Evidence map›Paper›PMID 23951214›Full record

ArticlePloS one2013

Functional polymorphisms in FAS/FASL system increase the risk of neuroblastoma in Chinese population.

Wei Han, Yuling Zhou, Rong Zhong, Chen Wu, Ranran Song, Li Liu, Li Zou, Yan Qiao, Kan Zhai, Jiang Chang and 9 more

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. CD95 rs1800682A/G variant and tumor risk in Asians: evidence from a meta-analysis of 36 case-control studies containing 22,438 samples.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Pooled it
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  6. OncoTargets and therapy · 2020
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  7. Oxidative medicine and cellular longevity · 2019
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  11. Journal of Cancer · 2018
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  12. Oncotarget · 2017
    Article
  13. TheAging · 2017
    Article
  14. [Research progress of microRNA and its non-viral vector in intervertebral disc degeneration].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2017
    Review
  15. Common variations withinOncoTargets and therapy · 2017
    Article
  16. OncoTargets and therapy · 2017
    Article
  17. Article
  18. Article
  19. Role of microRNA-210 in human intervertebral disc degeneration.Experimental and therapeutic medicine · 2016
    Article
  20. 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

19 authors.

Wei HanDepartment of Surgical Oncology, Beijing Children's Hospital affiliated to Capital Medical University, Beijing, China.
Yuling Zhou
Rong Zhong
Chen Wu
Ranran Song
Li Liu
Li Zou
Yan Qiao
Kan Zhai
Jiang Chang
Liming Huang
Li Liu
Xuzai Lu
Jiao Lou
Dianke Yu
Wen Tan
Jinzhe Zhang
Huanmin Wang
Xiaoping Miao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The FAS and FASL system plays a substantial role in apoptosis and immune escape of cells. Three polymorphisms located in the promoter regions of FAS (-1377G/A and -670A/G) and FASL (-844T/C) have been shown to alter the transcriptional activity of the genes, respectively. This study was conducted to evaluate the effects of these polymorphisms on the susceptibility of neuroblastoma in the Chinese population. A total of 203 patients with neuroblastoma and 411 controls were recruited in this case-control study. Polymerase chain reaction-based restriction fragment length polymorphism (PCR-RFLP) was applied for genotyping. Unconditional logistic regression was used to estimate cancer risk by calculating odds ratios (ORs) and their 95% confidence intervals (95% CIs). It was observed that significantly increased risks of neuroblastoma associated with FAS -1377G/A and FASL -844T/C polymorphisms, with ORs equal to 1.55 (95% CI, 1.10-2.20) for FAS -1377 A allele and 2.90 (95% CI, 2.04-4.12) for FASL -844CC genotype carriers compared with non-carriers, respectively. However, no association was found between the polymorphisms of FAS -670A/G and risk of neuroblastoma. In addition, the cumulative effect of FAS and FASL polymorphisms on risk of neuroblastoma was observed (P for trend = 2.502×10(-10)), with OR for the carriers of both FAS -1377A allele and FASL -844CC genotypes equaled to 3.95 (95% CI, 2.40-6.51). This work reveals that polymorphisms of FAS -1377G/A and FASL -844T/C but not FAS -670A/G are associated with risk of neuroblastoma in Chinese. These findings support the hypothesis that genetic polymorphism in FAS/FASL death system may influence individual susceptibility to neuroblastoma.

Indexed as

Polymorphism, Single NucleotideAdultAgedAllelesAsian PeopleCase-Control StudiesChild, PreschoolChinaFas Ligand Proteinfas ReceptorFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansInfantFas Ligand Proteinfas Receptor

Identifiers

PMID23951214
PMCPMC3741122

What OpenQuestion holds

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LicenceCC BY
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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.