Evidence map›Paper›PMID 34058987›Full record

ArticleBMC bioinformatics2021

A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients.

Eskezeia Y Dessie, Jeffrey J P Tsai, Jan-Gowth Chang, Ka-Lok Ng

Abstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. miR-378a-3p promotes renal cell carcinoma proliferation, migration, and invasion by targeting TOB2.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  7. Superstorm Sandy exposureFrontiers in neuroscience · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Epigenetic Biomarkers of Renal Cell Carcinoma for Liquid Biopsy Tests.International journal of molecular sciences · 2021
    Review
  12. Article
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

4 authors.

Eskezeia Y DessieDepartment of Bioinformatics and Medical Engineering, Asia University, Taichung, Taiwan.
Jeffrey J P TsaiDepartment of Bioinformatics and Medical Engineering, Asia University, Taichung, Taiwan.
Jan-Gowth ChangDepartment of Laboratory Medicine, China Medical University, Taichung, Taiwan. d6781@mail.cmuh.org.tw.
Ka-Lok NgDepartment of Bioinformatics and Medical Engineering, Asia University, Taichung, Taiwan. ppiddi@gmail.com.ORCID http://orcid.org/0000-0001-6315-6326

Funding

Asia University 106-asia-06, 106-asia-09, 107-asia-02 and 107-asia-09China Medical University Hospital DMR-107-209Ministry of Science and Technology, Taiwan MOST 109-2221-E-468-013, MOST 109-2221-E-150-036 and MOST 108-2221-E-468-020
6 · The paper itself

Abstract

backgroundClear cell renal cell carcinoma (ccRCC) is the most common subtype of renal carcinoma and patients at advanced stage showed poor survival rate. Despite microRNAs (miRNAs) are used as potential biomarkers in many cancers, miRNA biomarkers for predicting the tumor stage of ccRCC are still limitedly identified. Therefore, we proposed a new integrated machine learning (ML) strategy to identify a novel miRNA signature related to tumor stage and prognosis of ccRCC patients using miRNA expression profiles. A multivariate Cox regression model with three hybrid penalties including Least absolute shrinkage and selection operator (Lasso), Adaptive lasso and Elastic net algorithms was used to screen relevant prognostic related miRNAs. The best subset regression (BSR) model was used to identify optimal prognostic model. Five ML algorithms were used to develop stage classification models. The biological significance of the miRNA signature was analyzed by utilizing DIANA-mirPath.

resultsA four-miRNA signature associated with survival was identified and the expression of this signature was strongly correlated with high risk patients. The high risk patients had unfavorable overall survival compared with the low risk group (HR = 4.523, P-value = 2.86e-08). Univariate and multivariate analyses confirmed independent and translational value of this predictive model. A combined ML algorithm identified six miRNA signatures for cancer staging prediction. After using the data balancing algorithm SMOTE, the Support Vector Machine (SVM) algorithm achieved the best classification performance (accuracy = 0.923, sensitivity = 0.927, specificity = 0.919, MCC = 0.843) when compared with other classifiers. Furthermore, enrichment analysis indicated that the identified miRNA signature involved in cancer-associated pathways.

conclusionsA novel miRNA classification model using the identified prognostic and tumor stage associated miRNA signature will be useful for risk and stage stratification for clinical practice, and the identified miRNA signature can provide promising insight to understand the progression mechanism of ccRCC.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsMicroRNAsHumansNeoplasm StagingSurvival RateMicroRNAsBiomarkersClear cell renal cell carcinomaMachine learning classifiersMicroRNAsRegularized cox modelSurvival analysis

Identifiers

PMID34058987
PMCPMC8323484

What Socratic 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 Socratic graph.