The Hippo Pathway Effectors YAP/TAZ-TEAD Oncoproteins as Emerging Therapeutic Targets in the Tumor Microenvironment

Author:

Mokhtari Reza Bayat12,Ashayeri Neda3,Baghaie Leili2ORCID,Sambi Manpreet2,Satari Kosar3,Baluch Narges4,Bosykh Dmitriy A.1,Szewczuk Myron R.2ORCID,Chakraborty Sayan1ORCID

Affiliation:

1. Department of Pharmacology and Therapeutics, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263, USA

2. Department of Biomedical and Molecular Sciences, Queen’s University, Kingston, ON K7L 3N6, Canada

3. Division of Hematology and Oncology, Department of Pediatrics, Ali-Asghar Children Hospital, Iran University of Medical Science, Tehran 1449614535, Iran

4. Department of Immunology and Allergy, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada

Abstract

Various cancer cell-associated intrinsic and extrinsic inputs act on YAP/TAZ proteins to mediate the hyperactivation of the TEAD transcription factor-based transcriptome. This YAP/TAZ-TEAD activity can override the growth-limiting Hippo tumor-suppressor pathway that maintains normal tissue homeostasis. Herein, we provide an integrated summary of the contrasting roles of YAP/TAZ during normal tissue homeostasis versus tumor initiation and progression. In addition to upstream factors that regulate YAP/TAZ in the TME, critical insights on the emerging functions of YAP/TAZ in immune suppression and abnormal vasculature development during tumorigenesis are illustrated. Lastly, we discuss the current methods that intervene with the YAP/TAZ-TEAD oncogenic signaling pathway and the emerging applications of combination therapies, gut microbiota, and epigenetic plasticity that could potentiate the efficacy of chemo/immunotherapy as improved cancer therapeutic strategies.

Funder

CCSG grant of the Developmental Therapeutics Program at Roswell Park Cancer Institute

Department of Pharmacology and Therapeutics core funds

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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