Evidence map›Paper›PMID 26177813›Full record

ArticleJournal of cancer research and clinical oncology2016

Replication analysis confirms the association of several variants with acute myeloid leukemia in Chinese population.

Songyu Cao, Guohua Yang, Juan Zhang, Yunfeng Shen, Hongxia Ma, Xifeng Qian, Zhibin Hu

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Replication of a GWAS signal nearBlood neoplasia · 2025
    Article
  2. Review
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 at 1 institution in 1 country.

Songyu CaoDepartment of Epidemiology and Biostatistics, Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Collaborative Innovation Center for Cancer Personalized Medicine, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.
Guohua YangDepartment of Hematology, Wuxi Peoples's Hospital Affiliated to Nanjing Medical University, No. 299 Qingyang Road, Wuxi, 214194, China.
Juan ZhangDepartment of Hematology, Wuxi Peoples's Hospital Affiliated to Nanjing Medical University, No. 299 Qingyang Road, Wuxi, 214194, China.
Yunfeng ShenDepartment of Hematology, Wuxi Peoples's Hospital Affiliated to Nanjing Medical University, No. 299 Qingyang Road, Wuxi, 214194, China.
Hongxia MaDepartment of Epidemiology and Biostatistics, Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Collaborative Innovation Center for Cancer Personalized Medicine, School of Public Health, Nanjing Medical University, Nanjing, 211166, China. hongxiama@njmu.edu.cn.
Xifeng QianDepartment of Hematology, Wuxi Peoples's Hospital Affiliated to Nanjing Medical University, No. 299 Qingyang Road, Wuxi, 214194, China. greenleafchemical@163.com.
Zhibin HuDepartment of Epidemiology and Biostatistics, Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Collaborative Innovation Center for Cancer Personalized Medicine, School of Public Health, Nanjing Medical University, Nanjing, 211166, China. zhibin_hu@njmu.edu.cn.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTwo genome-wide association studies (GWASs) have identified several new acute leukemia susceptibility loci in populations of European descent. However, the roles of these loci in the development of acute leukemia in other populations are largely unknown.

methodsWe genotyped 16 single-nucleotide polymorphisms selected from published GWASs in an independent case-control study with a total of 545 acute myeloid leukemia (AML) cases and 1034 cancer-free controls in a Chinese population. Multivariate logistic regression was used to analyze the associations between these variants and AML risk.

resultsWe found that with the similar effect to GWASs, risk alleles of rs2191566, rs9290663, rs11155133, rs2239633, rs10821936, and rs2242041 significantly increased the risk of AML in at least one genetic model [odds ratios (ORs) range from 1.26 to 4.34, P values range from <0.001 to 0.043]. However, the variant T allele of rs10873876 decreased the AML risk, which was in the opposite effect direction (OR 0.62, P < 0.001 in additive model). Besides, we found significant multiplicative interaction between rs9290663 and age (≤45 years old and >45 years old; P = 0.009).

conclusionOur results indicated that genetic variants associated with acute leukemia risk in European populations may also play important roles in AML development in Chinese population.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyAdultAsian PeopleBiomarkers, TumorCase-Control StudiesChinaFemaleGenotypeHumansLeukemia, Myeloid, AcuteMaleMiddle AgedNeoplasm StagingPolymorphism, Single NucleotidePrognosisBiomarkers, TumorLeukemiaPolymorphismSusceptibility

Identifiers

PMID26177813
PMCPMC11819256
OpenAlexW2108384307

What OpenQuestion holds

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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.