The emerging roles of Hedgehog signaling in tumor immune microenvironment

The Hedgehog (Hh) signaling pathway is pervasively involved in human malignancies, making it an effective target for cancer treatment for decades. In addition to its direct role in regulating cancer cell attributes, recent work indicates that it has an immunoregulatory effect on tumor microenvironme...

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Published inFrontiers in oncology Vol. 13; p. 1171418
Main Authors Wang, Juan, Cui, Baiping, Li, Xiaojie, Zhao, Xinyue, Huang, Taomin, Ding, Xiaolei
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 05.05.2023
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Summary:The Hedgehog (Hh) signaling pathway is pervasively involved in human malignancies, making it an effective target for cancer treatment for decades. In addition to its direct role in regulating cancer cell attributes, recent work indicates that it has an immunoregulatory effect on tumor microenvironments. An integrated understanding of these actions of Hh signaling pathway in tumor cells and tumor microenvironments will pave the way for novel tumor treatments and further advances in anti-tumor immunotherapy. In this review, we discuss the most recent research about Hh signaling pathway transduction, with a particular emphasis on its role in modulating tumor immune/stroma cell phenotype and function, such as macrophage polarity, T cell response, and fibroblast activation, as well as their mutual interactions between tumor cells and nonneoplastic cells. We also summarize the recent advances in the development of Hh pathway inhibitors and nanoparticle formulation for Hh pathway modulation. We suggest that targeting Hh signaling effects on both tumor cells and tumor immune microenvironments could be more synergistic for cancer treatment.
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These authors have contributed equally to this work
Reviewed by: James Kim, University of Texas Southwestern Medical Center, United States; Lucia Di Marcotullio, Sapienza University of Rome, Italy
Edited by: Keqiang Zhang, City of Hope National Medical Center, United States
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2023.1171418