control StudiesFemaleGene FrequencyGenotypeHumansMaleMiddle AgedAntigens, NeoplasmCA9 protein, humanCarbonic Anhydrase IXCarbonic Anhydrases

Identifiers

PMID24349364
PMCPMC3862582
OpenAlexW2029679939

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.