Evidence map›Paper›PMID 31564221›Full record

ArticleTechnology in cancer research & treatment2019

Radiogenomics in Clear Cell Renal Cell Carcinoma: Correlations Between Advanced CT Imaging (Texture Analysis) and MicroRNAs Expression.

Chiara Marigliano, Stefano Badia, Davide Bellini, Marco Rengo, Damiano Caruso, Claudia Tito, Selenia Miglietta, Giovanni Palleschi, Antonio Luigi Pastore, Antonio Carbone and 3 more

Abstract read
In one paragraph

Article in Technology in cancer research & treatment, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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  5. Phenomic Imaging.Phenomics (Cham, Switzerland) · 2023
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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

13 authors.

Chiara MariglianoDepartment of Radiological, Oncological and Pathological Sciences, University of Rome "Sapienza"-Polo Pontino, ICOT Hospital, Latina, Italy.ORCID 0000-0002-3592-4073
Stefano BadiaDepartment of Radiological, Oncological and Pathological Sciences, University of Rome "Sapienza"-Polo Pontino, ICOT Hospital, Latina, Italy.
Davide BelliniDepartment of Radiological, Oncological and Pathological Sciences, University of Rome "Sapienza"-Polo Pontino, ICOT Hospital, Latina, Italy.
Marco RengoDepartment of Radiological, Oncological and Pathological Sciences, University of Rome "Sapienza"-Polo Pontino, ICOT Hospital, Latina, Italy.ORCID 0000-0001-9087-5692
Damiano CarusoDepartment of Radiological, Oncology and Pathology Sciences, "Sapienza" University of Rome, Italy Radiology Unit, Sant'Andrea University Hospital, Rome, Italy.
Claudia TitoDepartment of Anatomical, Histological, Forensic & Orthopaedic Sciences, Section of Histology & Medical Embryology, "Sapienza" University of Rome, Laboratory Affiliated With Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Selenia MigliettaDepartment of Anatomy, Histology, Forensic Medicine and Orthopaedics, Section of Anatomy, Electron Microscopy Unit, Laboratory "Pietro M. Motta," "Sapienza" University of Rome, Rome, Italy.
Giovanni PalleschiDepartment of Medical-Surgical Sciences and Biotechnologies, "Sapienza" University of Rome, Urology Unit ICOT, Latina, Italy.
Antonio Luigi PastoreDepartment of Medical-Surgical Sciences and Biotechnologies, "Sapienza" University of Rome, Urology Unit ICOT, Latina, Italy.
Antonio CarboneDepartment of Medical-Surgical Sciences and Biotechnologies, "Sapienza" University of Rome, Urology Unit ICOT, Latina, Italy.
Francesco FaziDepartment of Anatomical, Histological, Forensic & Orthopaedic Sciences, Section of Histology & Medical Embryology, "Sapienza" University of Rome, Laboratory Affiliated With Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Vincenzo PetrozzaDepartment of Medical-Surgical Sciences and Biotechnologies, "Sapienza" University of Rome, Urology Unit ICOT, Latina, Italy.
Andrea LaghiDepartment of Radiological, Oncology and Pathology Sciences, "Sapienza" University of Rome, Italy Radiology Unit, Sant'Andrea University Hospital, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA relevant challenge for the improvement of clear cell renal cell carcinoma management could derive from the identification of novel molecular biomarkers that could greatly improve the diagnosis, prognosis, and treatment choice of these neoplasms. In this study, we investigate whether quantitative parameters obtained from computed tomography texture analysis may correlate with the expression of selected oncogenic microRNAs.

methodsIn a retrospective single-center study, multiphasic computed tomography examination (with arterial, portal, and urographic phases) was performed on 20 patients with clear cell renal cell carcinoma and computed tomography texture analysis parameters such as entropy, kurtosis, skewness, mean, and standard deviation of pixel distribution were measured using multiple filter settings. These quantitative data were correlated with the expression of selected microRNAs (miR-21-5p, miR-210-3p, miR-185-5p, miR-221-3p, miR-145-5p). Both the evaluations (microRNAs and computed tomography texture analysis) were performed on matched tumor and normal corticomedullar tissues of the same patients cohort.

resultsIn this pilot study, we evidenced that computed tomography texture analysis has robust parameters (eg, entropy, mean, standard deviation) to distinguish normal from pathological tissues. Moreover, a higher coefficient of determination between entropy and miR-21-5p expression was evidenced in tumor versus normal tissue. Interestingly, entropy and miR-21-5p show promising correlation in clear cell renal cell carcinoma opening to a radiogenomic strategy to improve clear cell renal cell carcinoma management.

conclusionIn this pilot study, a promising correlation between microRNAs and computed tomography texture analysis has been found in clear cell renal cell carcinoma. A clear cell renal cell carcinoma can benefit from noninvasive evaluation of texture parameters in adjunction to biopsy results. In particular, a promising correlation between entropy and miR-21-5p was found.

Indexed as

GenomicsTomography, X-Ray ComputedAgedBiomarkers, TumorCarcinoma, Renal CellFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImage Processing, Computer-AssistedKidney NeoplasmsMaleMicroRNAsMiddle AgedNeoplasm StagingRetrospective StudiesBiomarkers, TumorMicroRNAsmicroRNAradiogenomicsrenal cell carcinomatexture analysis

Identifiers

PMID31564221
PMCPMC6767738

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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.