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Updated: Jun 15, 2026

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Published on: July 3, 2025
A novel meta-analysis approach of cancer transcriptomes reveals prevailing transcriptional networks in cancer cells
Atsushi Niida1, Seiya Imoto, Masao Nagasaki
1Human Genome Center, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan. aniida@ims.u-tokyo.ac.jp
Abstract:
Although microarray technology has revealed transcriptomic diversities underlining various cancer phenotypes, transcriptional programs controlling them have not been well elucidated. To decode transcriptional programs governing cancer transcriptomes, we have recently developed a computational method termed EEM, which searches for expression modules from prescribed gene sets defined by prior biological knowledge like TF binding motifs. In this paper, we extend our EEM approach to predict cancer transcriptional networks. Starting from functional TF binding motifs and expression modules identified by EEM, we predict cancer transcriptional networks containing regulatory TFs, associated GO terms, and interactions between TF binding motifs. To systematically analyze transcriptional programs in broad types of cancer, we applied our EEM-based network prediction method to 122 microarray datasets collected from public databases. The data sets contain about 15000 experiments for tumor samples of various tissue origins including breast, colon, lung etc. This EEM based meta-analysis successfully revealed a prevailing cancer transcriptional network which functions in a large fraction of cancer transcriptomes; they include cell-cycle and immune related sub-networks. This study demonstrates broad applicability of EEM, and opens a way to comprehensive understanding of transcriptional networks in cancer cells.
Insights
We developed a computational method, Expression Exploration Modules (EEM), to predict cancer transcriptional networks. This approach reveals a common cancer network involving cell-cycle and immune functions across diverse tumor types.
Area of Science:
- Computational Biology
- Cancer Genomics
- Systems Biology
Background:
- Microarray technology has identified transcriptomic variations in cancer.
- Transcriptional programs driving these variations remain poorly understood.
- Existing methods lack comprehensive analysis of cancer transcriptomes.
Purpose of the Study:
- To develop and apply a computational method for predicting cancer transcriptional networks.
- To elucidate the regulatory mechanisms underlying cancer phenotypes.
- To identify common transcriptional programs across various cancer types.
Main Methods:
- Extended the Expression Exploration Modules (EEM) computational method.
- EEM identifies expression modules from gene sets based on biological knowledge (e.g., TF binding motifs).
- Applied EEM to 122 public microarray datasets (approx. 15,000 experiments) from diverse cancer tissues.
Main Results:
- Successfully predicted cancer transcriptional networks.
- Identified a prevailing cancer transcriptional network present in a large fraction of transcriptomes.
- Discovered cell-cycle and immune-related sub-networks within the prevailing network.
Conclusions:
- The EEM approach is broadly applicable for predicting cancer transcriptional networks.
- This study provides a comprehensive understanding of transcriptional regulation in cancer.
- Opens new avenues for investigating cancer biology through network analysis.
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