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Risk Stratification for Breast Cancer Patient by Simultaneous Learning of Molecular Subtype and Survival Outcome Using Genetic Algorithm-Based Gene Set Selection.
Koo, Bonil; Lee, Dohoon; Lee, Sangseon; Sung, Inyoung; Kim, Sun; Lee, Sunho.
Afiliación
  • Koo B; Interdisciplinary Program in Bioinformatics, Seoul National University, Seoul 08826, Korea.
  • Lee D; Bioinformatics Institute, Seoul National University, Seoul 08826, Korea.
  • Lee S; BK21 FOUR Intelligence Computing, Seoul National University, Seoul 08826, Korea.
  • Sung I; Institute of Computer Technology, Seoul National University, Seoul 08826, Korea.
  • Kim S; Interdisciplinary Program in Bioinformatics, Seoul National University, Seoul 08826, Korea.
  • Lee S; Interdisciplinary Program in Bioinformatics, Seoul National University, Seoul 08826, Korea.
Cancers (Basel) ; 14(17)2022 Aug 25.
Article en En | MEDLINE | ID: mdl-36077657
Patient stratification is a clinically important task because it allows us to establish and develop efficient treatment strategies for particular groups of patients. Molecular subtypes have been successfully defined using transcriptomic profiles, and they are used effectively in clinical practice, e.g., PAM50 subtypes of breast cancer. Survival prediction contributed to understanding diseases and also identifying genes related to prognosis. It is desirable to stratify patients considering these two aspects simultaneously. However, there are no methods for patient stratification that consider molecular subtypes and survival outcomes at once. Here, we propose a methodology to deal with the problem. A genetic algorithm is used to select a gene set from transcriptome data, and their expression quantities are utilized to assign a risk score to each patient. The patients are ordered and stratified according to the score. A gene set was selected by our method on a breast cancer cohort (TCGA-BRCA), and we examined its clinical utility using an independent cohort (SCAN-B). In this experiment, our method was successful in stratifying patients with respect to both molecular subtype and survival outcome. We demonstrated that the orders of patients were consistent across repeated experiments, and prognostic genes were successfully nominated. Additionally, it was observed that the risk score can be used to evaluate the molecular aggressiveness of individual patients.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Año: 2022 Tipo del documento: Article