| Literature DB >> 32355198 |
Hadas Shatz-Azoulay1, Yaron Vinik1, Roi Isaac1, Ulrike Kohler1, Sima Lev1, Yehiel Zick2.
Abstract
Secreted animal lectins of the galectin family are key players in cancer growth and metastasis. Here we show that galectin-8 (gal-8) induces the expression and secretion of cytokines and chemokines such as SDF-1 and MCP-1 in a number of cell types. This involves gal-8 binding to a uPAR/LRP1/integrin complex that activates JNK and the NFkB pathway. Cytokine and chemokine secretion, induced by gal-8, promotes migration of cancer cells toward cells treated with this lectin. Indeed, immune-competent gal-8 knockout (KO) mice express systemic lower levels of cytokines and chemokines while the opposite is true for gal-8 transgenic animals. Accordingly, gal-8 KO mice experience reduced tumor size and smaller and fewer metastatic lesions when injected with cancer cells. These results suggest the existence of a 'vicious cycle' whereby gal-8 secreted by the tumor microenvironment, promotes secretion of chemoattractants at the metastatic niche that promote further recruitment of tumor cells to that site. This study further implicate gal-8 in control of cancer progression and metastasis through its effects on the production of immunoregulatory cytokines.Entities:
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Year: 2020 PMID: 32355198 PMCID: PMC7193594 DOI: 10.1038/s41598-020-64371-z
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379