Evidence map›Paper›PMID 31440867›Full record

ArticleClinical and experimental medicine2019

MicroRNA-15a tissue expression is a prognostic marker for survival in patients with clear cell renal cell carcinoma.

Yulian Mytsyk, Yuriy Borys, Lesia Tumanovska, Dmytro Stroy, Askold Kucher, Katarina Gazdikova, Luis Rodrigo, Peter Kruzliak, Robert Prosecky, Peter Urdzik and 1 more

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Article in Clinical and experimental medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 13 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

11 authors at 6 institutions in 4 countries.

Yulian MytsykDepartment of Urology, Danylo Halytsky Lviv National Medical University, Pekarska str. 69, Lviv, Ukraine.
Yuriy BorysDepartment of Urology, Danylo Halytsky Lviv National Medical University, Pekarska str. 69, Lviv, Ukraine.
Lesia TumanovskaGeneral and Molecular Pathophysiology Department, Bogomoletz Institute of Physiology, National Academy of Sciences, Kiev, Ukraine.
Dmytro StroyGeneral and Molecular Pathophysiology Department, Bogomoletz Institute of Physiology, National Academy of Sciences, Kiev, Ukraine.
Askold KucherDepartment of Radiology, Danylo Halytsky Lviv National Medical University, Lviv, Ukraine.
Katarina GazdikovaDepartment of Nutrition, Faculty of Nursing and Professional Health Studies, Slovak Medical University, Limbova 12, 833 03, Bratislava, Slovakia. katarina.gazdikova@szu.sk.
Luis RodrigoFaculty of Medicine, University of Oviedo and Central University Hospital of Asturias (HUCA), Oviedo, Spain.
Peter KruzliakDepartment of Internal Medicine, Brothers of Mercy Hospital, Polni 3, 63900, Brno, Czech Republic. kruzliakpeter@gmail.com.ORCID http://orcid.org/0000-0002-7069-3784
Robert ProseckyDepartment of Internal Medicine, Brothers of Mercy Hospital, Polni 3, 63900, Brno, Czech Republic.
Peter UrdzikDepartment of Gynaecology and Obstetrics, Faculty of Medicine, Pavol Jozef Safarik University and Louis Pasteur University Hospital, Tr. SNP 1, 04001, Kosice, Slovakia. peter.urdzik@upjs.sk.
Victor DosenkoGeneral and Molecular Pathophysiology Department, Bogomoletz Institute of Physiology, National Academy of Sciences, Kiev, Ukraine.
Bogomoletz Institute of Physiology · UADanylo Halytsky Lviv National Medical University · UAMasaryk University · CZSlovak Medical University · SKUniversidad de Oviedo · ESUniversity of Pavol Jozef Šafárik · SK

Funding

Scientific Grant Agency of the Ministry of Education of the Slovak Republic VEGA 1/0873/18
6 · The paper itself

Abstract

None of the currently investigated molecular markers demonstrated sufficient accuracy in prognostication of the renal cell carcinoma (RCC) oncologic outcomes; thus, none of them has been recommended for the application in the routine clinical practice. The role of miR-15a as a potential prognostic marker for RCC is still not unveiled. The aim of our study was to assess the expression of miR-15a in tumor tissues of the patients with RCC and to evaluate the possibility of its usage as a prognostic molecular biomarker of this disease. The retrospective included 64 adult patients with clear cell RCC (ccRCC) in whom radical or partial nephrectomy was conducted. After deparaffinization of formalin-fixed paraffin-embedded (FFPE) ccRCC specimens, the tissue expression of miR-15a was measured using the reverse transcription and quantitative polymerase chain reaction in the real time. For the reference, the expression of miR-15a was estimated in 15 FFPE tissue specimens of the normal renal parenchyma. Survival analysis involved all cases of non-metastatic RCCs (n = 57). Five-year cancer-specific survival (CSS) was estimated by means of the Kaplan-Meier method and was calculated from the date of surgery to the date of death. Patients with the RCC were characterized by significantly upregulated tumor tissue mean levels of miR-15a compared to the healthy controls: 0.10 ± 2.62 relative units (RU) versus 4.84E - 03 ± 3.11E - 03 RU (p < 0.001). Overexpression of miR-15a was strongly associated with poor histologic prognostic features of ccRCC. Poorly differentiated tumors tend to have more pronounced upregulation of miR-15a compared to highly differentiated lesions: Mean expression values were 4.57 ± 3.19 RU for Fuhrman grade 4 versus 0.02 ± 0.01 RU for Fuhrman grade 1 (p < 0.001). The metastatic involvement of the regional lymphatic nodules (N +) was associated with significantly upregulated miRNA-15a in comparison with N - cases: Mean expression values were 4.92 ± 2.80 RU versus 1.10 ± 2.29 RU, respectively (p < 0.001). In patients with miR-15a expression in RCC tissues ≤ 0.10 RU, mean 5-year CSS was significantly longer compared to patients with expression levels above this threshold: 92.31% (mean duration of survival-59.88 ± 0.12 months) versus 54.8% (mean duration of survival-49.74 ± 2.16 months), respectively (p < 0.001). The tissue expression of miR-15a could be used as a potential prognostic molecular biomarker for conventional RCC.

Indexed as

Up-RegulationBiomarkers, TumorCarcinoma, Renal CellFemaleGene Expression Regulation, NeoplasticHumansKidneyKidney NeoplasmsLymphatic MetastasisMaleMicroRNAsNephrectomyPrognosisRetrospective StudiesSurvival AnalysisTreatment OutcomeBiomarkers, TumorMicroRNAsMIRN15 microRNA, humanBiomarkerCancerClear cellGeneticMicroRNA-15amiRNA-15aPredictionPrognosisRenal cell carcinomaSurvival

Identifiers

PMID31440867
OpenAlexW2969714945

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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.