Evidence map›Paper›PMID 24840392›Full record

ArticleJournal of clinical laboratory analysis2015

Association Between Genetic Polymorphism of the MIF Gene and Colorectal Cancer in Taiwan.

Latha Ramireddy, William Tzu-Liang Chen, Ching-Tien Peng, Rouh-Mei Hu, Tao-Wei Ke, Hua-Che Chiang, Sheng-Chi Chang, Fuu-Jen Tsai, Wan-Yu Lo

Open access · bronzeAbstract read
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Article in Journal of clinical laboratory analysis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Latha RamireddyDepartment of Biomedical Informatics, Asia University, Taichung, Taiwan.
William Tzu-Liang ChenDivision of Colorectal Surgery, Department of Surgery, China Medical University Hospital, Taichung, Taiwan.
Ching-Tien PengDepartment of Biomedical Informatics, Asia University, Taichung, Taiwan.
Rouh-Mei HuDepartment of Biomedical Informatics, Asia University, Taichung, Taiwan.
Tao-Wei KeDivision of Colorectal Surgery, Department of Surgery, China Medical University Hospital, Taichung, Taiwan.
Hua-Che ChiangDivision of Colorectal Surgery, Department of Surgery, China Medical University Hospital, Taichung, Taiwan.
Sheng-Chi ChangDivision of Colorectal Surgery, Department of Surgery, China Medical University Hospital, Taichung, Taiwan.
Fuu-Jen TsaiDepartment of Pediatrics, Children's Hospital, China Medical University, Taichung, Taiwan.
Wan-Yu LoDepartment of Medical Research, China Medical University Hospital, Taichung, Taiwan.
China Medical University · TWAsia University · TWChina Medical University Hospital · TWBoston Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is the highest leading cause of cancer-related mortality in Taiwan. Macrophage migration inhibitory factor (MIF) has recently been defined as a novel protumorigenic factor that promotes cell proliferation, migration, and invasion. The aim of the present study is to identify the association between MIF gene polymorphism and CRC.

methodsA case-control study was designed to test the hypothesis. A total of 192 biopsy-diagnosed CRC patients (CRC) and 256 healthy subjects (control) were recruited. Genotyping of four single nucleotide polymorphism (SNPs; rs755662, rs11548059, rs1049829, rs1803976) at chromosome positions 755662 (5' UTR), 11548059 (exon2), 1049829 (exon2), 1803976 (exon3) was performed using a Taqman SNP genotyping assay.

resultsThere is a significant difference in genotype frequency distribution of rs755662 polymorphism between CRC patients and controls (P = 0.011). No significant difference was found in the frequency distribution of rs11548059, rs1049829, rs1803976 polymorphism in CRC patients and controls (P = 0.660, P = 0.700, and P = 0.959, respectively). Moreover, the MIF-173 SNP was also significantly associated with young patients (age < 50 years, P = 0.026) late stage (Stage IV, P = 0.038) and poor differentiation group (P = 0.040). Compared to the control group, the MIF-173 SNP also significantly associated with patients with stages III and IV (P = 0.034 and 0.003, respectively).

conclusionThe presence of MIF-173 (G/C) gene polymorphism (rs755662) was associated with susceptibility, patient age, and stages of CRC in Taiwanese.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAdultAgedAged, 80 and overCase-Control StudiesColorectal NeoplasmsFemaleGene FrequencyHumansIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMaleMiddle AgedNeoplasm StagingPolymorphism, Single NucleotideIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMIF protein, humancolorectal cancergenetic polymorphismsmacrophage migration inhibitory factorsusceptibility

Identifiers

PMID24840392
PMCPMC6806689
OpenAlexW1896869571

What OpenQuestion holds

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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.