Evidence map›Paper›PMID 26191265›Full record

ArticleInternational journal of clinical and experimental pathology2015

Genetic variability of genes in NER pathway influences the treatment outcome of gastric cancer.

Ming-Hui Xue, Guang-Yan Li, Xin-Jun Wu, Chao-Xian Zhang, Cai-Feng Zhang, Kong-Xi Zhu

Open access · greenAbstract readComparative Study
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
3.8field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Relationship betweenMedicina (Kaunas, Lithuania) · 2024
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Article
  7. Review
  8. Article
  9. Effect ofOncoTargets and therapy · 2019
    Article
  10. Article
  11. OncoTargets and therapy · 2018
    Article
  12. International journal of molecular epidemiology and genetics · 2018
    Article
  13. Polymorphisms in DNA repair genes in gastrointestinal stromal tumours: susceptibility and correlation with tumour characteristics and clinical outcome.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  14. Article
  15. Article
  16. Article
  17. Genetic variability of ERCC1 genes in NER pathway influences the treatment outcome of gastric cancer.International journal of clinical and experimental pathology · 2015
    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.

Ming-Hui XueDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Xinxiang Medical University Weihui 453100, China.
Guang-Yan LiDepartment of Gastroenterology, The First Affiliated Hospital of Xinxiang Medical University Weihui 453100, China.
Xin-Jun WuDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Xinxiang Medical University Weihui 453100, China.
Chao-Xian ZhangDepartment of Gastroenterology, The First Affiliated Hospital of Xinxiang Medical University Weihui 453100, China.
Cai-Feng ZhangDepartment of Gastroenterology, The First Affiliated Hospital of Xinxiang Medical University Weihui 453100, China.
Kong-Xi ZhuDepartment of Gastroenterology, The Second Hospital, Shandong University Jinan 250033, China.
First Affiliated Hospital of Xinxiang Medical University · CNSichuan University · CNXinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We performed a study to investigate the role of ERCC1, ERCC2, ERCC5, XPA and XPC polymorphisms from perspective of the whole NER pathway in the prognosis of gastric cancer. A total of 410 gastric cancer patients were recruited between January 2010 and December 2011. Restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR) was used to analyze genotypes of ERCC1 rs11615 and rs3212986, ERCC2 rs13181 and s1799793, ERCC5 rs17655, XPA rs1800975 and XPC rs2228001. Our study found that carriers of ERCC1 rs3212986 TT genotype showed significantly favorable survival than wide-type GG genotype in multivariate analysis (OR=6.38, 95% CI=2.54-19.03), and patients with variant CC genotype of ERCC2 rs13181 exhibited better response to chemotherapy than those with AA genotype (OR=2.21, 95% CI=1.17-4.25). By Cox proportional hazards model, patients with variant TT genotype of ERCC1 rs3212986 exhibited longer PFS and OS than those who had GG genotype (for PFS, HR=0.37, 95% CI=0.17-0.75; for OS, HR=0.36, 95% CI=0.13-0.87). For ERCC2 rs13181 polymorphism, carriers with CC genotype demonstrated significantly increased hazards of progression of disease and death in multivariate model (for PFS, HR=0.48, 95% CI=0.26-0.88; for OS, HR=0.44, 95% CI=0.20-0.91). In conclusion, our finding suggests that ERCC1 rs3212986 and ERCC2 rs13181 gene polymorphism could influence the response to chemotherapy and clinical outcome of gastric cancer.

Indexed as

Polymorphism, Single NucleotideAdultAgedAmplified Fragment Length Polymorphism AnalysisBiomarkers, TumorDisease-Free SurvivalDisease ProgressionDNA-Binding ProteinsDNA RepairEndonucleasesFemaleGene FrequencyGenetic Predisposition to DiseaseHeterozygoteHomozygoteHumansBiomarkers, TumorDNA-Binding ProteinsEndonucleasesERCC1 protein, humanERCC2 protein, humanXeroderma Pigmentosum Group D Proteinclinical outcomeDNA repair genegastric cancerpolymorphism

Identifiers

PMID26191265
PMCPMC4503136
OpenAlexW2419540226

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.