Evidence map›Paper›PMID 22428065›Full record

ArticlePloS one2012

Effect of RECK gene polymorphisms on hepatocellular carcinoma susceptibility and clinicopathologic features.

Tsung-Te Chung, Chao-Bin Yeh, Yi-Ching Li, Shih-Chi Su, Ming-Hsien Chien, Shun-Fa Yang, Yi-Hsien Hsieh

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In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

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  12. RECK Gene Polymorphism is Associated with Susceptibility and Prognosis of Wilms' Tumor in Chinese Children.Medical science monitor : international medical journal of experimental and clinical research · 2015
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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 4 institutions in 2 countries.

Tsung-Te ChungInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Chao-Bin Yeh
Yi-Ching Li
Shih-Chi Su
Ming-Hsien Chien
Shun-Fa Yang
Yi-Hsien Hsieh
Chung Shan Medical University · TWChung Shan Medical University Hospital · TWThe University of Texas MD Anderson Cancer Center · USWan Fang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe reversion-inducing-cysteine-rich protein with Kazal motifs (RECK) down-regulation has been confirmed in numerous human cancers and is clinically associated with metastasis. This study investigates the potential associations of RECK single-nucleotide polymorphisms (SNPs) with hepatocellular carcinoma (HCC) susceptibility and its clinicopathologic characteristics. METHODOLOGY/PRINCIPAL

findingsA total of 135 HCC cancer patients and 501 cancer-free controls were analyzed for four RECK SNPs (rs10814325, rs16932912, rs11788747, and rs10972727) using real-time PCR and PCR-RFLP genotyping analysis. After adjusting for other co-variants, the individuals carrying RECK promoter rs10814325 inheriting at least one C allele had a 1.85-fold [95% confidence interval (CI), 1.03-3.36] risk of developing HCC compared to TT wild type carriers. The HCC patients, who carried rs11788747 with at least one G allele, had a higher distant metastasis risk than wild type probands.

conclusionsRECK gene polymorphisms might be a risk factor increasing HCC susceptibility and distant metastasis in Taiwan.

Indexed as

Carcinoma, HepatocellularCase-Control StudiesDNA PrimersGenetic Association StudiesGenetic Predisposition to DiseaseGPI-Linked ProteinsHumansLiver NeoplasmsLogistic ModelsNeoplasm MetastasisPolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideReal-Time Polymerase Chain ReactionRisk FactorsStatistics, NonparametricTaiwanDNA PrimersGPI-Linked ProteinsRECK protein, human

Identifiers

PMID22428065
PMCPMC3299798
OpenAlexW2130932112

What OpenQuestion holds

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LicenceCC BY
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.