Evidence map›Paper›PMID 20116881›Full record

ArticleLung cancer (Amsterdam, Netherlands)2010

Cystic fibrosis transmembrane conductance regulator gene mutation and lung cancer risk.

Yafei Li, Zhifu Sun, Yanhong Wu, Dusica Babovic-Vuksanovic, Yan Li, Julie M Cunningham, Vernon S Pankratz, Ping Yang

Open access · greenAbstract read
In one paragraph

Article in Lung cancer (Amsterdam, Netherlands), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Ion Channels in Lung Cancer.Reviews of physiology, biochemistry and pharmacology · 2021
    Review
  6. Review
  7. Cystic Fibrosis, CFTR, and Colorectal Cancer.International journal of molecular sciences · 2020
    Review
  8. Article
  9. Article
  10. Role of ion channels in gastrointestinal cancer.World journal of gastroenterology · 2019
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Lower Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Promotes the Proliferation and Migration of Endometrial Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Yafei LiDepartment of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Zhifu Sun
Yanhong Wu
Dusica Babovic-Vuksanovic
Yan Li
Julie M Cunningham
Vernon S Pankratz
Ping Yang
Mayo Clinic · US

Funding

ALPHA 1 AD CARRIERS AND LUNG CANCER RISKR01CA080127 · NCI · MAYO CLINIC ROCHESTER · PI YANG, PING · 2000 to 2009
$4.4M
Genetic Determinants of Lung Cancer SurvivalR01CA084354 · NCI · MAYO CLINIC ROCHESTER · PI YANG, PING · 2001 to 2012
$4.0M
DEVELOPMENT OF LUNG CANCER EPIDEMIOLOGY RESEARCHR03CA077118 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI YANG, PING · 1997 to 1998
–
NCI NIH HHS CA 77118NCI NIH HHS CA 80127NCI NIH HHS CA 84354NCI NIH HHS R01 CA080127NCI NIH HHS R01 CA084354NCI NIH HHS R03 CA077118
6 · The paper itself

Abstract

The cystic fibrosis transmembrane conductance regulator (CFTR) holds an important role in retaining lung function, but its association with lung cancer is unclear. A case-control study was conducted to determine the possible associations of the genetic variants in the CFTR gene with lung cancer risk. Genotypes of the most common deletion DeltaF508, one functional SNP, and eight tag SNPs in the CFTR gene were determined in 574 lung cancer patients and 679 controls. A logistic regression model, adjusting for known risk factors, was used to evaluate the association of each variant with lung cancer risk, as confirmation haplotype and sub-haplotype analyses were performed. DeltaF508 deletion and genotypes with minor alleles in one tag SNP, rs10487372, and one functional SNP, rs213950, were inversely associated with lung cancer risk. The results of haplotype and sub-haplotype analyses were consistent with single variant analysis, all pointing to deletion DeltaF508 being the key variant for significant haplotypes and sub-haplotypes. Individuals with 'deletion-T' (DeltaF508/rs10487372) haplotype had a 68% reduced risk for lung cancer compared to common haplotype 'no-deletion-C' (OR=0.32; 95% CI=0.15-0.68; p=0.01). Genetic variations in the CFTR gene might modulate the risk of lung cancer. This study, for the first time, provides evidence of a protective role of the CFTR deletion carrier in the etiology of lung cancer.

Indexed as

AgedAged, 80 and overAllelesCase-Control StudiesCystic Fibrosis Transmembrane Conductance RegulatorFemaleGene DeletionGenetic Predisposition to DiseaseHaplotypesHumansLung NeoplasmsMaleMiddle AgedPolymorphism, Single NucleotideCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID20116881
PMCPMC2895007
OpenAlexW2169451213

What OpenQuestion holds

Textmetadata
LicenceTDM
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.