Evidence map›Paper›PMID 24654646›Full record

ArticleCancer science2014

Genetic variants at 8q24 are associated with risk of esophageal squamous cell carcinoma in a Chinese population.

Ningbin Dai, Mingfeng Zheng, Cheng Wang, Yong Ji, Jiangbo Du, Chen Zhu, Yisha He, Meng Zhu, Xun Zhu, Min Sun and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
3.8field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Contribution ofPharmacogenomics and personalized medicine · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Functional polymorphisms inOncotarget · 2017
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Amplification and overexpression ofInternational journal of medical sciences · 2016
    Article
  14. Article
  15. Article
  16. 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

17 authors at 4 institutions in 1 country.

Ningbin DaiDepartment of Epidemiology and Biostatistics and Ministry of Education Key Laboratory of Modern Toxicology, School of Public Health, Nanjing Medical University, Nanjing, China; Section of Clinical Epidemiology, Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Cancer Center, Nanjing Medical University, Nanjing, China.
Mingfeng Zheng
Cheng Wang
Yong Ji
Jiangbo Du
Chen Zhu
Yisha He
Meng Zhu
Xun Zhu
Min Sun
Juncheng Dai
Hongxia Ma
Jingyu Chen
Zhibin Hu
Haiyong Gu
Guangfu Jin
Hongbing Shen
Nanjing Medical University · CNAffiliated Hospital of Jiangsu University · CNJiangsu Cancer Hospital · CNWuxi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esophageal cancer and gastric cancer have shared risk factors and inherited susceptibility. Recent genome-wide association studies have identified multiple genetic loci associated with gastric cancer risk, which may also involve in the development of esophageal cancer. Herein, we evaluated the relationship of gastric cancer risk-related variants at 1q22, 3q13.3, 5p13.1, and 8q24 with the risk of esophageal squamous cell carcinoma (ESCC) in a Chinese population with a case-control study (2139 cases and 2273 controls). We found that the T allele of rs2294008, an intronic variant of the PSCA gene at 8q24 that was previously associated with an increased risk of gastric cancer, was inversely associated with a decreased risk of ESCC (odds ratio = 0.90; 95% confidence interval, 0.81-0.99; P = 0.034). Of interest, the association of rs2294008 with ESCC was consistent with that observed in esophageal adenocarcinoma and ESCC in Caucasian populations. However, no significant associations were observed for the other three variants at 1q22 (rs4072037), 3q13.31 (rs9841504), and 5p13.1 (rs13361707). Our findings suggest that the susceptibility locus of PSCA at 8q24 may be a double-edged sword, as modulator between the carcinogenesis processes of stomach and esophagus.

Indexed as

AdenocarcinomaAntigens, NeoplasmCarcinoma, Squamous CellCase-Control StudiesChinaChromosomes, Human, Pair 8Esophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleGene FrequencyGenetic Predisposition to DiseaseGenetic VariationGenome-Wide Association StudyGenotypeGPI-Linked ProteinsHumansAntigens, NeoplasmGPI-Linked ProteinsNeoplasm ProteinsPSCA protein, human8q24esophageal cancergastric cancergenome-wide association studiesPSCA

Identifiers

PMID24654646
PMCPMC4317888
OpenAlexW2015366551

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.