Evidence map›Paper›PMID 31469874›Full record

ArticlePloS one2019

MicroRNA regulation in colorectal cancer tissue and serum.

Lukasz Gmerek, Kari Martyniak, Karolina Horbacka, Piotr Krokowicz, Wojciech Scierski, Pawel Golusinski, Wojciech Golusinski, Augusto Schneider, Michal M Masternak

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 40 citations in OpenAlex.

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  13. Dynamic liquid biopsy components as predictive and prognostic biomarkers in colorectal cancer.Journal of experimental & clinical cancer research : CR · 2022
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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 3 countries.

Lukasz GmerekCollege of Medicine, Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, United States of America.
Kari MartyniakCollege of Medicine, Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, United States of America.
Karolina HorbackaDepartment of General and Colorectal Surgery, Poznan University of Medical Sciences, Poznan, Poland.
Piotr KrokowiczDepartment of General and Colorectal Surgery, Poznan University of Medical Sciences, Poznan, Poland.
Wojciech ScierskiDepartment of Otorhinolaryngology and Laryngological Oncology in Zabrze, Medical University of Silesia, Katowice, Poland.
Pawel GolusinskiDepartment of Otolaryngology and Maxillofacial Surgery, University of Zielona Gora, Zielona Gora, Poland.
Wojciech GolusinskiDepartment of Head and Neck Surgery, Poznan University of Medical Sciences, The Greater Poland Cancer Centre, Poznan, Poland.
Augusto SchneiderFaculdade de Nutrição, Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Michal M MasternakCollege of Medicine, Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, United States of America.ORCID 0000-0002-8483-930X
Poznan University of Medical Sciences · PLUniversity of Central Florida · USMedical University of Silesia · PLUniversidade Federal de Pelotas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer is recognized as the fourth leading cause of cancer-related deaths worldwide. Thus, there is ongoing search for potential new biomarkers allowing quicker and less invasive detection of the disease and prediction of the treatment outcome. Therefore, the aim of our study was to identify colorectal cancer specific miRNAs expressed in cancerous and healthy tissue from the same patient and to further correlate the presence of the same miRNAs in the circulation as potential biomarkers for diagnosis. In the current study we detected a set of 40 miRNAs differentially regulated in tumor tissue when comparing with healthy tissue. Additionally, we found 8 miRNAs differentially regulated in serum of colorectal cancer patients. Interestingly, there was no overlap in miRNAs regulated in tissue and serum, suggesting that serum regulated miRNAs may be not actively secreted from colorectal tumor cells. However, four of differentially expressed miRNAs, including miR-21, miR-17, miR-20a and miR-32 represent the miRNAs characteristic for different tumor types, including breast, colon, lung, pancreas, prostate and stomach cancer. This finding suggests important groups of miRNAs which can be further validated as markers for diagnosis of tumor tissue and regulation of carcinogenesis.

Indexed as

Biomarkers, TumorCirculating MicroRNAAdultAgedCase-Control StudiesColorectal NeoplasmsComputational BiologyGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMicroRNAsMiddle AgedBiomarkers, TumorCirculating MicroRNAMicroRNAs

Identifiers

PMID31469874
PMCPMC6716664
OpenAlexW2970051875

What OpenQuestion holds

Textmetadata
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.