Abstract

BackgroundCancer is a complex disease driven by somatic genomic alterations (SGAs) that perturb signaling pathways and consequently cellular function. Identifying patterns of pathway perturbations would provide insights into common disease mechanisms shared among tumors, which is important for guiding treatment and predicting outcome. However, identifying perturbed pathways is challenging, because different tumors can have the same perturbed pathways that are perturbed by different SGAs. Here, we designed novel semantic representations that capture the functional similarity of distinct SGAs perturbing a common pathway in different tumors. Combining this representation with topic modeling would allow us to identify patterns in altered signaling pathways.ResultsWe represented each gene with a vector of words describing its function, and we represented the SGAs of a tumor as a text document by pooling the words representing individual SGAs. We applied the nested hierarchical Dirichlet process (nHDP) model to a collection of tumors of 5 cancer types from TCGA. We identified topics (consisting of co-occurring words) representing the common functional themes of different SGAs. Tumors were clustered based on their topic associations, such that each cluster consists of tumors sharing common functional themes. The resulting clusters contained mixtures of cancer types, which indicates that different cancer types can share disease mechanisms. Survival analysis based on the clusters revealed significant differences in survival among the tumors of the same cancer type that were assigned to different clusters.ConclusionsThe results indicate that applying topic modeling to semantic representations of tumors identifies patterns in the combinations of altered functional pathways in cancer.

Highlights

  • Cancer is a complex disease driven by somatic genomic alterations (SGAs) that perturb signaling pathways and cellular function

  • The Author(s) BMC Genomics 2017, 18(Suppl 2):105 causative pathways underlying the development of subtypes. As such, such subtyping does not provide guidance for targeted therapy. Another limitation of transcriptomics-based subtyping is that tissue-specific gene expression prevents discovery of transcriptomic patterns across cancer types

  • Recent pan-cancer studies found that tumors are invariably clustered according to tissue of origins when using features that are related to transcriptomics [12, 13]

Read more

Summary

Introduction

Cancer is a complex disease driven by somatic genomic alterations (SGAs) that perturb signaling pathways and cellular function. Identifying patterns of pathway perturbations would provide insights into common disease mechanisms shared among tumors, which is important for guiding treatment and predicting outcome. We designed novel semantic representations that capture the functional similarity of distinct SGAs perturbing a common pathway in different tumors Combining this representation with topic modeling would allow us to identify patterns in altered signaling pathways. Identification of patterns of pathway perturbations can reveal common disease mechanisms shared by a tumor subtype and such information can guide targeted therapy. The Author(s) BMC Genomics 2017, 18(Suppl 2):105 causative pathways underlying the development of subtypes As such, such subtyping does not provide guidance for targeted therapy. Studying common disease mechanism of cancers should be addressed from new perspectives

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.