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.

Cell Stress
|November 16, 2021
PubMed

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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