Pancreatic ductal adenocarcinoma (PDAC) remains one of the most challenging cancers to treat, primarily due to its immunosuppressive tumor microenvironment and poor response to immune checkpoint inhibitors.1 Yes associated protein 1 (YAP1), a key effector of the Hippo pathway, regulates pivotal processes such as proliferation, survival, and differentiation in PDAC.2,3 Zinc-dependent regulation of zinc finger E-box-binding homeobox 1 (ZEB1), a transcription factor, has been shown to interact with YAP1, promoting epithelial-mesenchymal transition (EMT) plasticity and metastasis in PDAC.
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