Evidence map›Paper›PMID 24933103›Full record

ArticlePloS one2014

Associations of polymorphisms in DNA repair genes and MDR1 gene with chemotherapy response and survival of non-small cell lung cancer.

Yan Du, Tong Su, Lijun Zhao, Xiaojie Tan, Wenjun Chang, Hongwei Zhang, Guangwen Cao

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

27 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pharmacogenetic Association betweenBioMed research international · 2020
    Pooled it
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  5. Article
  6. Review
  7. Global trends inFrontiers in oncology · 2023
    Article
  8. Article
  9. Genetic polymorphisms and haplotypes of BRCA1 gene associated with quality of life and survival among patients with non-small-cell lung cancer.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2020
    Article
  10. Article
  11. Inhibition of MDR1 Overcomes Resistance to Brentuximab Vedotin in Hodgkin Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  12. Effect ofAmerican journal of translational research · 2020
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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

7 authors.

Yan DuDepartment of Epidemiology, Second Military Medical University, Shanghai, China.
Tong SuDepartment of Epidemiology, Second Military Medical University, Shanghai, China.
Lijun ZhaoDepartment of Pulmonary Medicine, Changhai Hospital, Second Military Medical University, Shanghai, China.
Xiaojie TanDepartment of Epidemiology, Second Military Medical University, Shanghai, China.
Wenjun ChangDepartment of Epidemiology, Second Military Medical University, Shanghai, China.
Hongwei ZhangDepartment of Epidemiology, Second Military Medical University, Shanghai, China.
Guangwen CaoDepartment of Epidemiology, Second Military Medical University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe aimed to determine the associations of genetic polymorphisms of excision repair cross-complementation group 1 (ERCC1) rs11615, xeroderma pigmentosum group D (XPD/ERCC2) rs13181, X-ray repair cross complementing group 1 (XRCC1) rs25487, XRCC3 rs1799794, and breast cancer susceptibility gene 1 (BRCA1) rs1799966 from the DNA repair pathway and multiple drug resistance 1 (MDR1/ABCB1) rs1045642 with response to chemotherapy and survival of non-small cell lung cancer (NSCLC) in a Chinese population. MATERIALS AND

methodsA total of 352 NSCLC patients were enrolled to evaluate the associations of the six SNPs with response to chemotherapy and overall survival. Logistic regressions were applied to test the associations of genetic polymorphisms with response to chemotherapy in 161 advanced NSCLC patients. Overall survival was analyzed in 161 advanced and 156 early stage NSCLC patients using the Kaplan-Meier method with log-rank test, respectively. Multivariate Cox proportional hazards model was performed to determine the factors independently associated with NSCLC prognosis.

resultsBRCA1 rs1799966 minor allele C (TC+CC vs. TT, OR = 0.402, 95% CI = 0.204-0.794, p = 0.008) and MDR1/ABCB1 rs1045642 minor allele A (GA +AA vs. GG, OR = 0.478, 95% CI = 0.244-0.934, p = 0.030) were associated with a better response to chemotherapy in advanced NSCLC patients. Survival analyses indicated that BRCA1 rs1799966 TC+CC genotypes were associated with a decreased risk of death (HR = 0.617, 95% CI = 0.402-0.948, p = 0.028) in advanced NSCLC patients, and the association was still significant after the adjustment for covariates. Multivariate Cox regression analysis showed that ERCC1 rs11615 AA genotype (P = 0.020) and smoking (p = 0.037) were associated with increased risks of death in early stage NSCLC patients after surgery.

conclusionsPolymorphisms of genes in DNA repair pathway and MDR1 could contribute to chemotherapy response and survival of patients with NSCLC.

Indexed as

Genetic Predisposition to DiseaseAdultAgedAged, 80 and overATP Binding Cassette Transporter, Subfamily BCarcinoma, Non-Small-Cell LungDemographyDNA-Binding ProteinsDNA RepairEndonucleasesFemaleGenetic Association StudiesHumansLung NeoplasmsMaleMiddle AgedABCB1 protein, humanATP Binding Cassette Transporter, Subfamily BDNA-Binding ProteinsEndonucleasesERCC1 protein, human

Identifiers

PMID24933103
PMCPMC4059653

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Registered trials

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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.