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Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer

Non-small Cell Lung Cancer (NSCLC) is a heterogeneous disease with a poor prognosis. Identifying novel subtypes in cancer can help classify patients with similar molecular and clinical phenotypes. This work proposes an end-to-end pipeline for subgroup identification in NSCLC. Here, we used a machine...

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Autores principales: Khadirnaikar, Seema, Shukla, Sudhanshu, Prasanna, S. R. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030850/
https://www.ncbi.nlm.nih.gov/pubmed/36944673
http://dx.doi.org/10.1038/s41598-023-31426-w
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author Khadirnaikar, Seema
Shukla, Sudhanshu
Prasanna, S. R. M.
author_facet Khadirnaikar, Seema
Shukla, Sudhanshu
Prasanna, S. R. M.
author_sort Khadirnaikar, Seema
collection PubMed
description Non-small Cell Lung Cancer (NSCLC) is a heterogeneous disease with a poor prognosis. Identifying novel subtypes in cancer can help classify patients with similar molecular and clinical phenotypes. This work proposes an end-to-end pipeline for subgroup identification in NSCLC. Here, we used a machine learning (ML) based approach to compress the multi-omics NSCLC data to a lower dimensional space. This data is subjected to consensus K-means clustering to identify the five novel clusters (C1–C5). Survival analysis of the resulting clusters revealed a significant difference in the overall survival of clusters (p-value: 0.019). Each cluster was then molecularly characterized to identify specific molecular characteristics. We found that cluster C3 showed minimal genetic aberration with a high prognosis. Next, classification models were developed using data from each omic level to predict the subgroup of unseen patients. Decision‑level fused classification models were then built using these classifiers, which were used to classify unseen patients into five novel clusters. We also showed that the multi-omics-based classification model outperformed single-omic-based models, and the combination of classifiers proved to be a more accurate prediction model than the individual classifiers. In summary, we have used ML models to develop a classification method and identified five novel NSCLC clusters with different genetic and clinical characteristics.
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spelling pubmed-100308502023-03-23 Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer Khadirnaikar, Seema Shukla, Sudhanshu Prasanna, S. R. M. Sci Rep Article Non-small Cell Lung Cancer (NSCLC) is a heterogeneous disease with a poor prognosis. Identifying novel subtypes in cancer can help classify patients with similar molecular and clinical phenotypes. This work proposes an end-to-end pipeline for subgroup identification in NSCLC. Here, we used a machine learning (ML) based approach to compress the multi-omics NSCLC data to a lower dimensional space. This data is subjected to consensus K-means clustering to identify the five novel clusters (C1–C5). Survival analysis of the resulting clusters revealed a significant difference in the overall survival of clusters (p-value: 0.019). Each cluster was then molecularly characterized to identify specific molecular characteristics. We found that cluster C3 showed minimal genetic aberration with a high prognosis. Next, classification models were developed using data from each omic level to predict the subgroup of unseen patients. Decision‑level fused classification models were then built using these classifiers, which were used to classify unseen patients into five novel clusters. We also showed that the multi-omics-based classification model outperformed single-omic-based models, and the combination of classifiers proved to be a more accurate prediction model than the individual classifiers. In summary, we have used ML models to develop a classification method and identified five novel NSCLC clusters with different genetic and clinical characteristics. Nature Publishing Group UK 2023-03-21 /pmc/articles/PMC10030850/ /pubmed/36944673 http://dx.doi.org/10.1038/s41598-023-31426-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Khadirnaikar, Seema
Shukla, Sudhanshu
Prasanna, S. R. M.
Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer
title Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer
title_full Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer
title_fullStr Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer
title_full_unstemmed Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer
title_short Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer
title_sort machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030850/
https://www.ncbi.nlm.nih.gov/pubmed/36944673
http://dx.doi.org/10.1038/s41598-023-31426-w
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