SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancer

Abstract Background Clear cell renal cell carcinoma (ccRCC) tumours develop and progress via complex remodelling of the kidney epigenome, transcriptome, proteome and metabolome. Given the subsequent tumour and inter-patient heterogeneity, drug-based treatments report limited success, calling for mul...

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Main Authors: Ariane Mora, Christina Schmidt, Brad Balderson, Christian Frezza, Mikael Bodén
Format: Article
Language:English
Published: BMC 2024-12-01
Series:Genome Medicine
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Online Access:https://doi.org/10.1186/s13073-024-01415-3
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author Ariane Mora
Christina Schmidt
Brad Balderson
Christian Frezza
Mikael Bodén
author_facet Ariane Mora
Christina Schmidt
Brad Balderson
Christian Frezza
Mikael Bodén
author_sort Ariane Mora
collection DOAJ
description Abstract Background Clear cell renal cell carcinoma (ccRCC) tumours develop and progress via complex remodelling of the kidney epigenome, transcriptome, proteome and metabolome. Given the subsequent tumour and inter-patient heterogeneity, drug-based treatments report limited success, calling for multi-omics studies to extract regulatory relationships, and ultimately, to develop targeted therapies. Yet, methods for multi-omics integration to reveal mechanisms of phenotype regulation are lacking. Methods Here, we present SiRCle (Signature Regulatory Clustering), a method to integrate DNA methylation, RNA-seq and proteomics data at the gene level by following central dogma of biology, i.e. genetic information proceeds from DNA, to RNA, to protein. To identify regulatory clusters across the different omics layers, we group genes based on the layer where the gene’s dysregulation first occurred. We combine the SiRCle clusters with a variational autoencoder (VAE) to reveal key features from omics’ data for each SiRCle cluster and compare patient subpopulations in a ccRCC and a PanCan cohort. Results Applying SiRCle to a ccRCC cohort, we showed that glycolysis is upregulated by DNA hypomethylation, whilst mitochondrial enzymes and respiratory chain complexes are translationally suppressed. Additionally, we identify metabolic enzymes associated with survival along with the possible molecular driver behind the gene’s perturbations. By using the VAE to integrate omics’ data followed by statistical comparisons between tumour stages on the integrated space, we found a stage-dependent downregulation of proximal renal tubule genes, hinting at a loss of cellular identity in cancer cells. We also identified the regulatory layers responsible for their suppression. Lastly, we applied SiRCle to a PanCan cohort and found common signatures across ccRCC and PanCan in addition to the regulatory layer that defines tissue identity. Conclusions Our results highlight SiRCle’s ability to reveal mechanisms of phenotype regulation in cancer, both specifically in ccRCC and broadly in a PanCan context. SiRCle ranks genes according to biological features. https://github.com/ArianeMora/SiRCle_multiomics_integration .
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spelling doaj-art-c0ffeed62cb74c2e87e0394d0b82398f2025-08-20T02:20:45ZengBMCGenome Medicine1756-994X2024-12-0116112610.1186/s13073-024-01415-3SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancerAriane Mora0Christina Schmidt1Brad Balderson2Christian Frezza3Mikael Bodén4School of Chemistry and Molecular Biosciences, University of QueenslandMedical Research Council Cancer Unit, Hutchison/MRC Research Centre, University of CambridgeSchool of Chemistry and Molecular Biosciences, University of QueenslandUniversity of Cologne, Faculty of Medicine and University Hospital Cologne, Institute for Metabolomics in Ageing, Cluster of Excellence Cellular Stress Responses in Aging-associated Diseases (CECAD)School of Chemistry and Molecular Biosciences, University of QueenslandAbstract Background Clear cell renal cell carcinoma (ccRCC) tumours develop and progress via complex remodelling of the kidney epigenome, transcriptome, proteome and metabolome. Given the subsequent tumour and inter-patient heterogeneity, drug-based treatments report limited success, calling for multi-omics studies to extract regulatory relationships, and ultimately, to develop targeted therapies. Yet, methods for multi-omics integration to reveal mechanisms of phenotype regulation are lacking. Methods Here, we present SiRCle (Signature Regulatory Clustering), a method to integrate DNA methylation, RNA-seq and proteomics data at the gene level by following central dogma of biology, i.e. genetic information proceeds from DNA, to RNA, to protein. To identify regulatory clusters across the different omics layers, we group genes based on the layer where the gene’s dysregulation first occurred. We combine the SiRCle clusters with a variational autoencoder (VAE) to reveal key features from omics’ data for each SiRCle cluster and compare patient subpopulations in a ccRCC and a PanCan cohort. Results Applying SiRCle to a ccRCC cohort, we showed that glycolysis is upregulated by DNA hypomethylation, whilst mitochondrial enzymes and respiratory chain complexes are translationally suppressed. Additionally, we identify metabolic enzymes associated with survival along with the possible molecular driver behind the gene’s perturbations. By using the VAE to integrate omics’ data followed by statistical comparisons between tumour stages on the integrated space, we found a stage-dependent downregulation of proximal renal tubule genes, hinting at a loss of cellular identity in cancer cells. We also identified the regulatory layers responsible for their suppression. Lastly, we applied SiRCle to a PanCan cohort and found common signatures across ccRCC and PanCan in addition to the regulatory layer that defines tissue identity. Conclusions Our results highlight SiRCle’s ability to reveal mechanisms of phenotype regulation in cancer, both specifically in ccRCC and broadly in a PanCan context. SiRCle ranks genes according to biological features. https://github.com/ArianeMora/SiRCle_multiomics_integration .https://doi.org/10.1186/s13073-024-01415-3IntegrationMulti-omicsRegulationMachine learningVariational autoencoderClear cell renal cell carcinoma
spellingShingle Ariane Mora
Christina Schmidt
Brad Balderson
Christian Frezza
Mikael Bodén
SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancer
Genome Medicine
Integration
Multi-omics
Regulation
Machine learning
Variational autoencoder
Clear cell renal cell carcinoma
title SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancer
title_full SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancer
title_fullStr SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancer
title_full_unstemmed SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancer
title_short SiRCle (Signature Regulatory Clustering) model integration reveals mechanisms of phenotype regulation in renal cancer
title_sort sircle signature regulatory clustering model integration reveals mechanisms of phenotype regulation in renal cancer
topic Integration
Multi-omics
Regulation
Machine learning
Variational autoencoder
Clear cell renal cell carcinoma
url https://doi.org/10.1186/s13073-024-01415-3
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