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

被引:6
|
作者
Liu, Chang [1 ]
Song, Yang [2 ]
Li, DeMing [3 ]
Wang, Biao [4 ]
机构
[1] China Med Univ, Dept Radiat Oncol, Hosp 1, Shenyang, Liaoning Provin, Peoples R China
[2] Fourth Peoples Hosp Shenyang, Geriatr Ctr, Shenyang, Liaoning Provin, Peoples R China
[3] China Med Univ, Dept Anesthesiol, Affiliated Hosp 4, Shenyang, Liaoning Provin, Peoples R China
[4] China Med Univ, Dept Biochem & Mol Biol, Sch Life Sci, Shenyang, Liaoning Provin, Peoples R China
关键词
Hippo pathway; Tumor immune microenvironments; Immunotherapy; CELLS; RECEPTOR; DIFFERENTIATION;
D O I
10.1016/j.intimp.2023.110586
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页数:7
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