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Updated: Oct 13, 2025

Identification of Transcription Factor Regulators using Medium-Throughput Screening of Arrayed Libraries and a Dual-Luciferase-Based Reporter
Published on: March 27, 2020
Mechanisms of YAP/TAZ transcriptional control
Giusy Battilana1, Francesca Zanconato1, Stefano Piccolo1,2
1Department of Molecular Medicine, University of Padua, Via G. Colombo 3, 35131, Padua, Italy.
Abstract:
Dysregulated gene expression is intrinsic to cell transformation, tumorigenesis and metastasis. Cancer-specific gene-expression profiles stem from gene regulatory networks fueled by genetic and epigenetic defects, and by abnormal signals of the tumor microenvironment. These oncogenic signals ultimately engage the transcriptional machinery on the cis -regulatory elements of a host of effector genes, through recruitment of transcription factors (TFs), co-activators and chromatin regulators. That said, whether gene-expression in cancer cells is the chaotic product of myriad regulations or rather a relatively ordered process orchestrated by few TFs (master regulators) has long remained enigmatic. Recent work on the YAP/TAZ co-activators has been instrumental to break new ground into this outstanding issue, revealing that tumor cells hijack growth programs that are active during development and regeneration through engagement of a small set of interconnected TFs and their nuclear partners.
Insights
Cancer cells hijack developmental gene programs using a few key transcription factors (TFs) and co-activators like YAP/TAZ. This reveals an ordered process, not chaos, in cancer gene expression.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Dysregulated gene expression drives cancer development, including cell transformation, tumorigenesis, and metastasis.
- Cancer gene expression arises from complex networks influenced by genetic/epigenetic changes and the tumor microenvironment.
- The precise orchestration of cancer gene expression—whether chaotic or ordered by master regulators—remains an open question.
Purpose of the Study:
- To investigate whether cancer gene expression is a chaotic outcome or an ordered process controlled by a few key transcription factors (TFs).
- To elucidate the role of YAP/TAZ co-activators in mediating gene expression changes in cancer cells.
Main Methods:
- Analysis of gene regulatory networks in cancer cells.
- Investigating the function of YAP/TAZ co-activators and their associated transcription factors.
- Studying the engagement of transcriptional machinery at cis-regulatory elements.
Main Results:
- Recent research highlights YAP/TAZ co-activators as crucial players in cancer gene regulation.
- Tumor cells utilize developmental and regenerative growth programs by engaging specific sets of interconnected TFs and nuclear partners.
- This suggests an ordered regulatory mechanism rather than a purely chaotic one.
Conclusions:
- Cancer cells co-opt conserved cellular programs through a limited set of master regulators, including YAP/TAZ.
- This provides insight into the ordered nature of oncogenic gene expression.
- Understanding these master regulators offers potential therapeutic targets for cancer treatment.
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