Evidence map›Paper›PMID 21792076›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2011

Systematic evaluation of genetic variants in three biological pathways on patient survival in low-stage non-small cell lung cancer.

V Shane Pankratz, Zhifu Sun, Jeremiah Aakre, Yan Li, Cassandra Johnson, Yolanda I Garces, Marie C Aubry, Julian R Molina, Dennis A Wigle, Ping Yang

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Genetic variations and patient-reported quality of life among patients with lung cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2012
    Article
  12. Article
  13. Review
  14. 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

10 authors at 3 institutions in 2 countries.

V Shane PankratzDivision of Biomedical Statistics and Informatics, Jinling Hospital, Nanjing University, School of Medicine, Nanjing, People's Republic of China.
Zhifu Sun
Jeremiah Aakre
Yan Li
Cassandra Johnson
Yolanda I Garces
Marie C Aubry
Julian R Molina
Dennis A Wigle
Ping Yang
Mayo Clinic · USNanjing University · CNNanjing General Hospital of Nanjing Military Command · CN

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 R01 CA080127NCI NIH HHS R01 CA084354NCI NIH HHS R01 CA80127NCI NIH HHS R01 CA84354NCI NIH HHS R03 CA077118NCI NIH HHS R03 CA77118
6 · The paper itself

Abstract

introductionStudies from selected candidate genes suggest that single-nucleotide polymorphisms (SNPs) involved in glutathione metabolism, DNA repair, or inflammatory responses may affect overall survival (OS) in stages I to II or low-stage non-small cell lung cancer (LS-NSCLC); however, results are inconclusive. In this study, we took a systematic pathway-based approach to simultaneously evaluate the impact of genetic variation from these three pathways on OS after LS-NSCLC diagnosis.

methodsDNA from 647 patients with LS-NSCLC was genotyped for 480 SNPs (tag-SNPs) tagging 57 genes from the three candidate pathways. Associations of tag-SNPs with OS were assessed at the individual SNP and whole gene levels, adjusting for age, tumor stage, surgery type, and adjuvant therapy. The genotype combinations of the SNPs associated with OS were also estimated.

resultsAmong the 412 tag-SNPs that were successfully genotyped and passed quality assessments, 28 showed association with OS (p < 0.05). Two of the 28 were estimated to have less than a 20% chance of being false positives (rs3768490 in GSTM5: p = 1.32 × 10, q = 0.06; rs1729786 in ABCC4: p = 9.25 × 10, q = 0.20). Gene-based analysis suggested that in addition to GSTM5 and ABCC4, variation in two other genes, PTGS2 and GSTA2, was also associated with OS.

conclusionsWe describe further evidence that variations in genes involved in the glutathione and inflammatory response pathways are associated with OS in patients with LS-NSCLC. Further studies are warranted to verify our findings and elucidate their functional mechanisms and clinical utility leading to improved survival for patients with lung cancer.

Indexed as

AdenocarcinomaAgedATP-Binding Cassette, Sub-Family C ProteinsBiomarkers, TumorCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellCyclooxygenase 2DNA, NeoplasmDNA RepairFemaleFollow-Up StudiesGenotypeGlutathioneGlutathione TransferaseHumansIsoenzymesABCC4 protein, humanATP-Binding Cassette, Sub-Family C ProteinsBiomarkers, TumorCyclooxygenase 2DNA, NeoplasmGlutathioneglutathione S-transferase alphaGlutathione TransferaseGSTM5 protein, humanIsoenzymesPTGS2 protein, human

Identifiers

PMID21792076
PMCPMC3158278
OpenAlexW2093467686

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.