Evidence map›Paper›PMID 24254309›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2014

Common genetic variants at 1q22 and 10q23 and gastric cancer susceptibility in a Korean population.

Hye-Rim Song, Hee Nam Kim, Sun-Seog Kweon, Jin-Su Choi, Hyun Jeong Shim, Sang Hee Cho, Ik Joo Chung, Young-Kyu Park, Soo Hyun Kim, Yoo-Duk Choi and 2 more

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 10% 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, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Polymorphism ofFrontiers in oncology · 2021
    Article
  7. Article
  8. Role ofInternational journal of clinical and experimental pathology · 2020
    Article
  9. Article
  10. Article
  11. Single Nucleotide Polymorphisms inFrontiers in oncology · 2018
    Article
  12. Functional polymorphisms inOncotarget · 2017
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Mucin 1 gene (MUC1) and gastric-cancer susceptibility.International journal of molecular sciences · 2014
    Article
  18. 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

12 authors at 4 institutions in 1 country.

Hye-Rim SongDepartment of Preventive Medicine, Chonnam National University Medical School, 5, Hak 1-dong, Dong-gu,, Gwangju, 501-746, South Korea.
Hee Nam Kim
Sun-Seog Kweon
Jin-Su Choi
Hyun Jeong Shim
Sang Hee Cho
Ik Joo Chung
Young-Kyu Park
Soo Hyun Kim
Yoo-Duk Choi
Kyung Woong Joo
Min-Ho Shin
Chonnam National University Hwasun Hospital · KRChonnam National University Hospital · KRChonnam National University · KRGwangju Health University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variants at 1q22 and 10q23 were identified as genetic markers of both gastric cancer and esophageal squamous cell carcinoma susceptibility by two genome-wide association studies. The aim of this study was to determine whether rs4072037A > G in MUC1 at 1q22 and rs2274223A > G in PLCE1 at 10q23 are associated with a risk of gastric cancer in a Korean population. We conducted a large-scale case-control study of 3,245 patients with gastric cancer and 1,700 controls. The allele frequencies of rs4072037G and rs2274223G were 11.2 and 25.5% among patients with gastric cancer, compared with 12.8 and 26.4%, respectively, among controls. We found that the rs4072037 AG genotype was significantly associated with a reduced risk of gastric cancer [odds ratios (OR) = 0.78; 95% confidence interval (CI) = 0.67-0.91 for AG vs AA]. Compared with the rs2274223 AA genotype, we found a significant association between the rs2274223 AG genotype and a weakly reduced risk of gastric cancer (OR = 0.87; 95% CI = 0.76-0.99 for AG vs AA). Our data suggest that genetic variants at 1q22 and 10q23 play a role in gastric carcinogenesis.

Indexed as

Chromosomes, Human, Pair 1Chromosomes, Human, Pair 10Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAgedFemaleGenotypeHumansKoreaMaleMiddle AgedMucin-1Neoplasm StagingPhosphoinositide Phospholipase CStomach NeoplasmsMUC1 protein, humanMucin-1Phosphoinositide Phospholipase Cphospholipase C epsilon

Identifiers

PMID24254309
OpenAlexW1983177439

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.