Institut Català de la Salut
[Knapen DG, Hone Lopez S, de Groot DJA, de Haan JJ, de Vries EGE] Department of Medical Oncology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands. [Dienstmann R] Oncology Data Science (ODysSey) Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
Vall d'Hebron Barcelona Hospital Campus
2024-05-09T07:37:35Z
2024-05-09T07:37:35Z
2024-05-03
Patrons transcripcionals; Supervivència; Càncer colorectal precoz
Transcriptional patterns; Survival; Early Colorectal cancer
Patrones transcripcionales; Supervivencia; Cáncer colorrectal precoç
Background Bulk transcriptional profiles of early colorectal cancer (CRC) can fail to detect biological processes associated with disease-free survival (DFS) if the transcriptional patterns are subtle and/or obscured by other processes’ patterns. Consensus-independent component analysis (c-ICA) can dissect such transcriptomes into statistically independent transcriptional components (TCs), capturing both pronounced and subtle biological processes. Methods In this study we (1) integrated transcriptomes (n = 4228) from multiple early CRC studies, (2) performed c-ICA to define the TC landscape within this integrated data set, 3) determined the biological processes captured by these TCs, (4) performed Cox regression to identify DFS-associated TCs, (5) performed random survival forest (RSF) analyses with activity of DFS-associated TCs as classifiers to identify subgroups of patients, and 6) performed a sensitivity analysis to determine the robustness of our results Results We identify 191 TCs, 43 of which are associated with DFS, revealing transcriptional diversity among DFS-associated biological processes. A prominent example is the epithelial-mesenchymal transition (EMT), for which we identify an association with nine independent DFS-associated TCs, each with coordinated upregulation or downregulation of various sets of genes. Conclusions This finding indicates that early CRC may have nine distinct routes to achieve EMT, each requiring a specific peri-operative treatment strategy. Finally, we stratify patients into DFS patient subgroups with distinct transcriptional patterns associated with stage 2 and stage 3 CRC.
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Anglès
Recte - Càncer - Tractament; Còlon - Càncer - Tractament; Expressió gènica; Càncer - Recaiguda; DISEASES::Neoplasms::Neoplasms by Site::Digestive System Neoplasms::Gastrointestinal Neoplasms::Intestinal Neoplasms::Colorectal Neoplasms; Other subheadings::Other subheadings::/therapy; ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Investigative Techniques::Genetic Techniques::Gene Expression Profiling; DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Recurrence, Local; ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias del sistema digestivo::neoplasias gastrointestinales::neoplasias intestinales::neoplasias colorrectales; Otros calificadores::Otros calificadores::/terapia; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::técnicas de investigación::técnicas genéticas::perfiles de expresión génica; ENFERMEDADES::neoplasias::procesos neoplásicos::recurrencia neoplásica local
Nature Portfolio
Communications Medicine;4
https://doi.org/10.1038/s43856-024-00504-z
Attribution 4.0 International
http://creativecommons.org/licenses/by/4.0/