Transcriptional co-activators YAP/TAZ: Potential therapeutic targets for metastatic breast cancer
Wenxia Zhao1, Mengyan Wang1, Meilian Cai1
1NHC Key Laboratory of Antibiotic Bioengineering, Laboratory of Oncology, Institute of Medicinal Biotechnology, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, 100050, China.
Abstract:
Breast cancer is the most commonly diagnosed cancer among women. Although routine and targeted therapies have improved the survival rate, there are still considerable challenges in the treatment of breast cancer. Metastasis is the leading cause of death in patients diagnosed with breast cancer. Yes-associated protein (YAP) and/or PDZ binding motif (TAZ) are usually abnormally activated in breast cancer leading to a variety of effects on tumour promotion, such as epithelial-mesenchymal transition, cancer stem cell production and drug-resistance. The abnormal activation of YAP/TAZ can affect metastasis-related processes and promote cancer progression and metastasis by interacting with some metastasis-related factors and pathways. In this article, we summarise the evidence that YAP/TAZ regulates breast cancer metastasis, its post-translational modification mechanisms, and the latest advances in the treatment of YAP/TAZ-related breast cancer metastasis, besides providing a new strategy of YAP/TAZ-based treatment of human breast cancer.
Insights
Yes-associated protein (YAP) and/or PDZ binding motif (TAZ) activation drives breast cancer metastasis. Targeting YAP/TAZ offers a promising new strategy for treating advanced breast cancer and improving patient survival rates.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Breast cancer remains a leading cause of cancer-related death in women worldwide.
- Metastasis is the primary driver of mortality in breast cancer patients.
- Abnormal activation of Yes-associated protein (YAP) and PDZ binding motif (TAZ) pathways is implicated in tumor progression.
Purpose of the Study:
- To review the role of YAP/TAZ in regulating breast cancer metastasis.
- To summarize YAP/TAZ post-translational modification mechanisms.
- To discuss novel therapeutic strategies targeting YAP/TAZ for breast cancer treatment.
Main Methods:
- Literature review of studies investigating YAP/TAZ in breast cancer.
- Analysis of molecular mechanisms linking YAP/TAZ to metastasis.
- Evaluation of current and emerging therapeutic approaches targeting YAP/TAZ.
Main Results:
- YAP/TAZ activation promotes key metastatic processes including epithelial-mesenchymal transition, cancer stem cell generation, and drug resistance.
- YAP/TAZ interacts with metastasis-related factors and pathways, driving cancer progression.
- Evidence supports YAP/TAZ as a critical regulator of breast cancer metastasis.
Conclusions:
- YAP/TAZ signaling is a significant contributor to breast cancer metastasis.
- Targeting YAP/TAZ and its regulatory pathways presents a promising therapeutic avenue.
- Further research into YAP/TAZ-based treatments could improve outcomes for breast cancer patients.
More Related Videos
11:32Identification of Transcription Factor Regulators using Medium-Throughput Screening of Arrayed Libraries and a Dual-Luciferase-Based Reporter
Published on: March 27, 2020
03:37Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
Published on: March 1, 2024
Related Concept Videos
Co-activators and Co-repressors
Co-activators and Co-repressors
Master Transcription Regulators
Master Transcription Regulators
Targeted Cancer Therapies
There are several types of targeted therapies against...
Eukaryotic Transcription Activators
The binding domains are capable of recognizing and interacting with regulatory sequences on the DNA. These...
