Skip to content
Review Open access

The Crosstalk Between YAP/TAZ and Cancer Metabolism: From Mechanistic Insights to Drug Discovery

Aug 2026 · International Journal of Molecular Sciences · Vol 27, pp. 7537 · 0 citations · 134 references
Medicine

TL;DR

The interplay between YAP/TAZ and metabolic reprogramming in cancer is systematically clarified, the core molecular networks through which YAP/TAZ govern each metabolic pathway are delineated, and the current pharmacological inhibitors targeting YAP/TAZ-regulated metabolic networks are summarized.

Abstract

As the core transcriptional co-activators of the Hippo signaling pathway, YAP and TAZ play essential roles in maintaining tissue homeostasis and in tumorigenesis. Their aberrant activation is frequently observed in human malignancies, and accumulating evidence has identified them as crucial drivers of tumor initiation and progression. YAP/TAZ have been recently recognized as key regulators of cellular metabolic reprogramming, a hallmark of cancer that fuels tumor cell proliferation by rewiring glucose, lipid, amino acid, and nucleotide metabolism. Conversely, the activity of YAP/TAZ is modulated by metabolites such as glucose and lipids, establishing a complex bidirectional regulatory circuit. Therefore, deciphering this intricate crosstalk is of great importance for cancer therapy and drug discovery. In this review, we systematically clarify the interplay between YAP/TAZ and metabolic reprogramming in cancer, delineate the core molecular networks through which YAP/TAZ govern each metabolic pathway, and summarize the current pharmacological inhibitors targeting YAP/TAZ-regulated metabolic networks. Collectively, these findings pave the way for therapeutic approaches targeting YAP/TAZ-driven metabolic vulnerabilities in cancer.

Read PDF

Similar papers

Review Open access Sep 2026

Hippo Pathway–YAP/TAZ Signaling: Molecular Mechanisms, Biological Function, Diseases, and Therapeutic Targets

ABSTRACT The Hippo pathway and its downstream effectors Yes‐associated protein/transcriptional coactivator with PDZ‐binding motif‐TEA domain transcription factor (YAP/TAZ–TEAD) play critical roles in organ‐size control, tissue homeostasis, regeneration, and stem‐cell biology. Their aberrant activation drives malignanci...

Xiao-Dan Qu, Zhan-You Wang · 0 citations
Review Aug 2026

Transcriptional and Epigenetic Regulation of Cell Fate by YAP and TAZ.

Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) (YAP/TAZ) are key transcriptional coregulators that govern mammalian cell fate through complex epigenetic mechanisms. As core effectors of the Hippo signaling pathway, they integrate diverse cellular signals-including those mechan...

Ju-Gyeong Kang, Taejun Seol, Younghoon Kim et al. · 0 citations
Review Open access Sep 2026

Molecular Signaling Pathways, Regulatory and Coactivator Networks, and Emerging Mechanisms in Hepatocellular Carcinoma

Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and a leading cause of cancer-related mortality worldwide. Despite advances in diagnosis and therapy, the prognosis for advanced HCC remains poor due to late-stage diagnosis, high recurrence rates, therapeutic resistance, and pronounced molecula...

R. Srivastava, Pratibha Singh, D. Lonard · 0 citations
Review Aug 2026

Hippo-YAP/TAZ Signaling in the Respiratory System.

The Hippo signaling pathway and its effectors Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) have emerged as central regulators of respiratory biology, playing essential functions in the development, homeostasis, and regeneration of the lung and trachea. Here, we review the sp...

K. Kontodimas, X. Varelas · 0 citations
Review Aug 2026

MicroRNAs and Their Crosstalk with Oncogenic Pathways in Gastric Cancer.

Gastric Cancer (GC) is the fifth most frequently diagnosed malignancy and the third leading cause of cancer-related mortality worldwide. The aggressive nature of GC, coupled with late clinical presentation and limited therapeutic options, underscores the urgent need for a deeper molecular understanding of its pathogene...

Liu-Shan Wei, Jia Yu, Yan Hu et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.