Evidence map›Paper›PMID 21226972›Full record

ArticleBMC medical genomics2011

Gastric cancers of Western European and African patients show different patterns of genomic instability.

Tineke E Buffart, Melanie Louw, Nicole C T van Grieken, Marianne Tijssen, Beatriz Carvalho, Bauke Ylstra, Heike Grabsch, Chris J J Mulder, Cornelis J H van de Velde, Schalk W van der Merwe and 1 more

Abstract readComparative Study
In one paragraph

Article in BMC medical genomics, 2011. 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
–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

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

  1. Pooled it
  2. Article
  3. Review
  4. Gastric Cancer Cell Lines Have DifferentCanadian journal of gastroenterology & hepatology · 2018
    Article
  5. Expression of Mismatch Repair Proteins in Early and Advanced Gastric Cancer in Poland.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  6. Article
  7. Review
  8. Review
  9. Pathogenetic mechanisms in gastric cancer.World journal of gastroenterology · 2014
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Incidence trends and mortality rates of gastric cancer in Israel.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2013
    Article
  15. Article
  16. Genetic aspects of gastric cancer instability.TheScientificWorldJournal · 2012
    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

11 authors.

Tineke E BuffartDept. of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Melanie Louw
Nicole C T van Grieken
Marianne Tijssen
Beatriz Carvalho
Bauke Ylstra
Heike Grabsch
Chris J J Mulder
Cornelis J H van de Velde
Schalk W van der Merwe
Gerrit A Meijer

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfection with H. pylori is important in the etiology of gastric cancer. Gastric cancer is infrequent in Africa, despite high frequencies of H. pylori infection, referred to as the African enigma. Variation in environmental and host factors influencing gastric cancer risk between different populations have been reported but little is known about the biological differences between gastric cancers from different geographic locations. We aim to study genomic instability patterns of gastric cancers obtained from patients from United Kingdom (UK) and South Africa (SA), in an attempt to support the African enigma hypothesis at the biological level.

methodsDNA was isolated from 67 gastric adenocarcinomas, 33 UK patients, 9 Caucasian SA patients and 25 native SA patients. Microsatellite instability and chromosomal instability were analyzed by PCR and microarray comparative genomic hybridization, respectively. Data was analyzed by supervised univariate and multivariate analyses as well as unsupervised hierarchical cluster analysis.

resultsTumors from Caucasian and native SA patients showed significantly more microsatellite instable tumors (p < 0.05). For the microsatellite stable tumors, geographical origin of the patients correlated with cluster membership, derived from unsupervised hierarchical cluster analysis (p = 0.001). Several chromosomal alterations showed significantly different frequencies in tumors from UK patients and native SA patients, but not between UK and Caucasian SA patients and between native and Caucasian SA patients.

conclusionsGastric cancers from SA and UK patients show differences in genetic instability patterns, indicating possible different biological mechanisms in patients from different geographical origin. This is of future clinical relevance for stratification of gastric cancer therapy.

Indexed as

Genomic InstabilityAdultAfricaAgedAged, 80 and overBlack PeopleChromosomal InstabilityComparative Genomic HybridizationFemaleHumansMaleMicrosatellite InstabilityMicrosatellite RepeatsMiddle AgedSouth AfricaStomach Neoplasms

Identifiers

PMID21226972
PMCPMC3033789

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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.