Evidence map›Paper›PMID 25716425›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2015

A genetic variation in microRNA target site of KRT81 gene is associated with survival in early-stage non-small-cell lung cancer.

S Y Lee, J E Choi, H S Jeon, M J Hong, Y Y Choi, H G Kang, S S Yoo, E B Lee, J Y Jeong, W K Lee and 7 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2015. 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
1.5field-weighted citation impact, top 19% 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, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. MicroRNAs in Genetic Etiology of Human Diseases.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. KRT81 miR-SNP rs3660 is associated with risk and survival of NSCLC.Annals of oncology : official journal of the European Society for Medical Oncology · 2016
    Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

S Y LeeLung Cancer Center, Kyungpook National University Medical Center, Daegu; Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu.
J E ChoiLung Cancer Center, Kyungpook National University Medical Center, Daegu; Department of Biochemistry and Cell Biology, School of Medicine. Electronic address: jechoi.9711@gmail.com.
H S JeonThe Molecular Diagnostics & Imaging Research Institute.
M J HongDepartment of Biochemistry and Cell Biology, School of Medicine.
Y Y ChoiDepartment of Biochemistry and Cell Biology, School of Medicine.
H G KangDepartment of Biochemistry and Cell Biology, School of Medicine.
S S YooLung Cancer Center, Kyungpook National University Medical Center, Daegu; Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu.
E B LeeDepartments of Thoracic Surgery.
J Y JeongPathology.
W K LeeBiostatistics Center, School of Medicine, Kyungpook National University, Daegu.
J LeeDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu.
S I ChaDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu.
C H KimDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu.
Y T KimDepartment of Thoracic and Cardiovascular Surgery, Seoul National University School of Medicine, Seoul.
S JheonDepartment of Thoracic and Cardiovascular Surgery, Seoul National University School of Medicine, Seoul.
J W SonDepartment of Internal Medicine, Konyang University Hospital, Daejeon.
J Y ParkLung Cancer Center, Kyungpook National University Medical Center, Daegu; Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu; Department of Biochemistry and Cell Biology, School of Medicine; BK21 Plus KNU Biomedical Convergence Program, Department of Biomedical Science, Kyungpook National University, Daegu, Republic of Korea.
Kyungpook National University · KRSeoul National University · KRKonyang University Hospital · KRKyungpook National University Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) have a key role in carcinogenesis through negative regulation of their target genes. Therefore, genetic variations in miRNAs or their target sites may affect miRNA-mRNA interactions, thereby result in altered expression of target genes. This study was conducted to investigate the associations between single-nucleotide polymorphisms (SNP) located in the miRNA target sites (poly-miRTSs) and survival of patients with early-stage non-small-cell lung cancer (NSCLC).

methodsUsing public SNP database and miRNA target sites prediction program, 354 poly-miRTSs were selected for genotyping. Among these, 154 SNPs applicable to Sequenom's MassARRAY platform were investigated in 357 patients. A replication study was carried out on an independent patient population (n = 479). Renilla luciferase assay and reverse transcription-polymerase chain reaction were conducted to examine functional relevance of potentially functional poly-miRTSs.

resultsOf the 154 SNPs analyzed in a discovery set, 14 SNPs were significantly associated with survival outcomes. Among these, KRT81 rs3660G>C was found to be associated with survival outcomes in the validation cohort. In the combined analysis, patients with the rs3660 GC + CC genotype had a significantly better overall survival compared with those with GG genotype [adjusted hazard ratio (aHR) for OS, 0.65; 95% confidence interval (CI) 0.50-0.85; P = 0.001]. An increased expression of the reporter gene for the C allele of rs3660 compared with the G allele was observed by luciferase assay. Consistently, the C allele was associated with higher relative expression level of KRT81 in tumor tissues.

conclusionThe rs3660G>C affects KRT81 expression and thus influences survival in early-stage NSCLC. The analysis of the rs3660G>C polymorphism may be useful to identify patients at high risk of a poor disease outcome.

Indexed as

Polymorphism, Single Nucleotide3' Untranslated RegionsAgedBinding SitesCarcinoma, Non-Small-Cell LungComputational BiologyDatabases, GeneticFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene FrequencyGenetic Predisposition to DiseaseHEK293 CellsHumansKaplan-Meier EstimateKeratins, Hair-Specific3' Untranslated RegionsKeratins, Hair-SpecificKeratins, Type IIKRT81 protein, humanMicroRNAsRNA, MessengerKRT81miRNA target sitesnon-small cell lung cancerpolymorphisms

Identifiers

PMID25716425
OpenAlexW2172089941

What OpenQuestion holds

Textmetadata
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.