| Literature DB >> 29329638 |
Miho Akimoto1, Keizo Takenaga2.
Abstract
Interleukin-33 (IL-33) has been identified as a natural ligand of ST2L. IL-33 primarily acts as a key regulator of Th2 responses through binding to ST2L, which is antagonized by soluble ST2 (sST2). The IL-33/ST2L axis is involved in various inflammatory pathologies, including ulcerative colitis (UC). Several recent investigations have also suggested that the IL-33/ST2L axis plays a role in colorectal cancer (CRC) progression. In CRC, tumor- and stroma-derived IL-33 may activate ST2L on various cell types in an autocrine and paracrine manner. Although several findings support the hypothesis that the IL-33/ST2L axis positively regulates CRC progression, other reports do not; hence, this hypothesis remains controversial. At any rate, recent studies have provided overwhelming evidence that the IL-33/ST2L axis plays important roles in CRC progression. This review summarizes the role of the IL-33/ST2L axis in the UC and CRC microenvironments.Entities:
Keywords: Colorectal cancer; Inflammatory tumor microenvironment; Interleukin-33; ST2L; Ulcerative colitis; sST2
Mesh:
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Year: 2018 PMID: 29329638 DOI: 10.1016/j.cellimm.2017.12.014
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868