Evidence map›Paper›PMID 25755792›Full record

ArticleInternational journal of clinical and experimental pathology2015

Investigation on the DNA repaired gene polymorphisms and response to chemotherapy and overall survival of osteosarcoma.

Wei-Ping Ji, Neng-Bin He

Open access · greenAbstract read
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 19 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 4 pooled it
3.6field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 4 syntheses or guidelines pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Review
  6. Review
  7. Article
  8. Cancers · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Observational
  14. Association between common polymorphisms inOncoTargets and therapy · 2018
    Article
  15. Article
  16. Review
  17. Article
  18. The pharmacogenomics of osteosarcoma.The pharmacogenomics journal · 2017
    Review
  19. 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

2 authors at 1 institution in 1 country.

Wei-Ping JiDepartment of Orthopedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital Shanghai, China.
Neng-Bin HeDepartment of Orthopedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital Shanghai, China.
Shanghai Sixth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to evaluate the influence of polymorphisms in NER and HRR pathways on the response to cisplatin-based treatment and clinical outcome in osteosarcoma patients. 214 osteosarcoma patients treated with cisplatin-based chemotherapy were collected between January 2008 and January 2011. Genotypes of ERCC1 rs11615, ERCC2 rs1799793 and rs13181, NBN rs709816, RAD51 rs1801320, and XRCC3 rs861539 were conducted by Polymerase Chain Reaction Restriction Fragment Length Polymorphism (PCR-RFLP) assay. By conditional logistic regression analysis, patients carrying CC genotype of ERCC1 rs11615 showed a significant more good responder than TT genotype, and the OR (95% CI) was 2.51 (1.02-6.85). In the Cox proportional hazards model, after adjusting for potential confounding factors, we found that individuals carrying CC genotype of ERCC1 rs11615 was associated with decreased risk of death from osteosarcoma, and the HR (95% CI) was 0.43 (0.15-0.93). In conclusion, our results suggest that ERCC1 rs11615 polymorphism in the DNA repair pathways play an important role in the response to chemotherapy and overall survival of osteosarcoma.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultBone NeoplasmsCell Cycle ProteinsChildDNA-Binding ProteinsDNA RepairDrug Resistance, NeoplasmEndonucleasesFemaleGenotypeHumansKaplan-Meier EstimateMaleNuclear ProteinsCell Cycle ProteinsDNA-Binding ProteinsEndonucleasesERCC1 protein, humanERCC2 protein, humanNBN protein, humanNuclear ProteinsRAD51 protein, humanRad51 RecombinaseXeroderma Pigmentosum Group D ProteinX-ray repair cross complementing protein 3ERCC1 rs11615osteosarcomaoverall survivalpolymorphismresponse to chemotherapy

Identifiers

PMID25755792
PMCPMC4348835
OpenAlexW102310467

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.