Evidence map›Paper›PMID 37958210›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Cancer Metastasis Prediction and Genomic Biomarker Identification through Machine Learning and eXplainable Artificial Intelligence in Breast Cancer Research.

Burak Yagin, Fatma Hilal Yagin, Cemil Colak, Feyza Inceoglu, Seifedine Kadry, Jungeun Kim

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

26 citing papers in PubMed, 48 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

6 authors at 4 institutions in 4 countries.

Burak YaginDepartment of Biostatistics and Medical Informatics, Faculty of Medicine, Inonu University, Malatya 44280, Turkey.ORCID 0000-0001-6687-979X
Fatma Hilal YaginDepartment of Biostatistics and Medical Informatics, Faculty of Medicine, Inonu University, Malatya 44280, Turkey.ORCID 0000-0002-9848-7958
Cemil ColakDepartment of Biostatistics and Medical Informatics, Faculty of Medicine, Inonu University, Malatya 44280, Turkey.ORCID 0000-0001-5406-098X
Feyza InceogluDepartment of Biostatistics, Faculty of Medicine, Malatya Turgut Ozal University, Malatya 44090, Turkey.
Seifedine KadryDepartment of applied Data science, Noroff University College, 4612 Kristiansand, Norway.ORCID 0000-0002-1939-4842
Jungeun KimDepartment of Software, Kongju National University, Cheonan 31080, Republic of Korea.
Inonu University · TRAjman University · AEKongju National University · KRTurgut Özal University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimMethod: This research presents a model combining machine learning (ML) techniques and eXplainable artificial intelligence (XAI) to predict breast cancer (BC) metastasis and reveal important genomic biomarkers in metastasis patients.

methodA total of 98 primary BC samples was analyzed, comprising 34 samples from patients who developed distant metastases within a 5-year follow-up period and 44 samples from patients who remained disease-free for at least 5 years after diagnosis. Genomic data were then subjected to biostatistical analysis, followed by the application of the elastic net feature selection method. This technique identified a restricted number of genomic biomarkers associated with BC metastasis. A light gradient boosting machine (LightGBM), categorical boosting (CatBoost), Extreme Gradient Boosting (XGBoost), Gradient Boosting Trees (GBT), and Ada boosting (AdaBoost) algorithms were utilized for prediction. To assess the models' predictive abilities, the accuracy, F1 score, precision, recall, area under the ROC curve (AUC), and Brier score were calculated as performance evaluation metrics. To promote interpretability and overcome the "black box" problem of ML models, a SHapley Additive exPlanations (SHAP) method was employed.

resultsThe LightGBM model outperformed other models, yielding remarkable accuracy of 96% and an AUC of 99.3%. In addition to biostatistical evaluation, in XAI-based SHAP results, increased expression levels of TSPYL5, ATP5E, CA9, NUP210, SLC37A1, ARIH1, PSMD7, UBQLN1, PRAME, and UBE2T (

conclusionThe findings of this study may prevent disease progression and metastases and potentially improve clinical outcomes by recommending customized treatment approaches for BC patients.

Indexed as

breast cancer metastasiseXplainable artificial intelligencegenomic biomarkersmachine learning algorithmsSHAP

Identifiers

PMID37958210
PMCPMC10650093
OpenAlexW4387959306

What Socratic 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 Socratic graph.