Evidence map›Paper›PMID 27110571›Full record

ArticleBioMed research international2016

Expression of Migration-Related Genes in Human Colorectal Cancer and Activity of a Disintegrin and Metalloproteinase 17.

Katarzyna Walkiewicz, Paweł Kozieł, Martyna Bednarczyk, Adam Błażelonis, Urszula Mazurek, Małgorzata Muc-Wierzgoń

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  12. Extracellular Matrix Biomarkers in Colorectal Cancer.International journal of molecular sciences · 2021
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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

6 authors at 1 institution in 1 country.

Katarzyna WalkiewiczDepartment of Internal Medicine, Faculty of Public Health in Bytom, Medical University of Silesia, 40-055 Katowice, Poland.
Paweł KoziełDepartment of Internal Medicine, Faculty of Public Health in Bytom, Medical University of Silesia, 40-055 Katowice, Poland.
Martyna BednarczykDepartment of Internal Medicine, Faculty of Public Health in Bytom, Medical University of Silesia, 40-055 Katowice, Poland.
Adam BłażelonisDepartment of Internal Medicine, Faculty of Public Health in Bytom, Medical University of Silesia, 40-055 Katowice, Poland.
Urszula MazurekDepartment of Molecular Biology, Faculty of Pharmacy in Sosnowiec, Medical University of Silesia, 40-055 Katowice, Poland.
Małgorzata Muc-WierzgońDepartment of Internal Medicine, Faculty of Public Health in Bytom, Medical University of Silesia, 40-055 Katowice, Poland.
Medical University of Silesia · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe ability to form metastases which depends on the mechanisms of cell migration is an important element of the progression of cancer. In the present study we analyzed the genes involved in the regulation of migration in colon cancer cells. MATERIALS AND

methodsA total of 20 pairs of surgically removed tumoral and healthy (marginal) tissues samples from colorectal cancer patients at clinical stages I-II and III-IV were analyzed. The isolation of RNA from CRC and normal tissues and its subsequent molecular analysis were performed according to manufacturer's instructions. Microarray data analysis was performed using the GeneSpring 11.5 platform and Significance Analysis of Microarrays (SAM). In SAM analysis to identify significantly differentially expressed genes score and q-value parameters were used.

resultsThe largest increase in expression of genes was shown by MMP9, ADAM17, EphA2, and TIMP.

conclusionsPresented genes, especially ADAM17, MMP9, EphA2, TIMP1, ICAM 11, and CD4, may be used as prognostic markers of advanced stages of colorectal cancer, contributing to the development of new lines of therapy focused on reducing metastasis of the primary tumor.

Indexed as

ADAM17 ProteinBiomarkers, TumorCell MovementColorectal NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMaleMatrix Metalloproteinase 9Microarray AnalysisNeoplasm MetastasisNeoplasm StagingReceptor, EphA2Tissue Inhibitor of MetalloproteinasesADAM17 ProteinADAM17 protein, humanBiomarkers, TumorMatrix Metalloproteinase 9MMP9 protein, humanReceptor, EphA2Tissue Inhibitor of Metalloproteinases

Identifiers

PMID27110571
PMCPMC4826671
OpenAlexW2304416662

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.