Evidence map›Paper›PMID 31376327›Full record

ArticleCell journal2020

CD44 Gene rs8193 C Allele Is Significantly Enriched in Gastric Cancer Patients.

Roya Mokhtarian, Hossein Tabatabaeian, Pardis Saadatmand, Mansoureh Azadeh, Negar Balmeh, Bagher Yakhchali, Kamran Ghaedi

Open access · greenAbstract read
In one paragraph

Article in Cell journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 21 citations in OpenAlex.

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  6. Immune Response-Related Genes -Pharmacogenomics and personalized medicine · 2020
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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 2 countries.

Roya MokhtarianDivision of Cellular and Molecular Biology, Department of Biology, NourDanesh Institute of Higher Education, Meymeh, Iran.
Hossein TabatabaeianDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Pardis SaadatmandZistFanavari Novin Biotechnology Institute, Isfahan, Iran.
Mansoureh AzadehZistFanavari Novin Biotechnology Institute, Isfahan, Iran.
Negar BalmehDivision of Cellular and Molecular Biology, Department of Biology, NourDanesh Institute of Higher Education, Meymeh, Iran.
Bagher YakhchaliInstitute of Industrial and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology Institute, Tehran, Iran.
Kamran GhaediDepartment of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
University of Isfahan · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGastric cancer is a multifactorial disease. In addition to environmental factors, many genes are involved in this malignancy. One of the genes associated with gastric cancer is MATERIALS AND

methodsIn this cross-sectional case-control study, rs8193 polymorphism was genotyped by allele specific primer polymerase chain reaction (ASP-PCR) technique. The obtained data were statistically analyzed. To find the potential mechanism of action, rs8193 was bioinformatically investigated.

resultsrs8193 C allele played a risk factor role for gastric cancer. Patients carrying this allele were more susceptible to have gastric cancer, with lymph node spread. On the other hand, rs8193 T allele, a protective factor, was associated with a higher chance of accumulation in the lower stages of cancer. C allele might impose its effect via destabilizing

conclusionrs8193 is statistically associated with the risk of malignancy, lymph node spread and stage of gastric cancer in Iranian population.

Indexed as

CD44Gastric CancermiR-570

Identifiers

PMID31376327
PMCPMC6722445
OpenAlexW2981014064

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.