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Monitoring Hippo Signaling Pathway Activity Using a Luciferase-based Large Tumor Suppressor LATS Biosensor
Published on: September 13, 2018
Reconstruction of the genome-scale co-expression network for the Hippo signaling pathway in colorectal cancer
Fariba Dehghanian1, Zohreh Hojati1, Nazanin Hosseinkhan2
1Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, P.O. Box 81746-73441, Isfahan, Iran.
Abstract:
The Hippo signaling pathway (HSP) has been identified as an essential and complex signaling pathway for tumor suppression that coordinates proliferation, differentiation, cell death, cell growth and stemness. In the present study, we conducted a genome-scale co-expression analysis to reconstruct the HSP in colorectal cancer (CRC). Five key modules were detected through network clustering, and a detailed discussion of two modules containing respectively 18 and 13 over and down-regulated members of HSP was provided. Our results suggest new potential regulatory factors in the HSP. The detected modules also suggest novel genes contributing to CRC. Moreover, differential expression analysis confirmed the differential expression pattern of HSP members and new suggested regulatory factors between tumor and normal samples. These findings can further reveal the importance of HSP in CRC.
Insights
The Hippo signaling pathway (HSP) is crucial for tumor suppression. This study reconstructs HSP in colorectal cancer (CRC), identifying key modules and potential regulatory factors that could offer new therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- The Hippo signaling pathway (HSP) plays a vital role in tumor suppression.
- HSP regulates critical cellular processes including proliferation, differentiation, apoptosis, and stemness.
- Dysregulation of HSP is implicated in various cancers, including colorectal cancer (CRC).
Purpose of the Study:
- To reconstruct the Hippo signaling pathway (HSP) in colorectal cancer (CRC) using genome-scale co-expression analysis.
- To identify key regulatory modules and potential novel genes within the HSP in CRC.
- To investigate the differential expression patterns of HSP members and regulatory factors in CRC tumors versus normal samples.
Main Methods:
- Genome-scale co-expression network analysis was employed to reconstruct the HSP.
- Network clustering techniques were utilized to detect key functional modules within the pathway.
- Differential expression analysis was performed to compare gene expression between tumor and normal tissues.
Main Results:
- Five key modules within the HSP in CRC were identified through network clustering.
- Two specific modules, comprising 18 and 13 differentially expressed HSP members (up- and down-regulated, respectively), were detailed.
- The analysis revealed novel potential regulatory factors and genes associated with CRC development.
- Differential expression analysis confirmed significant alterations in HSP members and identified new regulatory candidates in CRC samples.
Conclusions:
- The study provides a comprehensive reconstruction of the HSP in CRC, highlighting its complexity.
- Identified modules and regulatory factors offer potential new targets for CRC diagnosis and therapy.
- These findings underscore the critical importance of the Hippo signaling pathway in the pathogenesis of colorectal cancer.
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