Regulation of the tumor immune microenvironment by the Hippo Pathway: Implications for cancer immunotherapy

The tumor immune microenvironment (TIME) is a dynamic and complex ecosystem consisting of immune cells, stromal cells, and tumor cells. It plays a crucial role in shaping cancer progression and treatment outcomes. Notably, tumor-associated immune cells are key regulators within the TIME, influencing immune responses and therapeutic efficacy. The Hippo pathway is a critical signaling pathway involved in the TIME and cancer progression. In this review, we provide an overview of the Hippo pathway's role in the TIME, focusing on its interactions with immune cells and their implications in cancer biology and therapy. Specifically, we discuss the involvement of the Hippo pathway in regulating T-cell function, macrophage polarization, B-cell differentiation, MDSC activity, and dendritic cell-mediated immune responses. Furthermore, we explore its influence on PD-L1 expression in lymphocytes and its potential as a therapeutic target. While recent progress has been made in understanding the Hippo pathway's molecular mechanisms, challenges remain in deciphering its contextdependent effects in different cancers and identifying predictive biomarkers for targeted therapies. By elucidating the intricate crosstalk between the Hippo pathway and the TME, we aim to contribute to the development of innovative strategies for cancer treatment.

Automated summary

The tumor immune microenvironment (TIME) consists of immune cells, stromal cells, and tumor cells, and plays a crucial role in cancer progression and treatment outcomes. The Hippo pathway, a critical signaling pathway, has interactions with immune cells in the TIME, influencing cancer biology and therapy. Understanding the role of the Hippo pathway in immune responses and its potential as a therapeutic target can contribute to innovative cancer treatment strategies.